Canonical Allele Identifier: CA2526699095

Gene: CLCC1 GPSM2 AKNAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.108904026_108904027insGGAATCATACTAAGTA , CM000663.2:g.108904026_108904027insGGAATCATACTAAGTA	GRCh38
NC_000001.10:g.109446648_109446649insGGAATCATACTAAGTA , CM000663.1:g.109446648_109446649insGGAATCATACTAAGTA	GRCh37
NC_000001.9:g.109248171_109248172insGGAATCATACTAAGTA	NCBI36
NG_028108.1:g.32046_32047insGGAATCATACTAAGTA
NG_028108.2:g.33677_33678insGGAATCATACTAAGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690509.1:c.*46-21779_*46-21778insTACTTAGTATGATTCC (CLCC1)	ENSP00000510142.1:n.*46-21779_*46-21778insTACTTAGTATGATTCC
ENST00000264126.9:c.1063-99_1063-98insGGAATCATACTAAGTA (GPSM2) MANE Select	ENSP00000264126.3:n.1063-99_1063-98insGGAATCATACTAAGTA
ENST00000357393.6:c.1-54451_1-54450insTACTTAGTATGATTCC (AKNAD1)	ENSP00000349968.6:n.1-54451_1-54450insTACTTAGTATGATTCC
ENST00000441735.2:c.1063-99_1063-98insGGAATCATACTAAGTA (GPSM2)	ENSP00000390629.2:n.1063-99_1063-98insGGAATCATACTAAGTA
ENST00000446797.2:c.1063-99_1063-98insGGAATCATACTAAGTA (GPSM2)	ENSP00000392138.2:n.1063-99_1063-98insGGAATCATACTAAGTA
ENST00000642355.1:c.1063-99_1063-98insGGAATCATACTAAGTA (GPSM2)	ENSP00000496104.1:n.1063-99_1063-98insGGAATCATACTAAGTA
ENST00000643643.1:c.152-99_152-98insGGAATCATACTAAGTA (GPSM2)
ENST00000643921.1:n.66-99_66-98insGGAATCATACTAAGTA (GPSM2)
ENST00000645164.2:c.1063-99_1063-98insGGAATCATACTAAGTA (GPSM2)	ENSP00000496756.2:n.1063-99_1063-98insGGAATCATACTAAGTA
ENST00000645255.1:c.585-99_585-98insGGAATCATACTAAGTA (GPSM2)
ENST00000674700.1:c.1006-99_1006-98insGGAATCATACTAAGTA (GPSM2)	ENSP00000501743.1:n.1006-99_1006-98insGGAATCATACTAAGTA
ENST00000674731.1:c.1006-99_1006-98insGGAATCATACTAAGTA (GPSM2)	ENSP00000502401.1:n.1006-99_1006-98insGGAATCATACTAAGTA
ENST00000674914.1:c.1114-99_1114-98insGGAATCATACTAAGTA (GPSM2)	ENSP00000501579.1:n.1114-99_1114-98insGGAATCATACTAAGTA
ENST00000675086.1:c.1063-99_1063-98insGGAATCATACTAAGTA (GPSM2)	ENSP00000502476.1:n.1063-99_1063-98insGGAATCATACTAAGTA
ENST00000675087.1:c.1114-99_1114-98insGGAATCATACTAAGTA (GPSM2)	ENSP00000502020.1:n.1114-99_1114-98insGGAATCATACTAAGTA
ENST00000675617.1:n.1625-99_1625-98insGGAATCATACTAAGTA (GPSM2)
ENST00000675740.1:n.739_740insGGAATCATACTAAGTA (GPSM2)
ENST00000675776.1:n.2349_2350insGGAATCATACTAAGTA (GPSM2)
ENST00000676184.1:c.1063-99_1063-98insGGAATCATACTAAGTA (GPSM2)	ENSP00000502178.1:n.1063-99_1063-98insGGAATCATACTAAGTA
ENST00000676404.1:c.1006-99_1006-98insGGAATCATACTAAGTA (GPSM2)	ENSP00000502346.1:n.1006-99_1006-98insGGAATCATACTAAGTA
ENST00000264126.7:c.1063-99_1063-98insGGAATCATACTAAGTA (GPSM2)	ENSP00000264126.3:n.1063-99_1063-98insGGAATCATACTAAGTA
ENST00000357393.5:c.115-54451_115-54450insTACTTAGTATGATTCC	ENSP00000349968.5:n.115-54451_115-54450insTACTTAGTATGATTCC
ENST00000406462.6:c.1063-99_1063-98insGGAATCATACTAAGTA (GPSM2)	ENSP00000385510.1:n.1063-99_1063-98insGGAATCATACTAAGTA
NM_013296.4:c.1063-99_1063-98insGGAATCATACTAAGTA (GPSM2)	NP_037428.3:n.1063-99_1063-98insGGAATCATACTAAGTA
XM_005270787.2:c.1063-99_1063-98insGGAATCATACTAAGTA (GPSM2)	XP_005270844.1:n.1063-99_1063-98insGGAATCATACTAAGTA
XM_006710589.1:c.1006-99_1006-98insGGAATCATACTAAGTA (GPSM2)	XP_006710652.1:n.1006-99_1006-98insGGAATCATACTAAGTA
XM_011541301.1:c.1063-99_1063-98insGGAATCATACTAAGTA (GPSM2)	XP_011539603.1:n.1063-99_1063-98insGGAATCATACTAAGTA
XM_011541302.1:c.1063-99_1063-98insGGAATCATACTAAGTA (GPSM2)	XP_011539604.1:n.1063-99_1063-98insGGAATCATACTAAGTA
XM_011541303.1:c.1063-99_1063-98insGGAATCATACTAAGTA (GPSM2)	XP_011539605.1:n.1063-99_1063-98insGGAATCATACTAAGTA
NM_001321038.1:c.1063-99_1063-98insGGAATCATACTAAGTA (GPSM2)	NP_001307967.1:n.1063-99_1063-98insGGAATCATACTAAGTA
NM_001321039.1:c.1063-99_1063-98insGGAATCATACTAAGTA (GPSM2)	NP_001307968.1:n.1063-99_1063-98insGGAATCATACTAAGTA
XM_006710589.3:c.1006-99_1006-98insGGAATCATACTAAGTA (GPSM2)	XP_006710652.1:n.1006-99_1006-98insGGAATCATACTAAGTA
XM_011541301.2:c.1063-99_1063-98insGGAATCATACTAAGTA (GPSM2)	XP_011539603.1:n.1063-99_1063-98insGGAATCATACTAAGTA
XM_011541302.3:c.1063-99_1063-98insGGAATCATACTAAGTA (GPSM2)	XP_011539604.1:n.1063-99_1063-98insGGAATCATACTAAGTA
XM_011541303.3:c.1063-99_1063-98insGGAATCATACTAAGTA (GPSM2)	XP_011539605.1:n.1063-99_1063-98insGGAATCATACTAAGTA
XM_017001097.2:c.1063-99_1063-98insGGAATCATACTAAGTA (GPSM2)	XP_016856586.1:n.1063-99_1063-98insGGAATCATACTAAGTA
XM_017001098.2:c.1063-99_1063-98insGGAATCATACTAAGTA (GPSM2)	XP_016856587.1:n.1063-99_1063-98insGGAATCATACTAAGTA
NM_013296.5:c.1063-99_1063-98insGGAATCATACTAAGTA (GPSM2) MANE Select	NP_037428.3:n.1063-99_1063-98insGGAATCATACTAAGTA
NM_001321038.2:c.1063-99_1063-98insGGAATCATACTAAGTA (GPSM2)	NP_001307967.1:n.1063-99_1063-98insGGAATCATACTAAGTA
NM_001321039.2:c.1063-99_1063-98insGGAATCATACTAAGTA (GPSM2)	NP_001307968.1:n.1063-99_1063-98insGGAATCATACTAAGTA
NM_001321039.3:c.1063-99_1063-98insGGAATCATACTAAGTA (GPSM2)	NP_001307968.1:n.1063-99_1063-98insGGAATCATACTAAGTA