Canonical Allele Identifier: CA1187885120

Gene: CLCC1 GPSM2 AKNAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.108914818_108914819delinsTC , CM000663.2:g.108914818_108914819delinsTC	GRCh38
NC_000001.10:g.109457440_109457441delinsTC , CM000663.1:g.109457440_109457441delinsTC	GRCh37
NC_000001.9:g.109258963_109258964delinsTC	NCBI36
NG_028108.1:g.42838_42839delinsTC
NG_028108.2:g.44469_44470delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690509.1:c.*45+19806_*45+19807delinsGA (CLCC1)	ENSP00000510142.1:n.*45+19806_*45+19807delinsGA
ENST00000264126.9:c.1263+410_1263+411delinsTC (GPSM2) MANE Select	ENSP00000264126.3:n.1263+410_1263+411delinsTC
ENST00000357393.6:c.-1+48542_-1+48543delinsGA (AKNAD1)	ENSP00000349968.6:n.-1+48542_-1+48543delinsGA
ENST00000441735.2:c.1263+410_1263+411delinsTC (GPSM2)	ENSP00000390629.2:n.1263+410_1263+411delinsTC
ENST00000446797.2:c.1263+410_1263+411delinsTC (GPSM2)	ENSP00000392138.2:n.1263+410_1263+411delinsTC
ENST00000642355.1:c.1263+410_1263+411delinsTC (GPSM2)	ENSP00000496104.1:n.1263+410_1263+411delinsTC
ENST00000643643.1:c.352+410_352+411delinsTC (GPSM2)
ENST00000645164.2:c.1263+410_1263+411delinsTC (GPSM2)	ENSP00000496756.2:n.1263+410_1263+411delinsTC
ENST00000674700.1:c.1206+410_1206+411delinsTC (GPSM2)	ENSP00000501743.1:n.1206+410_1206+411delinsTC
ENST00000674731.1:c.1136-3795_1136-3794delinsTC (GPSM2)	ENSP00000502401.1:n.1136-3795_1136-3794delinsTC
ENST00000674914.1:c.1314+410_1314+411delinsTC (GPSM2)	ENSP00000501579.1:n.1314+410_1314+411delinsTC
ENST00000675086.1:c.1263+410_1263+411delinsTC (GPSM2)	ENSP00000502476.1:n.1263+410_1263+411delinsTC
ENST00000675087.1:c.1314+410_1314+411delinsTC (GPSM2)	ENSP00000502020.1:n.1314+410_1314+411delinsTC
ENST00000675617.1:n.2016_2017delinsTC (GPSM2)
ENST00000675740.1:n.1038+410_1038+411delinsTC (GPSM2)
ENST00000676184.1:c.1263+410_1263+411delinsTC (GPSM2)	ENSP00000502178.1:n.1263+410_1263+411delinsTC
ENST00000676404.1:c.1206+410_1206+411delinsTC (GPSM2)	ENSP00000502346.1:n.1206+410_1206+411delinsTC
ENST00000264126.7:c.1263+410_1263+411delinsTC (GPSM2)	ENSP00000264126.3:n.1263+410_1263+411delinsTC
ENST00000357393.5:c.114+48542_114+48543delinsGA	ENSP00000349968.5:n.114+48542_114+48543delinsGA
ENST00000406462.6:c.1263+410_1263+411delinsTC (GPSM2)	ENSP00000385510.1:n.1263+410_1263+411delinsTC
ENST00000441735.1:c.32+410_32+411delinsTC (GPSM2)
NM_013296.4:c.1263+410_1263+411delinsTC (GPSM2)	NP_037428.3:n.1263+410_1263+411delinsTC
XM_005270787.2:c.1263+410_1263+411delinsTC (GPSM2)	XP_005270844.1:n.1263+410_1263+411delinsTC
XM_006710589.1:c.1206+410_1206+411delinsTC (GPSM2)	XP_006710652.1:n.1206+410_1206+411delinsTC
XM_011541301.1:c.1263+410_1263+411delinsTC (GPSM2)	XP_011539603.1:n.1263+410_1263+411delinsTC
XM_011541302.1:c.1263+410_1263+411delinsTC (GPSM2)	XP_011539604.1:n.1263+410_1263+411delinsTC
XM_011541303.1:c.1263+410_1263+411delinsTC (GPSM2)	XP_011539605.1:n.1263+410_1263+411delinsTC
NM_001321038.1:c.1263+410_1263+411delinsTC (GPSM2)	NP_001307967.1:n.1263+410_1263+411delinsTC
NM_001321039.1:c.1263+410_1263+411delinsTC (GPSM2)	NP_001307968.1:n.1263+410_1263+411delinsTC
XM_006710589.3:c.1206+410_1206+411delinsTC (GPSM2)	XP_006710652.1:n.1206+410_1206+411delinsTC
XM_011541301.2:c.1263+410_1263+411delinsTC (GPSM2)	XP_011539603.1:n.1263+410_1263+411delinsTC
XM_011541302.3:c.1263+410_1263+411delinsTC (GPSM2)	XP_011539604.1:n.1263+410_1263+411delinsTC
XM_011541303.3:c.1263+410_1263+411delinsTC (GPSM2)	XP_011539605.1:n.1263+410_1263+411delinsTC
XM_017001097.2:c.1263+410_1263+411delinsTC (GPSM2)	XP_016856586.1:n.1263+410_1263+411delinsTC
XM_017001098.2:c.1263+410_1263+411delinsTC (GPSM2)	XP_016856587.1:n.1263+410_1263+411delinsTC
NM_013296.5:c.1263+410_1263+411delinsTC (GPSM2) MANE Select	NP_037428.3:n.1263+410_1263+411delinsTC
NM_001321038.2:c.1263+410_1263+411delinsTC (GPSM2)	NP_001307967.1:n.1263+410_1263+411delinsTC
NM_001321039.2:c.1263+410_1263+411delinsTC (GPSM2)	NP_001307968.1:n.1263+410_1263+411delinsTC
NM_001321039.3:c.1263+410_1263+411delinsTC (GPSM2)	NP_001307968.1:n.1263+410_1263+411delinsTC