Canonical Allele Identifier: CA885294236

Gene: CLCC1 GPSM2 AKNAD1

Linked Data

• dbSNP Id: rs1391968992
• gnomAD v4: 1-108904011-CTA-C
• MyVariant Identifiers: chr1:g.109446634_109446635del (hg19) ; chr1:g.108904012_108904013del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.108904013_108904014del , CM000663.2:g.108904013_108904014del	GRCh38
NC_000001.10:g.109446635_109446636del , CM000663.1:g.109446635_109446636del	GRCh37
NC_000001.9:g.109248158_109248159del	NCBI36
NG_028108.1:g.32033_32034del
NG_028108.2:g.33664_33665del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690509.1:c.*46-21765_*46-21764del (CLCC1)	ENSP00000510142.1:n.*46-21765_*46-21764del
ENST00000264126.9:c.1063-112_1063-111del (GPSM2) MANE Select	ENSP00000264126.3:n.1063-112_1063-111del
ENST00000357393.6:c.1-54437_1-54436del (AKNAD1)	ENSP00000349968.6:n.1-54437_1-54436del
ENST00000441735.2:c.1063-112_1063-111del (GPSM2)	ENSP00000390629.2:n.1063-112_1063-111del
ENST00000446797.2:c.1063-112_1063-111del (GPSM2)	ENSP00000392138.2:n.1063-112_1063-111del
ENST00000642355.1:c.1063-112_1063-111del (GPSM2)	ENSP00000496104.1:n.1063-112_1063-111del
ENST00000643643.1:c.152-112_152-111del (GPSM2)
ENST00000643921.1:n.66-112_66-111del (GPSM2)
ENST00000645164.2:c.1063-112_1063-111del (GPSM2)	ENSP00000496756.2:n.1063-112_1063-111del
ENST00000645255.1:c.585-112_585-111del (GPSM2)
ENST00000674700.1:c.1006-112_1006-111del (GPSM2)	ENSP00000501743.1:n.1006-112_1006-111del
ENST00000674731.1:c.1006-112_1006-111del (GPSM2)	ENSP00000502401.1:n.1006-112_1006-111del
ENST00000674914.1:c.1114-112_1114-111del (GPSM2)	ENSP00000501579.1:n.1114-112_1114-111del
ENST00000675086.1:c.1063-112_1063-111del (GPSM2)	ENSP00000502476.1:n.1063-112_1063-111del
ENST00000675087.1:c.1114-112_1114-111del (GPSM2)	ENSP00000502020.1:n.1114-112_1114-111del
ENST00000675617.1:n.1625-112_1625-111del (GPSM2)
ENST00000675740.1:n.726_727del (GPSM2)
ENST00000675776.1:n.2336_2337del (GPSM2)
ENST00000676184.1:c.1063-112_1063-111del (GPSM2)	ENSP00000502178.1:n.1063-112_1063-111del
ENST00000676404.1:c.1006-112_1006-111del (GPSM2)	ENSP00000502346.1:n.1006-112_1006-111del
ENST00000264126.7:c.1063-112_1063-111del (GPSM2)	ENSP00000264126.3:n.1063-112_1063-111del
ENST00000357393.5:c.115-54437_115-54436del	ENSP00000349968.5:n.115-54437_115-54436del
ENST00000406462.6:c.1063-112_1063-111del (GPSM2)	ENSP00000385510.1:n.1063-112_1063-111del
NM_013296.4:c.1063-112_1063-111del (GPSM2)	NP_037428.3:n.1063-112_1063-111del
XM_005270787.2:c.1063-112_1063-111del (GPSM2)	XP_005270844.1:n.1063-112_1063-111del
XM_006710589.1:c.1006-112_1006-111del (GPSM2)	XP_006710652.1:n.1006-112_1006-111del
XM_011541301.1:c.1063-112_1063-111del (GPSM2)	XP_011539603.1:n.1063-112_1063-111del
XM_011541302.1:c.1063-112_1063-111del (GPSM2)	XP_011539604.1:n.1063-112_1063-111del
XM_011541303.1:c.1063-112_1063-111del (GPSM2)	XP_011539605.1:n.1063-112_1063-111del
NM_001321038.1:c.1063-112_1063-111del (GPSM2)	NP_001307967.1:n.1063-112_1063-111del
NM_001321039.1:c.1063-112_1063-111del (GPSM2)	NP_001307968.1:n.1063-112_1063-111del
XM_006710589.3:c.1006-112_1006-111del (GPSM2)	XP_006710652.1:n.1006-112_1006-111del
XM_011541301.2:c.1063-112_1063-111del (GPSM2)	XP_011539603.1:n.1063-112_1063-111del
XM_011541302.3:c.1063-112_1063-111del (GPSM2)	XP_011539604.1:n.1063-112_1063-111del
XM_011541303.3:c.1063-112_1063-111del (GPSM2)	XP_011539605.1:n.1063-112_1063-111del
XM_017001097.2:c.1063-112_1063-111del (GPSM2)	XP_016856586.1:n.1063-112_1063-111del
XM_017001098.2:c.1063-112_1063-111del (GPSM2)	XP_016856587.1:n.1063-112_1063-111del
NM_013296.5:c.1063-112_1063-111del (GPSM2) MANE Select	NP_037428.3:n.1063-112_1063-111del
NM_001321038.2:c.1063-112_1063-111del (GPSM2)	NP_001307967.1:n.1063-112_1063-111del
NM_001321039.2:c.1063-112_1063-111del (GPSM2)	NP_001307968.1:n.1063-112_1063-111del
NM_001321039.3:c.1063-112_1063-111del (GPSM2)	NP_001307968.1:n.1063-112_1063-111del