Canonical Allele Identifier: CA885320428

Gene: CLCC1 GPSM2 AKNAD1

Linked Data

• dbSNP Id: rs1338220796
• gnomAD v4: 1-108923947-GTTTT-G
• MyVariant Identifiers: chr1:g.109466570_109466573del (hg19) ; chr1:g.108923948_108923951del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.108923950_108923953del , CM000663.2:g.108923950_108923953del	GRCh38
NC_000001.10:g.109466572_109466575del , CM000663.1:g.109466572_109466575del	GRCh37
NC_000001.9:g.109268095_109268098del	NCBI36
NG_028108.1:g.51970_51973del
NG_028108.2:g.53601_53604del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690509.1:c.*45+10674_*45+10677del (CLCC1)	ENSP00000510142.1:n.*45+10674_*45+10677del
ENST00000264126.9:c.1601-50_1601-47del (GPSM2) MANE Select	ENSP00000264126.3:n.1601-50_1601-47del
ENST00000357393.6:c.-1+39410_-1+39413del (AKNAD1)	ENSP00000349968.6:n.-1+39410_-1+39413del
ENST00000441735.2:c.1601-50_1601-47del (GPSM2)	ENSP00000390629.2:n.1601-50_1601-47del
ENST00000446797.2:c.1601-50_1601-47del (GPSM2)	ENSP00000392138.2:n.1601-50_1601-47del
ENST00000642355.1:c.1601-50_1601-47del (GPSM2)	ENSP00000496104.1:n.1601-50_1601-47del
ENST00000643643.1:c.690-50_690-47del (GPSM2)
ENST00000645164.2:c.1601-50_1601-47del (GPSM2)	ENSP00000496756.2:n.1601-50_1601-47del
ENST00000674700.1:c.1543+1374_1543+1377del (GPSM2)	ENSP00000501743.1:n.1543+1374_1543+1377del
ENST00000674731.1:c.*318-50_*318-47del (GPSM2)	ENSP00000502401.1:n.*318-50_*318-47del
ENST00000674914.1:c.1652-50_1652-47del (GPSM2)	ENSP00000501579.1:n.1652-50_1652-47del
ENST00000675086.1:c.1424-50_1424-47del (GPSM2)	ENSP00000502476.1:n.1424-50_1424-47del
ENST00000675087.1:c.1652-50_1652-47del (GPSM2)	ENSP00000502020.1:n.1652-50_1652-47del
ENST00000675740.1:n.1216-50_1216-47del (GPSM2)
ENST00000676184.1:c.1601-50_1601-47del (GPSM2)	ENSP00000502178.1:n.1601-50_1601-47del
ENST00000676404.1:c.*507-50_*507-47del (GPSM2)	ENSP00000502346.1:n.*507-50_*507-47del
ENST00000264126.7:c.1601-50_1601-47del (GPSM2)	ENSP00000264126.3:n.1601-50_1601-47del
ENST00000357393.5:c.114+39410_114+39413del	ENSP00000349968.5:n.114+39410_114+39413del
ENST00000406462.6:c.1601-50_1601-47del (GPSM2)	ENSP00000385510.1:n.1601-50_1601-47del
ENST00000441735.1:c.370-50_370-47del (GPSM2)
NM_013296.4:c.1601-50_1601-47del (GPSM2)	NP_037428.3:n.1601-50_1601-47del
XM_005270787.2:c.1601-50_1601-47del (GPSM2)	XP_005270844.1:n.1601-50_1601-47del
XM_006710589.1:c.1544-50_1544-47del (GPSM2)	XP_006710652.1:n.1544-50_1544-47del
XM_011541301.1:c.1601-50_1601-47del (GPSM2)	XP_011539603.1:n.1601-50_1601-47del
XM_011541302.1:c.1601-50_1601-47del (GPSM2)	XP_011539604.1:n.1601-50_1601-47del
NM_001321038.1:c.1601-50_1601-47del (GPSM2)	NP_001307967.1:n.1601-50_1601-47del
NM_001321039.1:c.1601-50_1601-47del (GPSM2)	NP_001307968.1:n.1601-50_1601-47del
XM_006710589.3:c.1544-50_1544-47del (GPSM2)	XP_006710652.1:n.1544-50_1544-47del
XM_011541301.2:c.1601-50_1601-47del (GPSM2)	XP_011539603.1:n.1601-50_1601-47del
XM_011541302.3:c.1601-50_1601-47del (GPSM2)	XP_011539604.1:n.1601-50_1601-47del
XM_017001097.2:c.1601-50_1601-47del (GPSM2)	XP_016856586.1:n.1601-50_1601-47del
XM_017001098.2:c.1601-50_1601-47del (GPSM2)	XP_016856587.1:n.1601-50_1601-47del
NM_013296.5:c.1601-50_1601-47del (GPSM2) MANE Select	NP_037428.3:n.1601-50_1601-47del
NM_001321038.2:c.1601-50_1601-47del (GPSM2)	NP_001307967.1:n.1601-50_1601-47del
NM_001321039.2:c.1601-50_1601-47del (GPSM2)	NP_001307968.1:n.1601-50_1601-47del
NM_001321039.3:c.1601-50_1601-47del (GPSM2)	NP_001307968.1:n.1601-50_1601-47del