Canonical Allele Identifier: CA2646885217

Gene: CLCC1 GPSM2 AKNAD1

Linked Data

• gnomAD v4: 1-108923965-TTTTTTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.108923966_108923971del , CM000663.2:g.108923966_108923971del	GRCh38
NC_000001.10:g.109466588_109466593del , CM000663.1:g.109466588_109466593del	GRCh37
NC_000001.9:g.109268111_109268116del	NCBI36
NG_028108.1:g.51986_51991del
NG_028108.2:g.53617_53622del

Transcript Alleles

HGVS	Amino-acid change
ENST00000690509.1:c.*45+10654_*45+10659del (CLCC1)	ENSP00000510142.1:n.*45+10654_*45+10659de...
ENST00000264126.9:c.1601-34_1601-29del (GPSM2) MANE Select	ENSP00000264126.3:n.1601-34_1601-29del
ENST00000357393.6:c.-1+39390_-1+39395del (AKNAD1)	ENSP00000349968.6:n.-1+39390_-1+39395del
ENST00000441735.2:c.1601-34_1601-29del (GPSM2)	ENSP00000390629.2:n.1601-34_1601-29del
ENST00000446797.2:c.1601-34_1601-29del (GPSM2)	ENSP00000392138.2:n.1601-34_1601-29del
ENST00000642355.1:c.1601-34_1601-29del (GPSM2)	ENSP00000496104.1:n.1601-34_1601-29del
ENST00000643643.1:c.690-34_690-29del (GPSM2)
ENST00000645164.2:c.1601-34_1601-29del (GPSM2)	ENSP00000496756.2:n.1601-34_1601-29del
ENST00000674700.1:c.1543+1390_1543+1395del (GPSM2)	ENSP00000501743.1:n.1543+1390_1543+1395de...
ENST00000674731.1:c.*318-34_*318-29del (GPSM2)	ENSP00000502401.1:n.*318-34_*318-29del
ENST00000674914.1:c.1652-34_1652-29del (GPSM2)	ENSP00000501579.1:n.1652-34_1652-29del
ENST00000675086.1:c.1424-34_1424-29del (GPSM2)	ENSP00000502476.1:n.1424-34_1424-29del
ENST00000675087.1:c.1652-34_1652-29del (GPSM2)	ENSP00000502020.1:n.1652-34_1652-29del
ENST00000675740.1:n.1216-34_1216-29del (GPSM2)
ENST00000676184.1:c.1601-34_1601-29del (GPSM2)	ENSP00000502178.1:n.1601-34_1601-29del
ENST00000676404.1:c.*507-34_*507-29del (GPSM2)	ENSP00000502346.1:n.*507-34_*507-29del
ENST00000264126.7:c.1601-34_1601-29del (GPSM2)	ENSP00000264126.3:n.1601-34_1601-29del
ENST00000357393.5:c.114+39390_114+39395del	ENSP00000349968.5:n.114+39390_114+39395de...
ENST00000406462.6:c.1601-34_1601-29del (GPSM2)	ENSP00000385510.1:n.1601-34_1601-29del
ENST00000441735.1:c.370-34_370-29del (GPSM2)
NM_013296.4:c.1601-34_1601-29del (GPSM2)	NP_037428.3:n.1601-34_1601-29del
XM_005270787.2:c.1601-34_1601-29del (GPSM2)	XP_005270844.1:n.1601-34_1601-29del
XM_006710589.1:c.1544-34_1544-29del (GPSM2)	XP_006710652.1:n.1544-34_1544-29del
XM_011541301.1:c.1601-34_1601-29del (GPSM2)	XP_011539603.1:n.1601-34_1601-29del
XM_011541302.1:c.1601-34_1601-29del (GPSM2)	XP_011539604.1:n.1601-34_1601-29del
NM_001321038.1:c.1601-34_1601-29del (GPSM2)	NP_001307967.1:n.1601-34_1601-29del
NM_001321039.1:c.1601-34_1601-29del (GPSM2)	NP_001307968.1:n.1601-34_1601-29del
XM_006710589.3:c.1544-34_1544-29del (GPSM2)	XP_006710652.1:n.1544-34_1544-29del
XM_011541301.2:c.1601-34_1601-29del (GPSM2)	XP_011539603.1:n.1601-34_1601-29del
XM_011541302.3:c.1601-34_1601-29del (GPSM2)	XP_011539604.1:n.1601-34_1601-29del
XM_017001097.2:c.1601-34_1601-29del (GPSM2)	XP_016856586.1:n.1601-34_1601-29del
XM_017001098.2:c.1601-34_1601-29del (GPSM2)	XP_016856587.1:n.1601-34_1601-29del
NM_013296.5:c.1601-34_1601-29del (GPSM2) MANE Select	NP_037428.3:n.1601-34_1601-29del
NM_001321038.2:c.1601-34_1601-29del (GPSM2)	NP_001307967.1:n.1601-34_1601-29del
NM_001321039.2:c.1601-34_1601-29del (GPSM2)	NP_001307968.1:n.1601-34_1601-29del
NM_001321039.3:c.1601-34_1601-29del (GPSM2)	NP_001307968.1:n.1601-34_1601-29del