Canonical Allele Identifier: CA1187889021

Gene: CLCC1 GPSM2 AKNAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.108923958_108923961delinsTTTG , CM000663.2:g.108923958_108923961delinsTTTG	GRCh38
NC_000001.10:g.109466580_109466583delinsTTTG , CM000663.1:g.109466580_109466583delinsTTTG	GRCh37
NC_000001.9:g.109268103_109268106delinsTTTG	NCBI36
NG_028108.1:g.51978_51981delinsTTTG
NG_028108.2:g.53609_53612delinsTTTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000690509.1:c.*45+10664_*45+10667delinsCAAA (CLCC1)	ENSP00000510142.1:n.*45+10664_*45+10667de...
ENST00000264126.9:c.1601-42_1601-39delinsTTTG (GPSM2) MANE Select	ENSP00000264126.3:n.1601-42_1601-39delins...
ENST00000357393.6:c.-1+39400_-1+39403delinsCAAA (AKNAD1)	ENSP00000349968.6:n.-1+39400_-1+39403deli...
ENST00000441735.2:c.1601-42_1601-39delinsTTTG (GPSM2)	ENSP00000390629.2:n.1601-42_1601-39delins...
ENST00000446797.2:c.1601-42_1601-39delinsTTTG (GPSM2)	ENSP00000392138.2:n.1601-42_1601-39delins...
ENST00000642355.1:c.1601-42_1601-39delinsTTTG (GPSM2)	ENSP00000496104.1:n.1601-42_1601-39delins...
ENST00000643643.1:c.690-42_690-39delinsTTTG (GPSM2)
ENST00000645164.2:c.1601-42_1601-39delinsTTTG (GPSM2)	ENSP00000496756.2:n.1601-42_1601-39delins...
ENST00000674700.1:c.1543+1382_1543+1385delinsTTTG (GPSM2)	ENSP00000501743.1:n.1543+1382_1543+1385de...
ENST00000674731.1:c.*318-42_*318-39delinsTTTG (GPSM2)	ENSP00000502401.1:n.*318-42_*318-39delins...
ENST00000674914.1:c.1652-42_1652-39delinsTTTG (GPSM2)	ENSP00000501579.1:n.1652-42_1652-39delins...
ENST00000675086.1:c.1424-42_1424-39delinsTTTG (GPSM2)	ENSP00000502476.1:n.1424-42_1424-39delins...
ENST00000675087.1:c.1652-42_1652-39delinsTTTG (GPSM2)	ENSP00000502020.1:n.1652-42_1652-39delins...
ENST00000675740.1:n.1216-42_1216-39delinsTTTG (GPSM2)
ENST00000676184.1:c.1601-42_1601-39delinsTTTG (GPSM2)	ENSP00000502178.1:n.1601-42_1601-39delins...
ENST00000676404.1:c.*507-42_*507-39delinsTTTG (GPSM2)	ENSP00000502346.1:n.*507-42_*507-39delins...
ENST00000264126.7:c.1601-42_1601-39delinsTTTG (GPSM2)	ENSP00000264126.3:n.1601-42_1601-39delins...
ENST00000357393.5:c.114+39400_114+39403delinsCAAA	ENSP00000349968.5:n.114+39400_114+39403de...
ENST00000406462.6:c.1601-42_1601-39delinsTTTG (GPSM2)	ENSP00000385510.1:n.1601-42_1601-39delins...
ENST00000441735.1:c.370-42_370-39delinsTTTG (GPSM2)
NM_013296.4:c.1601-42_1601-39delinsTTTG (GPSM2)	NP_037428.3:n.1601-42_1601-39delinsTTTG
XM_005270787.2:c.1601-42_1601-39delinsTTTG (GPSM2)	XP_005270844.1:n.1601-42_1601-39delinsTTT...
XM_006710589.1:c.1544-42_1544-39delinsTTTG (GPSM2)	XP_006710652.1:n.1544-42_1544-39delinsTTT...
XM_011541301.1:c.1601-42_1601-39delinsTTTG (GPSM2)	XP_011539603.1:n.1601-42_1601-39delinsTTT...
XM_011541302.1:c.1601-42_1601-39delinsTTTG (GPSM2)	XP_011539604.1:n.1601-42_1601-39delinsTTT...
NM_001321038.1:c.1601-42_1601-39delinsTTTG (GPSM2)	NP_001307967.1:n.1601-42_1601-39delinsTTT...
NM_001321039.1:c.1601-42_1601-39delinsTTTG (GPSM2)	NP_001307968.1:n.1601-42_1601-39delinsTTT...
XM_006710589.3:c.1544-42_1544-39delinsTTTG (GPSM2)	XP_006710652.1:n.1544-42_1544-39delinsTTT...
XM_011541301.2:c.1601-42_1601-39delinsTTTG (GPSM2)	XP_011539603.1:n.1601-42_1601-39delinsTTT...
XM_011541302.3:c.1601-42_1601-39delinsTTTG (GPSM2)	XP_011539604.1:n.1601-42_1601-39delinsTTT...
XM_017001097.2:c.1601-42_1601-39delinsTTTG (GPSM2)	XP_016856586.1:n.1601-42_1601-39delinsTTT...
XM_017001098.2:c.1601-42_1601-39delinsTTTG (GPSM2)	XP_016856587.1:n.1601-42_1601-39delinsTTT...
NM_013296.5:c.1601-42_1601-39delinsTTTG (GPSM2) MANE Select	NP_037428.3:n.1601-42_1601-39delinsTTTG
NM_001321038.2:c.1601-42_1601-39delinsTTTG (GPSM2)	NP_001307967.1:n.1601-42_1601-39delinsTTT...
NM_001321039.2:c.1601-42_1601-39delinsTTTG (GPSM2)	NP_001307968.1:n.1601-42_1601-39delinsTTT...
NM_001321039.3:c.1601-42_1601-39delinsTTTG (GPSM2)	NP_001307968.1:n.1601-42_1601-39delinsTTT...