Canonical Allele Identifier: CA1187889087

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.108924090C= , CM000663.2:g.108924090C= GRCh38
NC_000001.10:g.109466712C= , CM000663.1:g.109466712C= GRCh37
NC_000001.9:g.109268235C= NCBI36
NG_028108.1:g.52110C=
NG_028108.2:g.53741C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000690509.1:c.*45+10535G= (CLCC1) ENSP00000510142.1:n.*45+10535G=
ENST00000264126.9:c.1691C= (GPSM2) MANE Select ENSP00000264126.3:p.Ala564=
ENST00000357393.6:c.-1+39271G= (AKNAD1) ENSP00000349968.6:n.-1+39271G=
ENST00000441735.2:c.1691C= (GPSM2) ENSP00000390629.2:p.Ala564=
ENST00000446797.2:c.1691C= (GPSM2) ENSP00000392138.2:p.Ala564=
ENST00000642355.1:c.1691C= (GPSM2) ENSP00000496104.1:p.Ala564=
ENST00000643643.1:c.780C= (GPSM2)
ENST00000645164.2:c.1691C= (GPSM2) ENSP00000496756.2:p.Ala564=
ENST00000674700.1:c.1543+1514C= (GPSM2) ENSP00000501743.1:n.1543+1514C=
ENST00000674731.1:c.*408C= (GPSM2) ENSP00000502401.1:n.*408C=
ENST00000674914.1:c.1742C= (GPSM2) ENSP00000501579.1:p.Ala581=
ENST00000675086.1:c.1514C= (GPSM2) ENSP00000502476.1:p.Ala505=
ENST00000675087.1:c.1742C= (GPSM2) ENSP00000502020.1:p.Ala581=
ENST00000675740.1:n.1306C= (GPSM2)
ENST00000676184.1:c.1691C= (GPSM2) ENSP00000502178.1:p.Ala564=
ENST00000676404.1:c.*597C= (GPSM2) ENSP00000502346.1:n.*597C=
ENST00000264126.7:c.1691C= (GPSM2) ENSP00000264126.3:p.Ala564=
ENST00000357393.5:c.114+39271G= ENSP00000349968.5:n.114+39271G=
ENST00000406462.6:c.1691C= (GPSM2) ENSP00000385510.1:p.Ala564=
ENST00000441735.1:c.460C= (GPSM2)
NM_013296.4:c.1691C= (GPSM2) NP_037428.3:p.Ala564=
XM_005270787.2:c.1691C= (GPSM2) XP_005270844.1:p.Ala564=
XM_006710589.1:c.1634C= (GPSM2) XP_006710652.1:p.Ala545=
XM_011541301.1:c.1691C= (GPSM2) XP_011539603.1:p.Ala564=
XM_011541302.1:c.1691C= (GPSM2) XP_011539604.1:p.Ala564=
NM_001321038.1:c.1691C= (GPSM2) NP_001307967.1:p.Ala564=
NM_001321039.1:c.1691C= (GPSM2) NP_001307968.1:p.Ala564=
XM_006710589.3:c.1634C= (GPSM2) XP_006710652.1:p.Ala545=
XM_011541301.2:c.1691C= (GPSM2) XP_011539603.1:p.Ala564=
XM_011541302.3:c.1691C= (GPSM2) XP_011539604.1:p.Ala564=
XM_017001097.2:c.1691C= (GPSM2) XP_016856586.1:p.Ala564=
XM_017001098.2:c.1691C= (GPSM2) XP_016856587.1:p.Ala564=
NM_013296.5:c.1691C= (GPSM2) MANE Select NP_037428.3:p.Ala564=
NM_001321038.2:c.1691C= (GPSM2) NP_001307967.1:p.Ala564=
NM_001321039.2:c.1691C= (GPSM2) NP_001307968.1:p.Ala564=
NM_001321039.3:c.1691C= (GPSM2) NP_001307968.1:p.Ala564=