Canonical Allele Identifier: CA1139925299

Gene: CA6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8949347C= , CM000663.2:g.8949347C=	GRCh38
NC_000001.10:g.9009406C= , CM000663.1:g.9009406C=	GRCh37
NC_000001.9:g.8931993C=	NCBI36
NG_033975.1:g.8514C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377443.7:c.164C= MANE Select	ENSP00000366662.2:p.Thr55=
ENST00000377436.6:c.164C=	ENSP00000366654.3:p.Thr55=
ENST00000377442.3:c.79+3382C=	ENSP00000366661.2:n.79+3382C=
ENST00000377443.6:c.164C=	ENSP00000366662.2:p.Thr55=
ENST00000476083.1:n.98+3382C=
ENST00000480186.7:c.164C=	ENSP00000435280.1:p.Thr55=
ENST00000549778.5:c.164C=	ENSP00000447108.1:p.Thr55=
NM_001215.3:c.164C=	NP_001206.2:p.Thr55=
NM_001270500.1:c.164C=	NP_001257429.1:p.Thr55=
NM_001270501.1:c.79+3382C=	NP_001257430.1:n.79+3382C=
NM_001270502.1:c.24+3382C=	NP_001257431.1:n.24+3382C=
XM_011542083.1:c.176C=	XP_011540385.1:p.Thr59=
XM_011542084.1:c.176C=	XP_011540386.1:p.Thr59=
XM_011542083.3:c.176C=	XP_011540385.1:p.Thr59=
XM_011542084.3:c.176C=	XP_011540386.1:p.Thr59=
NM_001215.4:c.164C= MANE Select	NP_001206.2:p.Thr55=
NM_001270500.2:c.164C=	NP_001257429.1:p.Thr55=
NM_001270501.2:c.79+3382C=	NP_001257430.1:n.79+3382C=
NM_001270502.2:c.24+3382C=	NP_001257431.1:n.24+3382C=