Canonical Allele Identifier: CA415858922

Gene: CA6

Linked Data

• MyVariant Identifiers: chr1:g.9017338G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8957279G>C , CM000663.2:g.8957279G>C	GRCh38
NC_000001.10:g.9017338G>C , CM000663.1:g.9017338G>C	GRCh37
NC_000001.9:g.8939925G>C	NCBI36
NG_033975.1:g.16446G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377443.7:c.402G>C MANE Select	ENSP00000366662.2:p.Val134=
ENST00000377436.6:c.402G>C	ENSP00000366654.3:p.Val134=
ENST00000377442.3:c.222G>C	ENSP00000366661.2:p.Val74=
ENST00000377443.6:c.402G>C	ENSP00000366662.2:p.Val134=
ENST00000476083.1:n.99-1631G>C
ENST00000549778.5:c.306G>C	ENSP00000447108.1:p.Val102=
NM_001215.3:c.402G>C	NP_001206.2:p.Val134=
NM_001270500.1:c.402G>C	NP_001257429.1:p.Val134=
NM_001270501.1:c.222G>C	NP_001257430.1:p.Val74=
NM_001270502.1:c.25-1631G>C	NP_001257431.1:n.25-1631G>C
XM_011542083.1:c.414G>C	XP_011540385.1:p.Val138=
XM_011542084.1:c.414G>C	XP_011540386.1:p.Val138=
XM_011542083.3:c.414G>C	XP_011540385.1:p.Val138=
XM_011542084.3:c.414G>C	XP_011540386.1:p.Val138=
NM_001215.4:c.402G>C MANE Select	NP_001206.2:p.Val134=
NM_001270500.2:c.402G>C	NP_001257429.1:p.Val134=
NM_001270501.2:c.222G>C	NP_001257430.1:p.Val74=
NM_001270502.2:c.25-1631G>C	NP_001257431.1:n.25-1631G>C