Canonical Allele Identifier: CA338184654

Gene: CA6

Linked Data

• MyVariant Identifiers: chr1:g.9017210C>A (hg19) ; chr1:g.8957151C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8957151C>A , CM000663.2:g.8957151C>A	GRCh38
NC_000001.10:g.9017210C>A , CM000663.1:g.9017210C>A	GRCh37
NC_000001.9:g.8939797C>A	NCBI36
NG_033975.1:g.16318C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000377443.7:c.274C>A MANE Select	ENSP00000366662.2:p.Pro92Thr
ENST00000377436.6:c.274C>A	ENSP00000366654.3:p.Pro92Thr
ENST00000377442.3:c.94C>A	ENSP00000366661.2:p.Pro32Thr
ENST00000377443.6:c.274C>A	ENSP00000366662.2:p.Pro92Thr
ENST00000476083.1:n.99-1759C>A
ENST00000549778.5:c.178C>A	ENSP00000447108.1:p.Pro60Thr
NM_001215.3:c.274C>A	NP_001206.2:p.Pro92Thr
NM_001270500.1:c.274C>A	NP_001257429.1:p.Pro92Thr
NM_001270501.1:c.94C>A	NP_001257430.1:p.Pro32Thr
NM_001270502.1:c.25-1759C>A	NP_001257431.1:n.25-1759C>A
XM_011542083.1:c.286C>A	XP_011540385.1:p.Pro96Thr
XM_011542084.1:c.286C>A	XP_011540386.1:p.Pro96Thr
XM_011542083.3:c.286C>A	XP_011540385.1:p.Pro96Thr
XM_011542084.3:c.286C>A	XP_011540386.1:p.Pro96Thr
NM_001215.4:c.274C>A MANE Select	NP_001206.2:p.Pro92Thr
NM_001270500.2:c.274C>A	NP_001257429.1:p.Pro92Thr
NM_001270501.2:c.94C>A	NP_001257430.1:p.Pro32Thr
NM_001270502.2:c.25-1759C>A	NP_001257431.1:n.25-1759C>A