Canonical Allele Identifier: CA740063294

Gene: CA6

Linked Data

• dbSNP Id: rs1373597688
• MyVariant Identifiers: chr1:g.9017057T>A (hg19) ; chr1:g.8956998T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8956998T>A , CM000663.2:g.8956998T>A	GRCh38
NC_000001.10:g.9017057T>A , CM000663.1:g.9017057T>A	GRCh37
NC_000001.9:g.8939644T>A	NCBI36
NG_033975.1:g.16165T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377443.7:c.260-139T>A MANE Select	ENSP00000366662.2:n.260-139T>A
ENST00000377436.6:c.260-139T>A	ENSP00000366654.3:n.260-139T>A
ENST00000377442.3:c.80-139T>A	ENSP00000366661.2:n.80-139T>A
ENST00000377443.6:c.260-139T>A	ENSP00000366662.2:n.260-139T>A
ENST00000476083.1:n.99-1912T>A
ENST00000549778.5:c.169-144T>A	ENSP00000447108.1:n.169-144T>A
NM_001215.3:c.260-139T>A	NP_001206.2:n.260-139T>A
NM_001270500.1:c.260-139T>A	NP_001257429.1:n.260-139T>A
NM_001270501.1:c.80-139T>A	NP_001257430.1:n.80-139T>A
NM_001270502.1:c.25-1912T>A	NP_001257431.1:n.25-1912T>A
XM_011542083.1:c.272-139T>A	XP_011540385.1:n.272-139T>A
XM_011542084.1:c.272-139T>A	XP_011540386.1:n.272-139T>A
XM_011542083.3:c.272-139T>A	XP_011540385.1:n.272-139T>A
XM_011542084.3:c.272-139T>A	XP_011540386.1:n.272-139T>A
NM_001215.4:c.260-139T>A MANE Select	NP_001206.2:n.260-139T>A
NM_001270500.2:c.260-139T>A	NP_001257429.1:n.260-139T>A
NM_001270501.2:c.80-139T>A	NP_001257430.1:n.80-139T>A
NM_001270502.2:c.25-1912T>A	NP_001257431.1:n.25-1912T>A