Canonical Allele Identifier: CA17706559

Gene: CA6

Linked Data

• dbSNP Id: rs1043189950
• gnomAD v3: 1-8957055-T-G
• gnomAD v4: 1-8957055-T-G
• MyVariant Identifiers: chr1:g.9017114T>G (hg19) ; chr1:g.8957055T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8957055T>G , CM000663.2:g.8957055T>G	GRCh38
NC_000001.10:g.9017114T>G , CM000663.1:g.9017114T>G	GRCh37
NC_000001.9:g.8939701T>G	NCBI36
NG_033975.1:g.16222T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377443.7:c.260-82T>G MANE Select	ENSP00000366662.2:n.260-82T>G
ENST00000377436.6:c.260-82T>G	ENSP00000366654.3:n.260-82T>G
ENST00000377442.3:c.80-82T>G	ENSP00000366661.2:n.80-82T>G
ENST00000377443.6:c.260-82T>G	ENSP00000366662.2:n.260-82T>G
ENST00000476083.1:n.99-1855T>G
ENST00000549778.5:c.169-87T>G	ENSP00000447108.1:n.169-87T>G
NM_001215.3:c.260-82T>G	NP_001206.2:n.260-82T>G
NM_001270500.1:c.260-82T>G	NP_001257429.1:n.260-82T>G
NM_001270501.1:c.80-82T>G	NP_001257430.1:n.80-82T>G
NM_001270502.1:c.25-1855T>G	NP_001257431.1:n.25-1855T>G
XM_011542083.1:c.272-82T>G	XP_011540385.1:n.272-82T>G
XM_011542084.1:c.272-82T>G	XP_011540386.1:n.272-82T>G
XM_011542083.3:c.272-82T>G	XP_011540385.1:n.272-82T>G
XM_011542084.3:c.272-82T>G	XP_011540386.1:n.272-82T>G
NM_001215.4:c.260-82T>G MANE Select	NP_001206.2:n.260-82T>G
NM_001270500.2:c.260-82T>G	NP_001257429.1:n.260-82T>G
NM_001270501.2:c.80-82T>G	NP_001257430.1:n.80-82T>G
NM_001270502.2:c.25-1855T>G	NP_001257431.1:n.25-1855T>G