Canonical Allele Identifier: CA338184770

Gene: CA6

Linked Data

• gnomAD v4: 1-8957207-G-A
• MyVariant Identifiers: chr1:g.9017266G>A (hg19) ; chr1:g.8957207G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8957207G>A , CM000663.2:g.8957207G>A	GRCh38
NC_000001.10:g.9017266G>A , CM000663.1:g.9017266G>A	GRCh37
NC_000001.9:g.8939853G>A	NCBI36
NG_033975.1:g.16374G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377443.7:c.330G>A MANE Select	ENSP00000366662.2:p.Met110Ile
ENST00000377436.6:c.330G>A	ENSP00000366654.3:p.Met110Ile
ENST00000377442.3:c.150G>A	ENSP00000366661.2:p.Met50Ile
ENST00000377443.6:c.330G>A	ENSP00000366662.2:p.Met110Ile
ENST00000476083.1:n.99-1703G>A
ENST00000549778.5:c.234G>A	ENSP00000447108.1:p.Met78Ile
NM_001215.3:c.330G>A	NP_001206.2:p.Met110Ile
NM_001270500.1:c.330G>A	NP_001257429.1:p.Met110Ile
NM_001270501.1:c.150G>A	NP_001257430.1:p.Met50Ile
NM_001270502.1:c.25-1703G>A	NP_001257431.1:n.25-1703G>A
XM_011542083.1:c.342G>A	XP_011540385.1:p.Met114Ile
XM_011542084.1:c.342G>A	XP_011540386.1:p.Met114Ile
XM_011542083.3:c.342G>A	XP_011540385.1:p.Met114Ile
XM_011542084.3:c.342G>A	XP_011540386.1:p.Met114Ile
NM_001215.4:c.330G>A MANE Select	NP_001206.2:p.Met110Ile
NM_001270500.2:c.330G>A	NP_001257429.1:p.Met110Ile
NM_001270501.2:c.150G>A	NP_001257430.1:p.Met50Ile
NM_001270502.2:c.25-1703G>A	NP_001257431.1:n.25-1703G>A