Canonical Allele Identifier: CA338184688

Gene: CA6

Linked Data

• gnomAD v3: 1-8957168-G-T
• gnomAD v4: 1-8957168-G-T
• MyVariant Identifiers: chr1:g.9017227G>T (hg19) ; chr1:g.8957168G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8957168G>T , CM000663.2:g.8957168G>T	GRCh38
NC_000001.10:g.9017227G>T , CM000663.1:g.9017227G>T	GRCh37
NC_000001.9:g.8939814G>T	NCBI36
NG_033975.1:g.16335G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377443.7:c.291G>T MANE Select	ENSP00000366662.2:p.Met97Ile
ENST00000377436.6:c.291G>T	ENSP00000366654.3:p.Met97Ile
ENST00000377442.3:c.111G>T	ENSP00000366661.2:p.Met37Ile
ENST00000377443.6:c.291G>T	ENSP00000366662.2:p.Met97Ile
ENST00000476083.1:n.99-1742G>T
ENST00000549778.5:c.195G>T	ENSP00000447108.1:p.Met65Ile
NM_001215.3:c.291G>T	NP_001206.2:p.Met97Ile
NM_001270500.1:c.291G>T	NP_001257429.1:p.Met97Ile
NM_001270501.1:c.111G>T	NP_001257430.1:p.Met37Ile
NM_001270502.1:c.25-1742G>T	NP_001257431.1:n.25-1742G>T
XM_011542083.1:c.303G>T	XP_011540385.1:p.Met101Ile
XM_011542084.1:c.303G>T	XP_011540386.1:p.Met101Ile
XM_011542083.3:c.303G>T	XP_011540385.1:p.Met101Ile
XM_011542084.3:c.303G>T	XP_011540386.1:p.Met101Ile
NM_001215.4:c.291G>T MANE Select	NP_001206.2:p.Met97Ile
NM_001270500.2:c.291G>T	NP_001257429.1:p.Met97Ile
NM_001270501.2:c.111G>T	NP_001257430.1:p.Met37Ile
NM_001270502.2:c.25-1742G>T	NP_001257431.1:n.25-1742G>T