Canonical Allele Identifier: CA338184917

Gene: CA6

Linked Data

• dbSNP Id: rs1187713209
• gnomAD v4: 1-8957274-C-T
• MyVariant Identifiers: chr1:g.9017333C>T (hg19) ; chr1:g.8957274C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8957274C>T , CM000663.2:g.8957274C>T	GRCh38
NC_000001.10:g.9017333C>T , CM000663.1:g.9017333C>T	GRCh37
NC_000001.9:g.8939920C>T	NCBI36
NG_033975.1:g.16441C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377443.7:c.397C>T MANE Select	ENSP00000366662.2:p.His133Tyr
ENST00000377436.6:c.397C>T	ENSP00000366654.3:p.His133Tyr
ENST00000377442.3:c.217C>T	ENSP00000366661.2:p.His73Tyr
ENST00000377443.6:c.397C>T	ENSP00000366662.2:p.His133Tyr
ENST00000476083.1:n.99-1636C>T
ENST00000549778.5:c.301C>T	ENSP00000447108.1:p.His101Tyr
NM_001215.3:c.397C>T	NP_001206.2:p.His133Tyr
NM_001270500.1:c.397C>T	NP_001257429.1:p.His133Tyr
NM_001270501.1:c.217C>T	NP_001257430.1:p.His73Tyr
NM_001270502.1:c.25-1636C>T	NP_001257431.1:n.25-1636C>T
XM_011542083.1:c.409C>T	XP_011540385.1:p.His137Tyr
XM_011542084.1:c.409C>T	XP_011540386.1:p.His137Tyr
XM_011542083.3:c.409C>T	XP_011540385.1:p.His137Tyr
XM_011542084.3:c.409C>T	XP_011540386.1:p.His137Tyr
NM_001215.4:c.397C>T MANE Select	NP_001206.2:p.His133Tyr
NM_001270500.2:c.397C>T	NP_001257429.1:p.His133Tyr
NM_001270501.2:c.217C>T	NP_001257430.1:p.His73Tyr
NM_001270502.2:c.25-1636C>T	NP_001257431.1:n.25-1636C>T