Canonical Allele Identifier: CA1144009013

Gene: CA6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8957268A= , CM000663.2:g.8957268A=	GRCh38
NC_000001.10:g.9017327A= , CM000663.1:g.9017327A=	GRCh37
NC_000001.9:g.8939914A=	NCBI36
NG_033975.1:g.16435A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377443.7:c.391A= MANE Select	ENSP00000366662.2:p.Ile131=
ENST00000377436.6:c.391A=	ENSP00000366654.3:p.Ile131=
ENST00000377442.3:c.211A=	ENSP00000366661.2:p.Ile71=
ENST00000377443.6:c.391A=	ENSP00000366662.2:p.Ile131=
ENST00000476083.1:n.99-1642A=
ENST00000549778.5:c.295A=	ENSP00000447108.1:p.Ile99=
NM_001215.3:c.391A=	NP_001206.2:p.Ile131=
NM_001270500.1:c.391A=	NP_001257429.1:p.Ile131=
NM_001270501.1:c.211A=	NP_001257430.1:p.Ile71=
NM_001270502.1:c.25-1642A=	NP_001257431.1:n.25-1642A=
XM_011542083.1:c.403A=	XP_011540385.1:p.Ile135=
XM_011542084.1:c.403A=	XP_011540386.1:p.Ile135=
XM_011542083.3:c.403A=	XP_011540385.1:p.Ile135=
XM_011542084.3:c.403A=	XP_011540386.1:p.Ile135=
NM_001215.4:c.391A= MANE Select	NP_001206.2:p.Ile131=
NM_001270500.2:c.391A=	NP_001257429.1:p.Ile131=
NM_001270501.2:c.211A=	NP_001257430.1:p.Ile71=
NM_001270502.2:c.25-1642A=	NP_001257431.1:n.25-1642A=