Canonical Allele Identifier: CA1152580379

Gene: CA6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8956948A= , CM000663.2:g.8956948A=	GRCh38
NC_000001.10:g.9017007A= , CM000663.1:g.9017007A=	GRCh37
NC_000001.9:g.8939594A=	NCBI36
NG_033975.1:g.16115A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377443.7:c.260-189A= MANE Select	ENSP00000366662.2:n.260-189A=
ENST00000377436.6:c.260-189A=	ENSP00000366654.3:n.260-189A=
ENST00000377442.3:c.80-189A=	ENSP00000366661.2:n.80-189A=
ENST00000377443.6:c.260-189A=	ENSP00000366662.2:n.260-189A=
ENST00000476083.1:n.99-1962A=
ENST00000549778.5:c.169-194A=	ENSP00000447108.1:n.169-194A=
NM_001215.3:c.260-189A=	NP_001206.2:n.260-189A=
NM_001270500.1:c.260-189A=	NP_001257429.1:n.260-189A=
NM_001270501.1:c.80-189A=	NP_001257430.1:n.80-189A=
NM_001270502.1:c.25-1962A=	NP_001257431.1:n.25-1962A=
XM_011542083.1:c.272-189A=	XP_011540385.1:n.272-189A=
XM_011542084.1:c.272-189A=	XP_011540386.1:n.272-189A=
XM_011542083.3:c.272-189A=	XP_011540385.1:n.272-189A=
XM_011542084.3:c.272-189A=	XP_011540386.1:n.272-189A=
NM_001215.4:c.260-189A= MANE Select	NP_001206.2:n.260-189A=
NM_001270500.2:c.260-189A=	NP_001257429.1:n.260-189A=
NM_001270501.2:c.80-189A=	NP_001257430.1:n.80-189A=
NM_001270502.2:c.25-1962A=	NP_001257431.1:n.25-1962A=