Canonical Allele Identifier: CA1152580456

Gene: CA6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8956998T= , CM000663.2:g.8956998T=	GRCh38
NC_000001.10:g.9017057T= , CM000663.1:g.9017057T=	GRCh37
NC_000001.9:g.8939644T=	NCBI36
NG_033975.1:g.16165T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377443.7:c.260-139T= MANE Select	ENSP00000366662.2:n.260-139T=
ENST00000377436.6:c.260-139T=	ENSP00000366654.3:n.260-139T=
ENST00000377442.3:c.80-139T=	ENSP00000366661.2:n.80-139T=
ENST00000377443.6:c.260-139T=	ENSP00000366662.2:n.260-139T=
ENST00000476083.1:n.99-1912T=
ENST00000549778.5:c.169-144T=	ENSP00000447108.1:n.169-144T=
NM_001215.3:c.260-139T=	NP_001206.2:n.260-139T=
NM_001270500.1:c.260-139T=	NP_001257429.1:n.260-139T=
NM_001270501.1:c.80-139T=	NP_001257430.1:n.80-139T=
NM_001270502.1:c.25-1912T=	NP_001257431.1:n.25-1912T=
XM_011542083.1:c.272-139T=	XP_011540385.1:n.272-139T=
XM_011542084.1:c.272-139T=	XP_011540386.1:n.272-139T=
XM_011542083.3:c.272-139T=	XP_011540385.1:n.272-139T=
XM_011542084.3:c.272-139T=	XP_011540386.1:n.272-139T=
NM_001215.4:c.260-139T= MANE Select	NP_001206.2:n.260-139T=
NM_001270500.2:c.260-139T=	NP_001257429.1:n.260-139T=
NM_001270501.2:c.80-139T=	NP_001257430.1:n.80-139T=
NM_001270502.2:c.25-1912T=	NP_001257431.1:n.25-1912T=