Canonical Allele Identifier: CA2240759173

Gene: CA5A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902445C= , CM000678.2:g.87902445C=	GRCh38
NC_000016.9:g.87936051C= , CM000678.1:g.87936051C=	GRCh37
NC_000016.8:g.86493552C=	NCBI36
NG_033227.1:g.39062G=
NG_033227.2:g.39085G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.535G=	ENSP00000497934.1:p.Val179=
ENST00000648177.1:c.416G=	ENSP00000497626.1:p.Cys139=
ENST00000649158.1:c.535G=	ENSP00000496993.1:p.Val179=
ENST00000649794.3:c.535G= MANE Select	ENSP00000498065.2:p.Val179=
ENST00000309893.3:c.535G=	ENSP00000309649.2:p.Val179=
NM_001739.1:c.535G=	NP_001730.1:p.Val179=
XM_011523309.1:c.535G=	XP_011521611.1:p.Val179=
XM_011523310.1:c.535G=	XP_011521612.1:p.Val179=
XR_933417.1:n.654G=
NM_001739.2:c.535G= MANE Select	NP_001730.1:p.Val179=
XM_011523309.2:c.535G=	XP_011521611.1:p.Val179=
XM_017023646.1:c.535G=	XP_016879135.1:p.Val179=
XM_024450434.1:c.157G=	XP_024306202.1:p.Val53=
XR_002957839.1:n.660G=
NM_001367225.1:c.535G=	NP_001354154.1:p.Val179=
NR_159798.1:n.614G=
NR_159799.1:n.495G=