Canonical Allele Identifier: CA2240759185

Gene: CA5A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902476C= , CM000678.2:g.87902476C=	GRCh38
NC_000016.9:g.87936082C= , CM000678.1:g.87936082C=	GRCh37
NC_000016.8:g.86493583C=	NCBI36
NG_033227.1:g.39031G=
NG_033227.2:g.39054G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.504G=	ENSP00000497934.1:p.Lys168=
ENST00000648177.1:c.385G=	ENSP00000497626.1:p.Gly129=
ENST00000649158.1:c.504G=	ENSP00000496993.1:p.Lys168=
ENST00000649794.3:c.504G= MANE Select	ENSP00000498065.2:p.Lys168=
ENST00000309893.3:c.504G=	ENSP00000309649.2:p.Lys168=
NM_001739.1:c.504G=	NP_001730.1:p.Lys168=
XM_011523309.1:c.504G=	XP_011521611.1:p.Lys168=
XM_011523310.1:c.504G=	XP_011521612.1:p.Lys168=
XR_933417.1:n.623G=
NM_001739.2:c.504G= MANE Select	NP_001730.1:p.Lys168=
XM_011523309.2:c.504G=	XP_011521611.1:p.Lys168=
XM_017023646.1:c.504G=	XP_016879135.1:p.Lys168=
XM_024450434.1:c.126G=	XP_024306202.1:p.Lys42=
XR_002957839.1:n.629G=
NM_001367225.1:c.504G=	NP_001354154.1:p.Lys168=
NR_159798.1:n.583G=
NR_159799.1:n.464G=