Canonical Allele Identifier: CA2240759196

Gene: CA5A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902503C= , CM000678.2:g.87902503C=	GRCh38
NC_000016.9:g.87936109C= , CM000678.1:g.87936109C=	GRCh37
NC_000016.8:g.86493610C=	NCBI36
NG_033227.1:g.39004G=
NG_033227.2:g.39027G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.477G=	ENSP00000497934.1:p.Trp159=
ENST00000648177.1:c.358G=	ENSP00000497626.1:p.Glu120=
ENST00000649158.1:c.477G=	ENSP00000496993.1:p.Trp159=
ENST00000649794.3:c.477G= MANE Select	ENSP00000498065.2:p.Trp159=
ENST00000309893.3:c.477G=	ENSP00000309649.2:p.Trp159=
NM_001739.1:c.477G=	NP_001730.1:p.Trp159=
XM_011523309.1:c.477G=	XP_011521611.1:p.Trp159=
XM_011523310.1:c.477G=	XP_011521612.1:p.Trp159=
XR_933417.1:n.596G=
NM_001739.2:c.477G= MANE Select	NP_001730.1:p.Trp159=
XM_011523309.2:c.477G=	XP_011521611.1:p.Trp159=
XM_017023646.1:c.477G=	XP_016879135.1:p.Trp159=
XM_024450434.1:c.99G=	XP_024306202.1:p.Trp33=
XR_002957839.1:n.602G=
NM_001367225.1:c.477G=	NP_001354154.1:p.Trp159=
NR_159798.1:n.556G=
NR_159799.1:n.437G=