Canonical Allele Identifier: CA2240759183

Gene: CA5A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902471G= , CM000678.2:g.87902471G=	GRCh38
NC_000016.9:g.87936077G= , CM000678.1:g.87936077G=	GRCh37
NC_000016.8:g.86493578G=	NCBI36
NG_033227.1:g.39036C=
NG_033227.2:g.39059C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.509C=	ENSP00000497934.1:p.Ala170=
ENST00000648177.1:c.390C=	ENSP00000497626.1:p.Ser130=
ENST00000649158.1:c.509C=	ENSP00000496993.1:p.Ala170=
ENST00000649794.3:c.509C= MANE Select	ENSP00000498065.2:p.Ala170=
ENST00000309893.3:c.509C=	ENSP00000309649.2:p.Ala170=
NM_001739.1:c.509C=	NP_001730.1:p.Ala170=
XM_011523309.1:c.509C=	XP_011521611.1:p.Ala170=
XM_011523310.1:c.509C=	XP_011521612.1:p.Ala170=
XR_933417.1:n.628C=
NM_001739.2:c.509C= MANE Select	NP_001730.1:p.Ala170=
XM_011523309.2:c.509C=	XP_011521611.1:p.Ala170=
XM_017023646.1:c.509C=	XP_016879135.1:p.Ala170=
XM_024450434.1:c.131C=	XP_024306202.1:p.Ala44=
XR_002957839.1:n.634C=
NM_001367225.1:c.509C=	NP_001354154.1:p.Ala170=
NR_159798.1:n.588C=
NR_159799.1:n.469C=