Canonical Allele Identifier: CA2240759386

Gene: CA5A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902815G= , CM000678.2:g.87902815G=	GRCh38
NC_000016.9:g.87936421G= , CM000678.1:g.87936421G=	GRCh37
NC_000016.8:g.86493922G=	NCBI36
NG_033227.1:g.38692C=
NG_033227.2:g.38715C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.460-295C=	ENSP00000497934.1:n.460-295C=
ENST00000648177.1:c.341-295C=	ENSP00000497626.1:n.341-295C=
ENST00000649158.1:c.460-295C=	ENSP00000496993.1:n.460-295C=
ENST00000649794.3:c.460-295C= MANE Select	ENSP00000498065.2:n.460-295C=
ENST00000309893.3:c.460-295C=	ENSP00000309649.2:n.460-295C=
NM_001739.1:c.460-295C=	NP_001730.1:n.460-295C=
XM_011523309.1:c.460-295C=	XP_011521611.1:n.460-295C=
XM_011523310.1:c.460-295C=	XP_011521612.1:n.460-295C=
XR_933417.1:n.579-295C=
NM_001739.2:c.460-295C= MANE Select	NP_001730.1:n.460-295C=
XM_011523309.2:c.460-295C=	XP_011521611.1:n.460-295C=
XM_017023646.1:c.460-295C=	XP_016879135.1:n.460-295C=
XM_024450434.1:c.82-295C=	XP_024306202.1:n.82-295C=
XR_002957839.1:n.585-295C=
NM_001367225.1:c.460-295C=	NP_001354154.1:n.460-295C=
NR_159798.1:n.539-295C=
NR_159799.1:n.420-295C=