Canonical Allele Identifier: CA496904650

Gene: CA5A

Linked Data

• MyVariant Identifiers: chr16:g.87936112G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87902506G>A , CM000678.2:g.87902506G>A	GRCh38
NC_000016.9:g.87936112G>A , CM000678.1:g.87936112G>A	GRCh37
NC_000016.8:g.86493613G>A	NCBI36
NG_033227.1:g.39001C>T
NG_033227.2:g.39024C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648022.1:c.474C>T	ENSP00000497934.1:p.His158=
ENST00000648177.1:c.355C>T	ENSP00000497626.1:p.Leu119=
ENST00000649158.1:c.474C>T	ENSP00000496993.1:p.His158=
ENST00000649794.3:c.474C>T MANE Select	ENSP00000498065.2:p.His158=
ENST00000309893.3:c.474C>T	ENSP00000309649.2:p.His158=
NM_001739.1:c.474C>T	NP_001730.1:p.His158=
XM_011523309.1:c.474C>T	XP_011521611.1:p.His158=
XM_011523310.1:c.474C>T	XP_011521612.1:p.His158=
XR_933417.1:n.593C>T
NM_001739.2:c.474C>T MANE Select	NP_001730.1:p.His158=
XM_011523309.2:c.474C>T	XP_011521611.1:p.His158=
XM_017023646.1:c.474C>T	XP_016879135.1:p.His158=
XM_024450434.1:c.96C>T	XP_024306202.1:p.His32=
XR_002957839.1:n.599C>T
NM_001367225.1:c.474C>T	NP_001354154.1:p.His158=
NR_159798.1:n.553C>T
NR_159799.1:n.434C>T