Canonical Allele Identifier: CA439801066

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285973T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420256T>A , CM000666.2:g.73420256T>A	GRCh38
NC_000004.11:g.74285973T>A , CM000666.1:g.74285973T>A	GRCh37
NC_000004.10:g.74504837T>A	NCBI36
NG_009291.1:g.21002T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1788T>A MANE Select	ENSP00000295897.4:p.Gly596=
ENST00000295897.8:c.1788T>A	ENSP00000295897.4:p.Gly596=
ENST00000401494.7:c.1443T>A	ENSP00000384695.3:p.Gly481=
ENST00000415165.6:c.1212T>A	ENSP00000401820.2:p.Gly404=
ENST00000476441.6:c.*1067T>A	ENSP00000423727.1:n.*1067T>A
ENST00000495173.1:n.96T>A
ENST00000503124.5:c.1338T>A	ENSP00000421027.1:p.Gly446=
ENST00000505649.5:n.1335T>A
ENST00000508932.5:n.178T>A
ENST00000509063.5:c.1785+617T>A	ENSP00000422784.1:n.1785+617T>A
ENST00000511370.1:c.1321T>A
ENST00000621085.4:c.1149T>A	ENSP00000483421.1:p.Gly383=
ENST00000621628.4:c.1149T>A	ENSP00000480485.1:p.Gly383=
NM_000477.5:c.1788T>A	NP_000468.1:p.Gly596=
NM_000477.6:c.1788T>A	NP_000468.1:p.Gly596=
NM_000477.7:c.1788T>A MANE Select	NP_000468.1:p.Gly596=