Canonical Allele Identifier: CA357247213

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285998G>A (hg19) ; chr4:g.73420281G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420281G>A , CM000666.2:g.73420281G>A	GRCh38
NC_000004.11:g.74285998G>A , CM000666.1:g.74285998G>A	GRCh37
NC_000004.10:g.74504862G>A	NCBI36
NG_009291.1:g.21027G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1813G>A MANE Select	ENSP00000295897.4:p.Ala605Thr
ENST00000295897.8:c.1813G>A	ENSP00000295897.4:p.Ala605Thr
ENST00000401494.7:c.1468G>A	ENSP00000384695.3:p.Ala490Thr
ENST00000415165.6:c.1237G>A	ENSP00000401820.2:p.Ala413Thr
ENST00000476441.6:c.*1092G>A	ENSP00000423727.1:n.*1092G>A
ENST00000495173.1:n.121G>A
ENST00000503124.5:c.1363G>A	ENSP00000421027.1:p.Ala455Thr
ENST00000505649.5:n.1360G>A
ENST00000508932.5:n.203G>A
ENST00000509063.5:c.1785+642G>A	ENSP00000422784.1:n.1785+642G>A
ENST00000511370.1:c.1346G>A
ENST00000621085.4:c.1174G>A	ENSP00000483421.1:p.Ala392Thr
ENST00000621628.4:c.1174G>A	ENSP00000480485.1:p.Ala392Thr
NM_000477.5:c.1813G>A	NP_000468.1:p.Ala605Thr
NM_000477.6:c.1813G>A	NP_000468.1:p.Ala605Thr
NM_000477.7:c.1813G>A MANE Select	NP_000468.1:p.Ala605Thr