Canonical Allele Identifier: CA357247287

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74286008G>A (hg19) ; chr4:g.73420291G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420291G>A , CM000666.2:g.73420291G>A	GRCh38
NC_000004.11:g.74286008G>A , CM000666.1:g.74286008G>A	GRCh37
NC_000004.10:g.74504872G>A	NCBI36
NG_009291.1:g.21037G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1823G>A MANE Select	ENSP00000295897.4:p.Gly608Asp
ENST00000295897.8:c.1823G>A	ENSP00000295897.4:p.Gly608Asp
ENST00000401494.7:c.1478G>A	ENSP00000384695.3:p.Gly493Asp
ENST00000415165.6:c.1247G>A	ENSP00000401820.2:p.Gly416Asp
ENST00000476441.6:c.*1102G>A	ENSP00000423727.1:n.*1102G>A
ENST00000495173.1:n.131G>A
ENST00000503124.5:c.1373G>A	ENSP00000421027.1:p.Gly458Asp
ENST00000505649.5:n.1370G>A
ENST00000508932.5:n.213G>A
ENST00000509063.5:c.1785+652G>A	ENSP00000422784.1:n.1785+652G>A
ENST00000511370.1:c.1356G>A
ENST00000621085.4:c.1184G>A	ENSP00000483421.1:p.Gly395Asp
ENST00000621628.4:c.1184G>A	ENSP00000480485.1:p.Gly395Asp
NM_000477.5:c.1823G>A	NP_000468.1:p.Gly608Asp
NM_000477.6:c.1823G>A	NP_000468.1:p.Gly608Asp
NM_000477.7:c.1823G>A MANE Select	NP_000468.1:p.Gly608Asp