Canonical Allele Identifier: CA357246502

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285318T>A (hg19) ; chr4:g.73419601T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419601T>A , CM000666.2:g.73419601T>A	GRCh38
NC_000004.11:g.74285318T>A , CM000666.1:g.74285318T>A	GRCh37
NC_000004.10:g.74504182T>A	NCBI36
NG_009291.1:g.20347T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1747T>A MANE Select	ENSP00000295897.4:p.Cys583Ser
ENST00000295897.8:c.1747T>A	ENSP00000295897.4:p.Cys583Ser
ENST00000401494.7:c.1402T>A	ENSP00000384695.3:p.Cys468Ser
ENST00000415165.6:c.1171T>A	ENSP00000401820.2:p.Cys391Ser
ENST00000476441.6:c.*1026T>A	ENSP00000423727.1:n.*1026T>A
ENST00000495173.1:n.55T>A
ENST00000503124.5:c.1297T>A	ENSP00000421027.1:p.Cys433Ser
ENST00000505649.5:n.1294T>A
ENST00000508932.5:n.175+146T>A
ENST00000509063.5:c.1747T>A	ENSP00000422784.1:p.Cys583Ser
ENST00000511370.1:c.1280T>A
ENST00000621085.4:c.1108T>A	ENSP00000483421.1:p.Cys370Ser
ENST00000621628.4:c.1108T>A	ENSP00000480485.1:p.Cys370Ser
NM_000477.5:c.1747T>A	NP_000468.1:p.Cys583Ser
NM_000477.6:c.1747T>A	NP_000468.1:p.Cys583Ser
NM_000477.7:c.1747T>A MANE Select	NP_000468.1:p.Cys583Ser