Canonical Allele Identifier: CA357246726

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285349C>A (hg19) ; chr4:g.73419632C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419632C>A , CM000666.2:g.73419632C>A	GRCh38
NC_000004.11:g.74285349C>A , CM000666.1:g.74285349C>A	GRCh37
NC_000004.10:g.74504213C>A	NCBI36
NG_009291.1:g.20378C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1778C>A MANE Select	ENSP00000295897.4:p.Ala593Asp
ENST00000295897.8:c.1778C>A	ENSP00000295897.4:p.Ala593Asp
ENST00000401494.7:c.1433C>A	ENSP00000384695.3:p.Ala478Asp
ENST00000415165.6:c.1202C>A	ENSP00000401820.2:p.Ala401Asp
ENST00000476441.6:c.*1057C>A	ENSP00000423727.1:n.*1057C>A
ENST00000495173.1:n.86C>A
ENST00000503124.5:c.1328C>A	ENSP00000421027.1:p.Ala443Asp
ENST00000505649.5:n.1325C>A
ENST00000508932.5:n.175+177C>A
ENST00000509063.5:c.1778C>A	ENSP00000422784.1:p.Ala593Asp
ENST00000511370.1:c.1311C>A
ENST00000621085.4:c.1139C>A	ENSP00000483421.1:p.Ala380Asp
ENST00000621628.4:c.1139C>A	ENSP00000480485.1:p.Ala380Asp
NM_000477.5:c.1778C>A	NP_000468.1:p.Ala593Asp
NM_000477.6:c.1778C>A	NP_000468.1:p.Ala593Asp
NM_000477.7:c.1778C>A MANE Select	NP_000468.1:p.Ala593Asp