Canonical Allele Identifier: CA357247233

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74286002C>A (hg19) ; chr4:g.73420285C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420285C>A , CM000666.2:g.73420285C>A	GRCh38
NC_000004.11:g.74286002C>A , CM000666.1:g.74286002C>A	GRCh37
NC_000004.10:g.74504866C>A	NCBI36
NG_009291.1:g.21031C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1817C>A MANE Select	ENSP00000295897.4:p.Ala606Asp
ENST00000295897.8:c.1817C>A	ENSP00000295897.4:p.Ala606Asp
ENST00000401494.7:c.1472C>A	ENSP00000384695.3:p.Ala491Asp
ENST00000415165.6:c.1241C>A	ENSP00000401820.2:p.Ala414Asp
ENST00000476441.6:c.*1096C>A	ENSP00000423727.1:n.*1096C>A
ENST00000495173.1:n.125C>A
ENST00000503124.5:c.1367C>A	ENSP00000421027.1:p.Ala456Asp
ENST00000505649.5:n.1364C>A
ENST00000508932.5:n.207C>A
ENST00000509063.5:c.1785+646C>A	ENSP00000422784.1:n.1785+646C>A
ENST00000511370.1:c.1350C>A
ENST00000621085.4:c.1178C>A	ENSP00000483421.1:p.Ala393Asp
ENST00000621628.4:c.1178C>A	ENSP00000480485.1:p.Ala393Asp
NM_000477.5:c.1817C>A	NP_000468.1:p.Ala606Asp
NM_000477.6:c.1817C>A	NP_000468.1:p.Ala606Asp
NM_000477.7:c.1817C>A MANE Select	NP_000468.1:p.Ala606Asp