Canonical Allele Identifier: CA439948398

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74283945C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418228C>A , CM000666.2:g.73418228C>A	GRCh38
NC_000004.11:g.74283945C>A , CM000666.1:g.74283945C>A	GRCh37
NC_000004.10:g.74502809C>A	NCBI36
NG_009291.1:g.18974C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1569C>A MANE Select	ENSP00000295897.4:p.Pro523=
ENST00000295897.8:c.1569C>A	ENSP00000295897.4:p.Pro523=
ENST00000401494.7:c.1224C>A	ENSP00000384695.3:p.Pro408=
ENST00000415165.6:c.993C>A	ENSP00000401820.2:p.Pro331=
ENST00000476441.6:c.*848C>A	ENSP00000423727.1:n.*848C>A
ENST00000486939.1:n.223C>A
ENST00000503124.5:c.1119C>A	ENSP00000421027.1:p.Pro373=
ENST00000505649.5:n.1116C>A
ENST00000509063.5:c.1569C>A	ENSP00000422784.1:p.Pro523=
ENST00000511370.1:c.1102C>A
ENST00000621085.4:c.930C>A	ENSP00000483421.1:p.Pro310=
ENST00000621628.4:c.930C>A	ENSP00000480485.1:p.Pro310=
NM_000477.5:c.1569C>A	NP_000468.1:p.Pro523=
NM_000477.6:c.1569C>A	NP_000468.1:p.Pro523=
NM_000477.7:c.1569C>A MANE Select	NP_000468.1:p.Pro523=