Canonical Allele Identifier: CA439948391

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74283933A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418216A>G , CM000666.2:g.73418216A>G	GRCh38
NC_000004.11:g.74283933A>G , CM000666.1:g.74283933A>G	GRCh37
NC_000004.10:g.74502797A>G	NCBI36
NG_009291.1:g.18962A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1557A>G MANE Select	ENSP00000295897.4:p.Glu519=
ENST00000295897.8:c.1557A>G	ENSP00000295897.4:p.Glu519=
ENST00000401494.7:c.1212A>G	ENSP00000384695.3:p.Glu404=
ENST00000415165.6:c.981A>G	ENSP00000401820.2:p.Glu327=
ENST00000476441.6:c.*836A>G	ENSP00000423727.1:n.*836A>G
ENST00000486939.1:n.211A>G
ENST00000503124.5:c.1107A>G	ENSP00000421027.1:p.Glu369=
ENST00000505649.5:n.1104A>G
ENST00000509063.5:c.1557A>G	ENSP00000422784.1:p.Glu519=
ENST00000511370.1:c.1090A>G
ENST00000621085.4:c.918A>G	ENSP00000483421.1:p.Glu306=
ENST00000621628.4:c.918A>G	ENSP00000480485.1:p.Glu306=
NM_000477.5:c.1557A>G	NP_000468.1:p.Glu519=
NM_000477.6:c.1557A>G	NP_000468.1:p.Glu519=
NM_000477.7:c.1557A>G MANE Select	NP_000468.1:p.Glu519=