Canonical Allele Identifier: CA439800951

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285299A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419582A>G , CM000666.2:g.73419582A>G	GRCh38
NC_000004.11:g.74285299A>G , CM000666.1:g.74285299A>G	GRCh37
NC_000004.10:g.74504163A>G	NCBI36
NG_009291.1:g.20328A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1728A>G MANE Select	ENSP00000295897.4:p.Ala576=
ENST00000295897.8:c.1728A>G	ENSP00000295897.4:p.Ala576=
ENST00000401494.7:c.1383A>G	ENSP00000384695.3:p.Ala461=
ENST00000415165.6:c.1152A>G	ENSP00000401820.2:p.Ala384=
ENST00000476441.6:c.*1007A>G	ENSP00000423727.1:n.*1007A>G
ENST00000495173.1:n.36A>G
ENST00000503124.5:c.1278A>G	ENSP00000421027.1:p.Ala426=
ENST00000505649.5:n.1275A>G
ENST00000508932.5:n.175+127A>G
ENST00000509063.5:c.1728A>G	ENSP00000422784.1:p.Ala576=
ENST00000511370.1:c.1261A>G
ENST00000621085.4:c.1089A>G	ENSP00000483421.1:p.Ala363=
ENST00000621628.4:c.1089A>G	ENSP00000480485.1:p.Ala363=
NM_000477.5:c.1728A>G	NP_000468.1:p.Ala576=
NM_000477.6:c.1728A>G	NP_000468.1:p.Ala576=
NM_000477.7:c.1728A>G MANE Select	NP_000468.1:p.Ala576=