Canonical Allele Identifier: CA439800889

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285260A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419543A>T , CM000666.2:g.73419543A>T	GRCh38
NC_000004.11:g.74285260A>T , CM000666.1:g.74285260A>T	GRCh37
NC_000004.10:g.74504124A>T	NCBI36
NG_009291.1:g.20289A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1689A>T MANE Select	ENSP00000295897.4:p.Ala563=
ENST00000295897.8:c.1689A>T	ENSP00000295897.4:p.Ala563=
ENST00000401494.7:c.1344A>T	ENSP00000384695.3:p.Ala448=
ENST00000415165.6:c.1113A>T	ENSP00000401820.2:p.Ala371=
ENST00000476441.6:c.*968A>T	ENSP00000423727.1:n.*968A>T
ENST00000486939.1:n.343A>T
ENST00000503124.5:c.1239A>T	ENSP00000421027.1:p.Ala413=
ENST00000505649.5:n.1236A>T
ENST00000508932.5:n.175+88A>T
ENST00000509063.5:c.1689A>T	ENSP00000422784.1:p.Ala563=
ENST00000511370.1:c.1222A>T
ENST00000621085.4:c.1050A>T	ENSP00000483421.1:p.Ala350=
ENST00000621628.4:c.1050A>T	ENSP00000480485.1:p.Ala350=
NM_000477.5:c.1689A>T	NP_000468.1:p.Ala563=
NM_000477.6:c.1689A>T	NP_000468.1:p.Ala563=
NM_000477.7:c.1689A>T MANE Select	NP_000468.1:p.Ala563=