Canonical Allele Identifier: CA439800272

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280782T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415065T>A , CM000666.2:g.73415065T>A	GRCh38
NC_000004.11:g.74280782T>A , CM000666.1:g.74280782T>A	GRCh37
NC_000004.10:g.74499646T>A	NCBI36
NG_009291.1:g.15811T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1089T>A MANE Select	ENSP00000295897.4:p.Pro363=
ENST00000295897.8:c.1089T>A	ENSP00000295897.4:p.Pro363=
ENST00000401494.7:c.744T>A	ENSP00000384695.3:p.Pro248=
ENST00000415165.6:c.513T>A	ENSP00000401820.2:p.Pro171=
ENST00000476441.6:c.*368T>A	ENSP00000423727.1:n.*368T>A
ENST00000484992.1:n.409T>A
ENST00000503124.5:c.639T>A	ENSP00000421027.1:p.Pro213=
ENST00000504043.1:n.92T>A
ENST00000505649.5:n.775T>A
ENST00000509063.5:c.1089T>A	ENSP00000422784.1:p.Pro363=
ENST00000511370.1:c.622T>A
ENST00000621085.4:c.491-41T>A	ENSP00000483421.1:n.491-41T>A
ENST00000621628.4:c.487-37T>A	ENSP00000480485.1:n.487-37T>A
NM_000477.5:c.1089T>A	NP_000468.1:p.Pro363=
NM_000477.6:c.1089T>A	NP_000468.1:p.Pro363=
NM_000477.7:c.1089T>A MANE Select	NP_000468.1:p.Pro363=