Canonical Allele Identifier: CA1468143451

Gene: ALB

Genomic Alleles

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

Transcript Alleles

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