Canonical Allele Identifier: CA1468143516

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415105T= , CM000666.2:g.73415105T=	GRCh38
NC_000004.11:g.74280822T= , CM000666.1:g.74280822T=	GRCh37
NC_000004.10:g.74499686T=	NCBI36
NG_009291.1:g.15851T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1129T= MANE Select	ENSP00000295897.4:p.Tyr377=
ENST00000295897.8:c.1129T=	ENSP00000295897.4:p.Tyr377=
ENST00000401494.7:c.784T=	ENSP00000384695.3:p.Tyr262=
ENST00000415165.6:c.553T=	ENSP00000401820.2:p.Tyr185=
ENST00000476441.6:c.*408T=	ENSP00000423727.1:n.*408T=
ENST00000484992.1:n.449T=
ENST00000503124.5:c.679T=	ENSP00000421027.1:p.Tyr227=
ENST00000504043.1:n.132T=
ENST00000505649.5:n.815T=
ENST00000509063.5:c.1129T=	ENSP00000422784.1:p.Tyr377=
ENST00000511370.1:c.662T=
ENST00000621085.4:c.491-1T=	ENSP00000483421.1:n.491-1T=
ENST00000621628.4:c.490T=	ENSP00000480485.1:p.Tyr164=
NM_000477.5:c.1129T=	NP_000468.1:p.Tyr377=
NM_000477.6:c.1129T=	NP_000468.1:p.Tyr377=
NM_000477.7:c.1129T= MANE Select	NP_000468.1:p.Tyr377=