Canonical Allele Identifier: CA1468141969

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413456T= , CM000666.2:g.73413456T=	GRCh38
NC_000004.11:g.74279173T= , CM000666.1:g.74279173T=	GRCh37
NC_000004.10:g.74498037T=	NCBI36
NG_009291.1:g.14202T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.880T= MANE Select	ENSP00000295897.4:p.Ser294=
ENST00000295897.8:c.880T=	ENSP00000295897.4:p.Ser294=
ENST00000401494.7:c.535T=	ENSP00000384695.3:p.Ser179=
ENST00000415165.6:c.304T=	ENSP00000401820.2:p.Ser102=
ENST00000476441.6:c.*159T=	ENSP00000423727.1:n.*159T=
ENST00000484992.1:n.200T=
ENST00000503124.5:c.430T=	ENSP00000421027.1:p.Ser144=
ENST00000505649.5:n.566T=
ENST00000509063.5:c.880T=	ENSP00000422784.1:p.Ser294=
ENST00000511370.1:c.413T=
ENST00000621085.4:c.491-1650T=	ENSP00000483421.1:n.491-1650T=
ENST00000621628.4:c.487-1646T=	ENSP00000480485.1:n.487-1646T=
NM_000477.5:c.880T=	NP_000468.1:p.Ser294=
NM_000477.6:c.880T=	NP_000468.1:p.Ser294=
NM_000477.7:c.880T= MANE Select	NP_000468.1:p.Ser294=