Canonical Allele Identifier: CA1468148225

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419575A= , CM000666.2:g.73419575A=	GRCh38
NC_000004.11:g.74285292A= , CM000666.1:g.74285292A=	GRCh37
NC_000004.10:g.74504156A=	NCBI36
NG_009291.1:g.20321A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000477.7:c.1721A= MANE Select	NP_000468.1:p.Asp574=
ENST00000295897.9:c.1721A= MANE Select	ENSP00000295897.4:p.Asp574=
NM_000477.5:c.1721A=	NP_000468.1:p.Asp574=
NM_000477.6:c.1721A=	NP_000468.1:p.Asp574=
ENST00000295897.8:c.1721A=	ENSP00000295897.4:p.Asp574=
ENST00000401494.7:c.1376A=	ENSP00000384695.3:p.Asp459=
ENST00000415165.6:c.1145A=	ENSP00000401820.2:p.Asp382=
ENST00000476441.6:c.*1000A=	ENSP00000423727.1:n.*1000A=
ENST00000495173.1:n.29A=
ENST00000503124.5:c.1271A=	ENSP00000421027.1:p.Asp424=
ENST00000505649.5:n.1268A=
ENST00000508932.5:n.175+120A=
ENST00000509063.5:c.1721A=	ENSP00000422784.1:p.Asp574=
ENST00000511370.1:c.1254A=
ENST00000621085.4:c.1082A=	ENSP00000483421.1:p.Asp361=
ENST00000621628.4:c.1082A=	ENSP00000480485.1:p.Asp361=