Canonical Allele Identifier: CA1468146853

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418165A= , CM000666.2:g.73418165A=	GRCh38
NC_000004.11:g.74283882A= , CM000666.1:g.74283882A=	GRCh37
NC_000004.10:g.74502746A=	NCBI36
NG_009291.1:g.18911A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1506A= MANE Select	ENSP00000295897.4:p.Thr502=
ENST00000295897.8:c.1506A=	ENSP00000295897.4:p.Thr502=
ENST00000401494.7:c.1161A=	ENSP00000384695.3:p.Thr387=
ENST00000415165.6:c.930A=	ENSP00000401820.2:p.Thr310=
ENST00000476441.6:c.*785A=	ENSP00000423727.1:n.*785A=
ENST00000486939.1:n.160A=
ENST00000503124.5:c.1056A=	ENSP00000421027.1:p.Thr352=
ENST00000505649.5:n.1053A=
ENST00000509063.5:c.1506A=	ENSP00000422784.1:p.Thr502=
ENST00000511370.1:c.1039A=
ENST00000621085.4:c.867A=	ENSP00000483421.1:p.Thr289=
ENST00000621628.4:c.867A=	ENSP00000480485.1:p.Thr289=
NM_000477.5:c.1506A=	NP_000468.1:p.Thr502=
NM_000477.6:c.1506A=	NP_000468.1:p.Thr502=
NM_000477.7:c.1506A= MANE Select	NP_000468.1:p.Thr502=