Canonical Allele Identifier: CA1468152367

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408743G= , CM000666.2:g.73408743G=	GRCh38
NC_000004.11:g.74274460G= , CM000666.1:g.74274460G=	GRCh37
NC_000004.10:g.74493324G=	NCBI36
NG_009291.1:g.9489G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.420G= MANE Select	ENSP00000295897.4:p.Val140=
ENST00000295897.8:c.420G=	ENSP00000295897.4:p.Val140=
ENST00000401494.7:c.138-612G=	ENSP00000384695.3:n.138-612G=
ENST00000415165.6:c.138-3253G=	ENSP00000401820.2:n.138-3253G=
ENST00000441319.5:c.426G=	ENSP00000392541.1:p.Val142=
ENST00000476441.6:c.80-612G=	ENSP00000423727.1:n.80-612G=
ENST00000503124.5:c.33-612G=	ENSP00000421027.1:n.33-612G=
ENST00000505649.5:n.106G=
ENST00000509063.5:c.420G=	ENSP00000422784.1:p.Val140=
ENST00000510166.5:n.456G=
ENST00000514786.1:n.389G=
ENST00000515133.5:n.461G=
ENST00000621085.4:c.420G=	ENSP00000483421.1:p.Val140=
ENST00000621628.4:c.420G=	ENSP00000480485.1:p.Val140=
NM_000477.5:c.420G=	NP_000468.1:p.Val140=
NM_000477.6:c.420G=	NP_000468.1:p.Val140=
NM_000477.7:c.420G= MANE Select	NP_000468.1:p.Val140=