Canonical Allele Identifier: CA1468140616

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73411996G= , CM000666.2:g.73411996G=	GRCh38
NC_000004.11:g.74277713G= , CM000666.1:g.74277713G=	GRCh37
NC_000004.10:g.74496577G=	NCBI36
NG_009291.1:g.12742G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.714G= MANE Select	ENSP00000295897.4:p.Trp238=
ENST00000295897.8:c.714G=	ENSP00000295897.4:p.Trp238=
ENST00000401494.7:c.369G=	ENSP00000384695.3:p.Trp123=
ENST00000415165.6:c.138G=	ENSP00000401820.2:p.Leu46=
ENST00000476441.6:c.311G=	ENSP00000423727.1:p.Gly104=
ENST00000503124.5:c.264G=	ENSP00000421027.1:p.Trp88=
ENST00000505649.5:n.400G=
ENST00000507673.1:n.31G=
ENST00000509063.5:c.714G=	ENSP00000422784.1:p.Trp238=
ENST00000511370.1:c.247G=
ENST00000621085.4:c.490+2634G=	ENSP00000483421.1:n.490+2634G=
ENST00000621628.4:c.486+2920G=	ENSP00000480485.1:n.486+2920G=
NM_000477.5:c.714G=	NP_000468.1:p.Trp238=
NM_000477.6:c.714G=	NP_000468.1:p.Trp238=
NM_000477.7:c.714G= MANE Select	NP_000468.1:p.Trp238=