Canonical Allele Identifier: CA1468152330

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408648G= , CM000666.2:g.73408648G=	GRCh38
NC_000004.11:g.74274365G= , CM000666.1:g.74274365G=	GRCh37
NC_000004.10:g.74493229G=	NCBI36
NG_009291.1:g.9394G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.325G= MANE Select	ENSP00000295897.4:p.Gly109=
ENST00000295897.8:c.325G=	ENSP00000295897.4:p.Gly109=
ENST00000401494.7:c.138-707G=	ENSP00000384695.3:n.138-707G=
ENST00000415165.6:c.138-3348G=	ENSP00000401820.2:n.138-3348G=
ENST00000441319.5:c.331G=	ENSP00000392541.1:p.Gly111=
ENST00000476441.6:c.80-707G=	ENSP00000423727.1:n.80-707G=
ENST00000503124.5:c.33-707G=	ENSP00000421027.1:n.33-707G=
ENST00000505649.5:n.11G=
ENST00000509063.5:c.325G=	ENSP00000422784.1:p.Gly109=
ENST00000510166.5:n.361G=
ENST00000514786.1:n.294G=
ENST00000515133.5:n.366G=
ENST00000621085.4:c.325G=	ENSP00000483421.1:p.Gly109=
ENST00000621628.4:c.325G=	ENSP00000480485.1:p.Gly109=
NM_000477.5:c.325G=	NP_000468.1:p.Gly109=
NM_000477.6:c.325G=	NP_000468.1:p.Gly109=
NM_000477.7:c.325G= MANE Select	NP_000468.1:p.Gly109=