Canonical Allele Identifier: CA1468152724

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409484A= , CM000666.2:g.73409484A=	GRCh38
NC_000004.11:g.74275201A= , CM000666.1:g.74275201A=	GRCh37
NC_000004.10:g.74494065A=	NCBI36
NG_009291.1:g.10230A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.612A= MANE Select	ENSP00000295897.4:p.Pro204=
ENST00000295897.8:c.612A=	ENSP00000295897.4:p.Pro204=
ENST00000401494.7:c.267A=	ENSP00000384695.3:p.Pro89=
ENST00000415165.6:c.138-2512A=	ENSP00000401820.2:n.138-2512A=
ENST00000476441.6:c.209A=	ENSP00000423727.1:p.Gln70=
ENST00000503124.5:c.162A=	ENSP00000421027.1:p.Pro54=
ENST00000505649.5:n.298A=
ENST00000509063.5:c.612A=	ENSP00000422784.1:p.Pro204=
ENST00000511370.1:c.145A=
ENST00000621085.4:c.490+122A=	ENSP00000483421.1:n.490+122A=
ENST00000621628.4:c.486+408A=	ENSP00000480485.1:n.486+408A=
NM_000477.5:c.612A=	NP_000468.1:p.Pro204=
NM_000477.6:c.612A=	NP_000468.1:p.Pro204=
NM_000477.7:c.612A= MANE Select	NP_000468.1:p.Pro204=