Canonical Allele Identifier: CA1468152709

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409444A= , CM000666.2:g.73409444A=	GRCh38
NC_000004.11:g.74275161A= , CM000666.1:g.74275161A=	GRCh37
NC_000004.10:g.74494025A=	NCBI36
NG_009291.1:g.10190A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.572A= MANE Select	ENSP00000295897.4:p.Glu191=
ENST00000295897.8:c.572A=	ENSP00000295897.4:p.Glu191=
ENST00000401494.7:c.227A=	ENSP00000384695.3:p.Glu76=
ENST00000415165.6:c.138-2552A=	ENSP00000401820.2:n.138-2552A=
ENST00000441319.5:c.578A=	ENSP00000392541.1:p.Glu193=
ENST00000476441.6:c.169A=	ENSP00000423727.1:p.Asn57=
ENST00000503124.5:c.122A=	ENSP00000421027.1:p.Glu41=
ENST00000505649.5:n.258A=
ENST00000509063.5:c.572A=	ENSP00000422784.1:p.Glu191=
ENST00000511370.1:c.105A=
ENST00000514786.1:n.541A=
ENST00000621085.4:c.490+82A=	ENSP00000483421.1:n.490+82A=
ENST00000621628.4:c.486+368A=	ENSP00000480485.1:n.486+368A=
NM_000477.5:c.572A=	NP_000468.1:p.Glu191=
NM_000477.6:c.572A=	NP_000468.1:p.Glu191=
NM_000477.7:c.572A= MANE Select	NP_000468.1:p.Glu191=