Canonical Allele Identifier: CA1468150507

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406266A= , CM000666.2:g.73406266A=	GRCh38
NC_000004.11:g.74271983A= , CM000666.1:g.74271983A=	GRCh37
NC_000004.10:g.74490847A=	NCBI36
NG_009291.1:g.7012A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.138-363A= MANE Select	ENSP00000295897.4:n.138-363A=
ENST00000295897.8:c.138-363A=	ENSP00000295897.4:n.138-363A=
ENST00000401494.7:c.137+1093A=	ENSP00000384695.3:n.137+1093A=
ENST00000415165.6:c.137+1093A=	ENSP00000401820.2:n.137+1093A=
ENST00000441319.5:c.144-363A=	ENSP00000392541.1:n.144-363A=
ENST00000476441.6:c.79+1860A=	ENSP00000423727.1:n.79+1860A=
ENST00000503124.5:c.-101-363A=	ENSP00000421027.1:n.-101-363A=
ENST00000509063.5:c.138-363A=	ENSP00000422784.1:n.138-363A=
ENST00000510166.5:n.174-363A=
ENST00000514786.1:n.107-363A=
ENST00000515133.5:n.179-363A=
ENST00000621085.4:c.138-363A=	ENSP00000483421.1:n.138-363A=
ENST00000621628.4:c.138-363A=	ENSP00000480485.1:n.138-363A=
NM_000477.5:c.138-363A=	NP_000468.1:n.138-363A=
NM_000477.6:c.138-363A=	NP_000468.1:n.138-363A=
NM_000477.7:c.138-363A= MANE Select	NP_000468.1:n.138-363A=