Canonical Allele Identifier: CA1468151356

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73407160T= , CM000666.2:g.73407160T=	GRCh38
NC_000004.11:g.74272877T= , CM000666.1:g.74272877T=	GRCh37
NC_000004.10:g.74491741T=	NCBI36
NG_009291.1:g.7906T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.270+399T= MANE Select	ENSP00000295897.4:n.270+399T=
ENST00000295897.8:c.270+399T=	ENSP00000295897.4:n.270+399T=
ENST00000401494.7:c.137+1987T=	ENSP00000384695.3:n.137+1987T=
ENST00000415165.6:c.137+1987T=	ENSP00000401820.2:n.137+1987T=
ENST00000441319.5:c.276+399T=	ENSP00000392541.1:n.276+399T=
ENST00000476441.6:c.80-2195T=	ENSP00000423727.1:n.80-2195T=
ENST00000503124.5:c.32+399T=	ENSP00000421027.1:n.32+399T=
ENST00000509063.5:c.270+399T=	ENSP00000422784.1:n.270+399T=
ENST00000510166.5:n.306+399T=
ENST00000514786.1:n.239+399T=
ENST00000515133.5:n.311+399T=
ENST00000621085.4:c.270+399T=	ENSP00000483421.1:n.270+399T=
ENST00000621628.4:c.270+399T=	ENSP00000480485.1:n.270+399T=
NM_000477.5:c.270+399T=	NP_000468.1:n.270+399T=
NM_000477.6:c.270+399T=	NP_000468.1:n.270+399T=
NM_000477.7:c.270+399T= MANE Select	NP_000468.1:n.270+399T=