Canonical Allele Identifier: CA1468140725

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73412072A= , CM000666.2:g.73412072A=	GRCh38
NC_000004.11:g.74277789A= , CM000666.1:g.74277789A=	GRCh37
NC_000004.10:g.74496653A=	NCBI36
NG_009291.1:g.12818A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.790A= MANE Select	ENSP00000295897.4:p.Lys264=
ENST00000295897.8:c.790A=	ENSP00000295897.4:p.Lys264=
ENST00000401494.7:c.445A=	ENSP00000384695.3:p.Lys149=
ENST00000415165.6:c.214A=	ENSP00000401820.2:p.Lys72=
ENST00000476441.6:c.*69A=	ENSP00000423727.1:n.*69A=
ENST00000503124.5:c.340A=	ENSP00000421027.1:p.Lys114=
ENST00000505649.5:n.476A=
ENST00000507673.1:n.107A=
ENST00000509063.5:c.790A=	ENSP00000422784.1:p.Lys264=
ENST00000511370.1:c.323A=
ENST00000621085.4:c.490+2710A=	ENSP00000483421.1:n.490+2710A=
ENST00000621628.4:c.486+2996A=	ENSP00000480485.1:n.486+2996A=
NM_000477.5:c.790A=	NP_000468.1:p.Lys264=
NM_000477.6:c.790A=	NP_000468.1:p.Lys264=
NM_000477.7:c.790A= MANE Select	NP_000468.1:p.Lys264=