Canonical Allele Identifier: CA1468140665

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73412027A= , CM000666.2:g.73412027A=	GRCh38
NC_000004.11:g.74277744A= , CM000666.1:g.74277744A=	GRCh37
NC_000004.10:g.74496608A=	NCBI36
NG_009291.1:g.12773A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.745A= MANE Select	ENSP00000295897.4:p.Lys249=
ENST00000295897.8:c.745A=	ENSP00000295897.4:p.Lys249=
ENST00000401494.7:c.400A=	ENSP00000384695.3:p.Lys134=
ENST00000415165.6:c.169A=	ENSP00000401820.2:p.Lys57=
ENST00000476441.6:c.*24A=	ENSP00000423727.1:n.*24A=
ENST00000503124.5:c.295A=	ENSP00000421027.1:p.Lys99=
ENST00000505649.5:n.431A=
ENST00000507673.1:n.62A=
ENST00000509063.5:c.745A=	ENSP00000422784.1:p.Lys249=
ENST00000511370.1:c.278A=
ENST00000621085.4:c.490+2665A=	ENSP00000483421.1:n.490+2665A=
ENST00000621628.4:c.486+2951A=	ENSP00000480485.1:n.486+2951A=
NM_000477.5:c.745A=	NP_000468.1:p.Lys249=
NM_000477.6:c.745A=	NP_000468.1:p.Lys249=
NM_000477.7:c.745A= MANE Select	NP_000468.1:p.Lys249=