Canonical Allele Identifier: CA1468143439

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415061A= , CM000666.2:g.73415061A=	GRCh38
NC_000004.11:g.74280778A= , CM000666.1:g.74280778A=	GRCh37
NC_000004.10:g.74499642A=	NCBI36
NG_009291.1:g.15807A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1085A= MANE Select	ENSP00000295897.4:p.His362=
ENST00000295897.8:c.1085A=	ENSP00000295897.4:p.His362=
ENST00000401494.7:c.740A=	ENSP00000384695.3:p.His247=
ENST00000415165.6:c.509A=	ENSP00000401820.2:p.His170=
ENST00000476441.6:c.*364A=	ENSP00000423727.1:n.*364A=
ENST00000484992.1:n.405A=
ENST00000503124.5:c.635A=	ENSP00000421027.1:p.His212=
ENST00000504043.1:n.88A=
ENST00000505649.5:n.771A=
ENST00000509063.5:c.1085A=	ENSP00000422784.1:p.His362=
ENST00000511370.1:c.618A=
ENST00000621085.4:c.491-45A=	ENSP00000483421.1:n.491-45A=
ENST00000621628.4:c.487-41A=	ENSP00000480485.1:n.487-41A=
NM_000477.5:c.1085A=	NP_000468.1:p.His362=
NM_000477.6:c.1085A=	NP_000468.1:p.His362=
NM_000477.7:c.1085A= MANE Select	NP_000468.1:p.His362=