Canonical Allele Identifier: CA1468146788

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418129A= , CM000666.2:g.73418129A=	GRCh38
NC_000004.11:g.74283846A= , CM000666.1:g.74283846A=	GRCh37
NC_000004.10:g.74502710A=	NCBI36
NG_009291.1:g.18875A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1470A= MANE Select	ENSP00000295897.4:p.Lys490=
ENST00000295897.8:c.1470A=	ENSP00000295897.4:p.Lys490=
ENST00000401494.7:c.1125A=	ENSP00000384695.3:p.Lys375=
ENST00000415165.6:c.894A=	ENSP00000401820.2:p.Lys298=
ENST00000476441.6:c.*749A=	ENSP00000423727.1:n.*749A=
ENST00000486939.1:n.124A=
ENST00000503124.5:c.1020A=	ENSP00000421027.1:p.Lys340=
ENST00000505649.5:n.1017A=
ENST00000509063.5:c.1470A=	ENSP00000422784.1:p.Lys490=
ENST00000511370.1:c.1003A=
ENST00000621085.4:c.831A=	ENSP00000483421.1:p.Lys277=
ENST00000621628.4:c.831A=	ENSP00000480485.1:p.Lys277=
NM_000477.5:c.1470A=	NP_000468.1:p.Lys490=
NM_000477.6:c.1470A=	NP_000468.1:p.Lys490=
NM_000477.7:c.1470A= MANE Select	NP_000468.1:p.Lys490=