Canonical Allele Identifier: CA1468146759

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418107A= , CM000666.2:g.73418107A=	GRCh38
NC_000004.11:g.74283824A= , CM000666.1:g.74283824A=	GRCh37
NC_000004.10:g.74502688A=	NCBI36
NG_009291.1:g.18853A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1448A= MANE Select	ENSP00000295897.4:p.Gln483=
ENST00000295897.8:c.1448A=	ENSP00000295897.4:p.Gln483=
ENST00000401494.7:c.1103A=	ENSP00000384695.3:p.Gln368=
ENST00000415165.6:c.872A=	ENSP00000401820.2:p.Gln291=
ENST00000476441.6:c.*727A=	ENSP00000423727.1:n.*727A=
ENST00000486939.1:n.102A=
ENST00000503124.5:c.998A=	ENSP00000421027.1:p.Gln333=
ENST00000505649.5:n.995A=
ENST00000509063.5:c.1448A=	ENSP00000422784.1:p.Gln483=
ENST00000511370.1:c.981A=
ENST00000621085.4:c.809A=	ENSP00000483421.1:p.Gln270=
ENST00000621628.4:c.809A=	ENSP00000480485.1:p.Gln270=
NM_000477.5:c.1448A=	NP_000468.1:p.Gln483=
NM_000477.6:c.1448A=	NP_000468.1:p.Gln483=
NM_000477.7:c.1448A= MANE Select	NP_000468.1:p.Gln483=