Canonical Allele Identifier: CA1468143554

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415120G= , CM000666.2:g.73415120G=	GRCh38
NC_000004.11:g.74280837G= , CM000666.1:g.74280837G=	GRCh37
NC_000004.10:g.74499701G=	NCBI36
NG_009291.1:g.15866G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1144G= MANE Select	ENSP00000295897.4:p.Glu382=
ENST00000295897.8:c.1144G=	ENSP00000295897.4:p.Glu382=
ENST00000401494.7:c.799G=	ENSP00000384695.3:p.Glu267=
ENST00000415165.6:c.568G=	ENSP00000401820.2:p.Glu190=
ENST00000476441.6:c.*423G=	ENSP00000423727.1:n.*423G=
ENST00000484992.1:n.464G=
ENST00000503124.5:c.694G=	ENSP00000421027.1:p.Glu232=
ENST00000504043.1:n.147G=
ENST00000505649.5:n.830G=
ENST00000509063.5:c.1144G=	ENSP00000422784.1:p.Glu382=
ENST00000511370.1:c.677G=
ENST00000621085.4:c.505G=	ENSP00000483421.1:p.Glu169=
ENST00000621628.4:c.505G=	ENSP00000480485.1:p.Glu169=
NM_000477.5:c.1144G=	NP_000468.1:p.Glu382=
NM_000477.6:c.1144G=	NP_000468.1:p.Glu382=
NM_000477.7:c.1144G= MANE Select	NP_000468.1:p.Glu382=