Canonical Allele Identifier: CA1468150891

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406677T= , CM000666.2:g.73406677T=	GRCh38
NC_000004.11:g.74272394T= , CM000666.1:g.74272394T=	GRCh37
NC_000004.10:g.74491258T=	NCBI36
NG_009291.1:g.7423T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.186T= MANE Select	ENSP00000295897.4:p.Asp62=
ENST00000295897.8:c.186T=	ENSP00000295897.4:p.Asp62=
ENST00000401494.7:c.137+1504T=	ENSP00000384695.3:n.137+1504T=
ENST00000415165.6:c.137+1504T=	ENSP00000401820.2:n.137+1504T=
ENST00000441319.5:c.192T=	ENSP00000392541.1:p.Asp64=
ENST00000476441.6:c.79+2271T=	ENSP00000423727.1:n.79+2271T=
ENST00000503124.5:c.-53T=	ENSP00000421027.1:n.-53T=
ENST00000509063.5:c.186T=	ENSP00000422784.1:p.Asp62=
ENST00000510166.5:n.222T=
ENST00000514786.1:n.155T=
ENST00000515133.5:n.227T=
ENST00000621085.4:c.186T=	ENSP00000483421.1:p.Asp62=
ENST00000621628.4:c.186T=	ENSP00000480485.1:p.Asp62=
NM_000477.5:c.186T=	NP_000468.1:p.Asp62=
NM_000477.6:c.186T=	NP_000468.1:p.Asp62=
NM_000477.7:c.186T= MANE Select	NP_000468.1:p.Asp62=