Canonical Allele Identifier: CA1468143577

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415131T= , CM000666.2:g.73415131T=	GRCh38
NC_000004.11:g.74280848T= , CM000666.1:g.74280848T=	GRCh37
NC_000004.10:g.74499712T=	NCBI36
NG_009291.1:g.15877T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1155T= MANE Select	ENSP00000295897.4:p.Cys385=
ENST00000295897.8:c.1155T=	ENSP00000295897.4:p.Cys385=
ENST00000401494.7:c.810T=	ENSP00000384695.3:p.Cys270=
ENST00000415165.6:c.579T=	ENSP00000401820.2:p.Cys193=
ENST00000476441.6:c.*434T=	ENSP00000423727.1:n.*434T=
ENST00000484992.1:n.475T=
ENST00000503124.5:c.705T=	ENSP00000421027.1:p.Cys235=
ENST00000504043.1:n.158T=
ENST00000505649.5:n.841T=
ENST00000509063.5:c.1155T=	ENSP00000422784.1:p.Cys385=
ENST00000511370.1:c.688T=
ENST00000621085.4:c.516T=	ENSP00000483421.1:p.Cys172=
ENST00000621628.4:c.516T=	ENSP00000480485.1:p.Cys172=
NM_000477.5:c.1155T=	NP_000468.1:p.Cys385=
NM_000477.6:c.1155T=	NP_000468.1:p.Cys385=
NM_000477.7:c.1155T= MANE Select	NP_000468.1:p.Cys385=