Canonical Allele Identifier: CA1468143571

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415126T= , CM000666.2:g.73415126T=	GRCh38
NC_000004.11:g.74280843T= , CM000666.1:g.74280843T=	GRCh37
NC_000004.10:g.74499707T=	NCBI36
NG_009291.1:g.15872T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1150T= MANE Select	ENSP00000295897.4:p.Cys384=
ENST00000295897.8:c.1150T=	ENSP00000295897.4:p.Cys384=
ENST00000401494.7:c.805T=	ENSP00000384695.3:p.Cys269=
ENST00000415165.6:c.574T=	ENSP00000401820.2:p.Cys192=
ENST00000476441.6:c.*429T=	ENSP00000423727.1:n.*429T=
ENST00000484992.1:n.470T=
ENST00000503124.5:c.700T=	ENSP00000421027.1:p.Cys234=
ENST00000504043.1:n.153T=
ENST00000505649.5:n.836T=
ENST00000509063.5:c.1150T=	ENSP00000422784.1:p.Cys384=
ENST00000511370.1:c.683T=
ENST00000621085.4:c.511T=	ENSP00000483421.1:p.Cys171=
ENST00000621628.4:c.511T=	ENSP00000480485.1:p.Cys171=
NM_000477.5:c.1150T=	NP_000468.1:p.Cys384=
NM_000477.6:c.1150T=	NP_000468.1:p.Cys384=
NM_000477.7:c.1150T= MANE Select	NP_000468.1:p.Cys384=