Canonical Allele Identifier: CA1468143472

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415076T= , CM000666.2:g.73415076T=	GRCh38
NC_000004.11:g.74280793T= , CM000666.1:g.74280793T=	GRCh37
NC_000004.10:g.74499657T=	NCBI36
NG_009291.1:g.15822T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1100T= MANE Select	ENSP00000295897.4:p.Val367=
ENST00000295897.8:c.1100T=	ENSP00000295897.4:p.Val367=
ENST00000401494.7:c.755T=	ENSP00000384695.3:p.Val252=
ENST00000415165.6:c.524T=	ENSP00000401820.2:p.Val175=
ENST00000476441.6:c.*379T=	ENSP00000423727.1:n.*379T=
ENST00000484992.1:n.420T=
ENST00000503124.5:c.650T=	ENSP00000421027.1:p.Val217=
ENST00000504043.1:n.103T=
ENST00000505649.5:n.786T=
ENST00000509063.5:c.1100T=	ENSP00000422784.1:p.Val367=
ENST00000511370.1:c.633T=
ENST00000621085.4:c.491-30T=	ENSP00000483421.1:n.491-30T=
ENST00000621628.4:c.487-26T=	ENSP00000480485.1:n.487-26T=
NM_000477.5:c.1100T=	NP_000468.1:p.Val367=
NM_000477.6:c.1100T=	NP_000468.1:p.Val367=
NM_000477.7:c.1100T= MANE Select	NP_000468.1:p.Val367=