Canonical Allele Identifier: CA1468146918

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418223G= , CM000666.2:g.73418223G=	GRCh38
NC_000004.11:g.74283940G= , CM000666.1:g.74283940G=	GRCh37
NC_000004.10:g.74502804G=	NCBI36
NG_009291.1:g.18969G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1564G= MANE Select	ENSP00000295897.4:p.Val522=
ENST00000295897.8:c.1564G=	ENSP00000295897.4:p.Val522=
ENST00000401494.7:c.1219G=	ENSP00000384695.3:p.Val407=
ENST00000415165.6:c.988G=	ENSP00000401820.2:p.Val330=
ENST00000476441.6:c.*843G=	ENSP00000423727.1:n.*843G=
ENST00000486939.1:n.218G=
ENST00000503124.5:c.1114G=	ENSP00000421027.1:p.Val372=
ENST00000505649.5:n.1111G=
ENST00000509063.5:c.1564G=	ENSP00000422784.1:p.Val522=
ENST00000511370.1:c.1097G=
ENST00000621085.4:c.925G=	ENSP00000483421.1:p.Val309=
ENST00000621628.4:c.925G=	ENSP00000480485.1:p.Val309=
NM_000477.5:c.1564G=	NP_000468.1:p.Val522=
NM_000477.6:c.1564G=	NP_000468.1:p.Val522=
NM_000477.7:c.1564G= MANE Select	NP_000468.1:p.Val522=