Canonical Allele Identifier: CA1468146806

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418137T= , CM000666.2:g.73418137T=	GRCh38
NC_000004.11:g.74283854T= , CM000666.1:g.74283854T=	GRCh37
NC_000004.10:g.74502718T=	NCBI36
NG_009291.1:g.18883T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1478T= MANE Select	ENSP00000295897.4:p.Val493=
ENST00000295897.8:c.1478T=	ENSP00000295897.4:p.Val493=
ENST00000401494.7:c.1133T=	ENSP00000384695.3:p.Val378=
ENST00000415165.6:c.902T=	ENSP00000401820.2:p.Val301=
ENST00000476441.6:c.*757T=	ENSP00000423727.1:n.*757T=
ENST00000486939.1:n.132T=
ENST00000503124.5:c.1028T=	ENSP00000421027.1:p.Val343=
ENST00000505649.5:n.1025T=
ENST00000509063.5:c.1478T=	ENSP00000422784.1:p.Val493=
ENST00000511370.1:c.1011T=
ENST00000621085.4:c.839T=	ENSP00000483421.1:p.Val280=
ENST00000621628.4:c.839T=	ENSP00000480485.1:p.Val280=
NM_000477.5:c.1478T=	NP_000468.1:p.Val493=
NM_000477.6:c.1478T=	NP_000468.1:p.Val493=
NM_000477.7:c.1478T= MANE Select	NP_000468.1:p.Val493=