Canonical Allele Identifier: CA1468146972

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418269T= , CM000666.2:g.73418269T=	GRCh38
NC_000004.11:g.74283986T= , CM000666.1:g.74283986T=	GRCh37
NC_000004.10:g.74502850T=	NCBI36
NG_009291.1:g.19015T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000477.7:c.1610T= MANE Select	NP_000468.1:p.Ile537=
ENST00000295897.9:c.1610T= MANE Select	ENSP00000295897.4:p.Ile537=
NM_000477.5:c.1610T=	NP_000468.1:p.Ile537=
NM_000477.6:c.1610T=	NP_000468.1:p.Ile537=
ENST00000295897.8:c.1610T=	ENSP00000295897.4:p.Ile537=
ENST00000401494.7:c.1265T=	ENSP00000384695.3:p.Ile422=
ENST00000415165.6:c.1034T=	ENSP00000401820.2:p.Ile345=
ENST00000476441.6:c.*889T=	ENSP00000423727.1:n.*889T=
ENST00000486939.1:n.264T=
ENST00000503124.5:c.1160T=	ENSP00000421027.1:p.Ile387=
ENST00000505649.5:n.1157T=
ENST00000509063.5:c.1610T=	ENSP00000422784.1:p.Ile537=
ENST00000511370.1:c.1143T=
ENST00000621085.4:c.971T=	ENSP00000483421.1:p.Ile324=
ENST00000621628.4:c.971T=	ENSP00000480485.1:p.Ile324=