Canonical Allele Identifier: CA357240570

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74279184T>A (hg19) ; chr4:g.73413467T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413467T>A , CM000666.2:g.73413467T>A	GRCh38
NC_000004.11:g.74279184T>A , CM000666.1:g.74279184T>A	GRCh37
NC_000004.10:g.74498048T>A	NCBI36
NG_009291.1:g.14213T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.891T>A MANE Select	ENSP00000295897.4:p.Ser297Arg
ENST00000295897.8:c.891T>A	ENSP00000295897.4:p.Ser297Arg
ENST00000401494.7:c.546T>A	ENSP00000384695.3:p.Ser182Arg
ENST00000415165.6:c.315T>A	ENSP00000401820.2:p.Ser105Arg
ENST00000476441.6:c.*170T>A	ENSP00000423727.1:n.*170T>A
ENST00000484992.1:n.211T>A
ENST00000503124.5:c.441T>A	ENSP00000421027.1:p.Ser147Arg
ENST00000505649.5:n.577T>A
ENST00000509063.5:c.891T>A	ENSP00000422784.1:p.Ser297Arg
ENST00000511370.1:c.424T>A
ENST00000621085.4:c.491-1639T>A	ENSP00000483421.1:n.491-1639T>A
ENST00000621628.4:c.487-1635T>A	ENSP00000480485.1:n.487-1635T>A
NM_000477.5:c.891T>A	NP_000468.1:p.Ser297Arg
NM_000477.6:c.891T>A	NP_000468.1:p.Ser297Arg
NM_000477.7:c.891T>A MANE Select	NP_000468.1:p.Ser297Arg