Canonical Allele Identifier: CA357236109

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74272468A>T (hg19) ; chr4:g.73406751A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406751A>T , CM000666.2:g.73406751A>T	GRCh38
NC_000004.11:g.74272468A>T , CM000666.1:g.74272468A>T	GRCh37
NC_000004.10:g.74491332A>T	NCBI36
NG_009291.1:g.7497A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.260A>T MANE Select	ENSP00000295897.4:p.Asp87Val
ENST00000295897.8:c.260A>T	ENSP00000295897.4:p.Asp87Val
ENST00000401494.7:c.137+1578A>T	ENSP00000384695.3:n.137+1578A>T
ENST00000415165.6:c.137+1578A>T	ENSP00000401820.2:n.137+1578A>T
ENST00000441319.5:c.266A>T	ENSP00000392541.1:p.Asp89Val
ENST00000476441.6:c.79+2345A>T	ENSP00000423727.1:n.79+2345A>T
ENST00000503124.5:c.22A>T	ENSP00000421027.1:p.Thr8Ser
ENST00000509063.5:c.260A>T	ENSP00000422784.1:p.Asp87Val
ENST00000510166.5:n.296A>T
ENST00000514786.1:n.229A>T
ENST00000515133.5:n.301A>T
ENST00000621085.4:c.260A>T	ENSP00000483421.1:p.Asp87Val
ENST00000621628.4:c.260A>T	ENSP00000480485.1:p.Asp87Val
NM_000477.5:c.260A>T	NP_000468.1:p.Asp87Val
NM_000477.6:c.260A>T	NP_000468.1:p.Asp87Val
NM_000477.7:c.260A>T MANE Select	NP_000468.1:p.Asp87Val