Canonical Allele Identifier: CA357240615

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74279195A>T (hg19) ; chr4:g.73413478A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413478A>T , CM000666.2:g.73413478A>T	GRCh38
NC_000004.11:g.74279195A>T , CM000666.1:g.74279195A>T	GRCh37
NC_000004.10:g.74498059A>T	NCBI36
NG_009291.1:g.14224A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.902A>T MANE Select	ENSP00000295897.4:p.Glu301Val
ENST00000295897.8:c.902A>T	ENSP00000295897.4:p.Glu301Val
ENST00000401494.7:c.557A>T	ENSP00000384695.3:p.Glu186Val
ENST00000415165.6:c.326A>T	ENSP00000401820.2:p.Glu109Val
ENST00000476441.6:c.*181A>T	ENSP00000423727.1:n.*181A>T
ENST00000484992.1:n.222A>T
ENST00000503124.5:c.452A>T	ENSP00000421027.1:p.Glu151Val
ENST00000505649.5:n.588A>T
ENST00000509063.5:c.902A>T	ENSP00000422784.1:p.Glu301Val
ENST00000511370.1:c.435A>T
ENST00000621085.4:c.491-1628A>T	ENSP00000483421.1:n.491-1628A>T
ENST00000621628.4:c.487-1624A>T	ENSP00000480485.1:n.487-1624A>T
NM_000477.5:c.902A>T	NP_000468.1:p.Glu301Val
NM_000477.6:c.902A>T	NP_000468.1:p.Glu301Val
NM_000477.7:c.902A>T MANE Select	NP_000468.1:p.Glu301Val