Canonical Allele Identifier: CA357244191

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74283833T>A (hg19) ; chr4:g.73418116T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418116T>A , CM000666.2:g.73418116T>A	GRCh38
NC_000004.11:g.74283833T>A , CM000666.1:g.74283833T>A	GRCh37
NC_000004.10:g.74502697T>A	NCBI36
NG_009291.1:g.18862T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1457T>A MANE Select	ENSP00000295897.4:p.Val486Glu
ENST00000295897.8:c.1457T>A	ENSP00000295897.4:p.Val486Glu
ENST00000401494.7:c.1112T>A	ENSP00000384695.3:p.Val371Glu
ENST00000415165.6:c.881T>A	ENSP00000401820.2:p.Val294Glu
ENST00000476441.6:c.*736T>A	ENSP00000423727.1:n.*736T>A
ENST00000486939.1:n.111T>A
ENST00000503124.5:c.1007T>A	ENSP00000421027.1:p.Val336Glu
ENST00000505649.5:n.1004T>A
ENST00000509063.5:c.1457T>A	ENSP00000422784.1:p.Val486Glu
ENST00000511370.1:c.990T>A
ENST00000621085.4:c.818T>A	ENSP00000483421.1:p.Val273Glu
ENST00000621628.4:c.818T>A	ENSP00000480485.1:p.Val273Glu
NM_000477.5:c.1457T>A	NP_000468.1:p.Val486Glu
NM_000477.6:c.1457T>A	NP_000468.1:p.Val486Glu
NM_000477.7:c.1457T>A MANE Select	NP_000468.1:p.Val486Glu