Canonical Allele Identifier: CA357235997

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74272456C>A (hg19) ; chr4:g.73406739C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406739C>A , CM000666.2:g.73406739C>A	GRCh38
NC_000004.11:g.74272456C>A , CM000666.1:g.74272456C>A	GRCh37
NC_000004.10:g.74491320C>A	NCBI36
NG_009291.1:g.7485C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.248C>A MANE Select	ENSP00000295897.4:p.Ala83Asp
ENST00000295897.8:c.248C>A	ENSP00000295897.4:p.Ala83Asp
ENST00000401494.7:c.137+1566C>A	ENSP00000384695.3:n.137+1566C>A
ENST00000415165.6:c.137+1566C>A	ENSP00000401820.2:n.137+1566C>A
ENST00000441319.5:c.254C>A	ENSP00000392541.1:p.Ala85Asp
ENST00000476441.6:c.79+2333C>A	ENSP00000423727.1:n.79+2333C>A
ENST00000503124.5:c.10C>A	ENSP00000421027.1:p.Leu4Met
ENST00000509063.5:c.248C>A	ENSP00000422784.1:p.Ala83Asp
ENST00000510166.5:n.284C>A
ENST00000514786.1:n.217C>A
ENST00000515133.5:n.289C>A
ENST00000621085.4:c.248C>A	ENSP00000483421.1:p.Ala83Asp
ENST00000621628.4:c.248C>A	ENSP00000480485.1:p.Ala83Asp
NM_000477.5:c.248C>A	NP_000468.1:p.Ala83Asp
NM_000477.6:c.248C>A	NP_000468.1:p.Ala83Asp
NM_000477.7:c.248C>A MANE Select	NP_000468.1:p.Ala83Asp