Canonical Allele Identifier: CA357235895

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74272444C>A (hg19) ; chr4:g.73406727C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406727C>A , CM000666.2:g.73406727C>A	GRCh38
NC_000004.11:g.74272444C>A , CM000666.1:g.74272444C>A	GRCh37
NC_000004.10:g.74491308C>A	NCBI36
NG_009291.1:g.7473C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.236C>A MANE Select	ENSP00000295897.4:p.Ala79Asp
ENST00000295897.8:c.236C>A	ENSP00000295897.4:p.Ala79Asp
ENST00000401494.7:c.137+1554C>A	ENSP00000384695.3:n.137+1554C>A
ENST00000415165.6:c.137+1554C>A	ENSP00000401820.2:n.137+1554C>A
ENST00000441319.5:c.242C>A	ENSP00000392541.1:p.Ala81Asp
ENST00000476441.6:c.79+2321C>A	ENSP00000423727.1:n.79+2321C>A
ENST00000503124.5:c.-3C>A	ENSP00000421027.1:n.-3C>A
ENST00000509063.5:c.236C>A	ENSP00000422784.1:p.Ala79Asp
ENST00000510166.5:n.272C>A
ENST00000514786.1:n.205C>A
ENST00000515133.5:n.277C>A
ENST00000621085.4:c.236C>A	ENSP00000483421.1:p.Ala79Asp
ENST00000621628.4:c.236C>A	ENSP00000480485.1:p.Ala79Asp
NM_000477.5:c.236C>A	NP_000468.1:p.Ala79Asp
NM_000477.6:c.236C>A	NP_000468.1:p.Ala79Asp
NM_000477.7:c.236C>A MANE Select	NP_000468.1:p.Ala79Asp