Canonical Allele Identifier: CA357236141

Gene: ALB

Linked Data

• COSMIC: COSM4952306
• MyVariant Identifiers: chr4:g.74272474C>A (hg19) ; chr4:g.73406757C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406757C>A , CM000666.2:g.73406757C>A	GRCh38
NC_000004.11:g.74272474C>A , CM000666.1:g.74272474C>A	GRCh37
NC_000004.10:g.74491338C>A	NCBI36
NG_009291.1:g.7503C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.266C>A MANE Select	ENSP00000295897.4:p.Ser89Ter
ENST00000295897.8:c.266C>A	ENSP00000295897.4:p.Ser89Ter
ENST00000401494.7:c.137+1584C>A	ENSP00000384695.3:n.137+1584C>A
ENST00000415165.6:c.137+1584C>A	ENSP00000401820.2:n.137+1584C>A
ENST00000441319.5:c.272C>A	ENSP00000392541.1:p.Ser91Ter
ENST00000476441.6:c.79+2351C>A	ENSP00000423727.1:n.79+2351C>A
ENST00000503124.5:c.28C>A	ENSP00000421027.1:p.His10Asn
ENST00000509063.5:c.266C>A	ENSP00000422784.1:p.Ser89Ter
ENST00000510166.5:n.302C>A
ENST00000514786.1:n.235C>A
ENST00000515133.5:n.307C>A
ENST00000621085.4:c.266C>A	ENSP00000483421.1:p.Ser89Ter
ENST00000621628.4:c.266C>A	ENSP00000480485.1:p.Ser89Ter
NM_000477.5:c.266C>A	NP_000468.1:p.Ser89Ter
NM_000477.6:c.266C>A	NP_000468.1:p.Ser89Ter
NM_000477.7:c.266C>A MANE Select	NP_000468.1:p.Ser89Ter