Canonical Allele Identifier: CA357240533

Gene: ALB

Linked Data

• COSMIC: COSM6023366
• MyVariant Identifiers: chr4:g.74279174C>A (hg19) ; chr4:g.73413457C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413457C>A , CM000666.2:g.73413457C>A	GRCh38
NC_000004.11:g.74279174C>A , CM000666.1:g.74279174C>A	GRCh37
NC_000004.10:g.74498038C>A	NCBI36
NG_009291.1:g.14203C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.881C>A MANE Select	ENSP00000295897.4:p.Ser294Ter
ENST00000295897.8:c.881C>A	ENSP00000295897.4:p.Ser294Ter
ENST00000401494.7:c.536C>A	ENSP00000384695.3:p.Ser179Ter
ENST00000415165.6:c.305C>A	ENSP00000401820.2:p.Ser102Ter
ENST00000476441.6:c.*160C>A	ENSP00000423727.1:n.*160C>A
ENST00000484992.1:n.201C>A
ENST00000503124.5:c.431C>A	ENSP00000421027.1:p.Ser144Ter
ENST00000505649.5:n.567C>A
ENST00000509063.5:c.881C>A	ENSP00000422784.1:p.Ser294Ter
ENST00000511370.1:c.414C>A
ENST00000621085.4:c.491-1649C>A	ENSP00000483421.1:n.491-1649C>A
ENST00000621628.4:c.487-1645C>A	ENSP00000480485.1:n.487-1645C>A
NM_000477.5:c.881C>A	NP_000468.1:p.Ser294Ter
NM_000477.6:c.881C>A	NP_000468.1:p.Ser294Ter
NM_000477.7:c.881C>A MANE Select	NP_000468.1:p.Ser294Ter