Canonical Allele Identifier: CA1468143543

Gene: ALB

Linked Data

• dbSNP Id: rs1718980848

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415114del , CM000666.2:g.73415114del	GRCh38
NC_000004.11:g.74280831del , CM000666.1:g.74280831del	GRCh37
NC_000004.10:g.74499695del	NCBI36
NG_009291.1:g.15860del

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1138del MANE Select	ENSP00000295897.4:p.Thr380LeufsTer2
ENST00000295897.8:c.1138del	ENSP00000295897.4:p.Thr380LeufsTer2
ENST00000401494.7:c.793del	ENSP00000384695.3:p.Thr265LeufsTer2
ENST00000415165.6:c.562del	ENSP00000401820.2:p.Thr188LeufsTer2
ENST00000476441.6:c.*417del	ENSP00000423727.1:n.*417del
ENST00000484992.1:n.458del
ENST00000503124.5:c.688del	ENSP00000421027.1:p.Thr230LeufsTer2
ENST00000504043.1:n.141del
ENST00000505649.5:n.824del
ENST00000509063.5:c.1138del	ENSP00000422784.1:p.Thr380LeufsTer2
ENST00000511370.1:c.671del
ENST00000621085.4:c.499del	ENSP00000483421.1:p.Thr167LeufsTer2
ENST00000621628.4:c.499del	ENSP00000480485.1:p.Thr167LeufsTer2
NM_000477.5:c.1138del	NP_000468.1:p.Thr380LeufsTer2
NM_000477.6:c.1138del	NP_000468.1:p.Thr380LeufsTer2
NM_000477.7:c.1138del MANE Select	NP_000468.1:p.Thr380LeufsTer2