Canonical Allele Identifier: CA645517836

Gene: ALB

Linked Data

• COSMIC: COSM5347701

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406675_73406676del , CM000666.2:g.73406675_73406676del	GRCh38
NC_000004.11:g.74272392_74272393del , CM000666.1:g.74272392_74272393del	GRCh37
NC_000004.10:g.74491256_74491257del	NCBI36
NG_009291.1:g.7421_7422del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.184_185del MANE Select	ENSP00000295897.4:p.Asp62SerfsTer7
ENST00000295897.8:c.184_185del	ENSP00000295897.4:p.Asp62SerfsTer7
ENST00000401494.7:c.137+1502_137+1503del	ENSP00000384695.3:n.137+1502_137+1503del
ENST00000415165.6:c.137+1502_137+1503del	ENSP00000401820.2:n.137+1502_137+1503del
ENST00000441319.5:c.190_191del	ENSP00000392541.1:p.Asp64SerfsTer7
ENST00000476441.6:c.79+2269_79+2270del	ENSP00000423727.1:n.79+2269_79+2270del
ENST00000503124.5:c.-55_-54del	ENSP00000421027.1:n.-55_-54del
ENST00000509063.5:c.184_185del	ENSP00000422784.1:p.Asp62SerfsTer7
ENST00000510166.5:n.220_221del
ENST00000514786.1:n.153_154del
ENST00000515133.5:n.225_226del
ENST00000621085.4:c.184_185del	ENSP00000483421.1:p.Asp62SerfsTer7
ENST00000621628.4:c.184_185del	ENSP00000480485.1:p.Asp62SerfsTer7
NM_000477.5:c.184_185del	NP_000468.1:p.Asp62SerfsTer7
NM_000477.6:c.184_185del	NP_000468.1:p.Asp62SerfsTer7
NM_000477.7:c.184_185del MANE Select	NP_000468.1:p.Asp62SerfsTer7