Canonical Allele Identifier: CA648962669

Gene: ALB

Linked Data

• COSMIC: COSN24910388

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406832_73406835del , CM000666.2:g.73406832_73406835del	GRCh38
NC_000004.11:g.74272549_74272552del , CM000666.1:g.74272549_74272552del	GRCh37
NC_000004.10:g.74491413_74491416del	NCBI36
NG_009291.1:g.7578_7581del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.270+71_270+74del MANE Select	ENSP00000295897.4:n.270+71_270+74del
ENST00000295897.8:c.270+71_270+74del	ENSP00000295897.4:n.270+71_270+74del
ENST00000401494.7:c.137+1659_137+1662del	ENSP00000384695.3:n.137+1659_137+1662del
ENST00000415165.6:c.137+1659_137+1662del	ENSP00000401820.2:n.137+1659_137+1662del
ENST00000441319.5:c.276+71_276+74del	ENSP00000392541.1:n.276+71_276+74del
ENST00000476441.6:c.79+2426_79+2429del	ENSP00000423727.1:n.79+2426_79+2429del
ENST00000503124.5:c.32+71_32+74del	ENSP00000421027.1:n.32+71_32+74del
ENST00000509063.5:c.270+71_270+74del	ENSP00000422784.1:n.270+71_270+74del
ENST00000510166.5:n.306+71_306+74del
ENST00000514786.1:n.239+71_239+74del
ENST00000515133.5:n.311+71_311+74del
ENST00000621085.4:c.270+71_270+74del	ENSP00000483421.1:n.270+71_270+74del
ENST00000621628.4:c.270+71_270+74del	ENSP00000480485.1:n.270+71_270+74del
NM_000477.5:c.270+71_270+74del	NP_000468.1:n.270+71_270+74del
NM_000477.6:c.270+71_270+74del	NP_000468.1:n.270+71_270+74del
NM_000477.7:c.270+71_270+74del MANE Select	NP_000468.1:n.270+71_270+74del