Canonical Allele Identifier: CA648962892

Gene: ALB

Linked Data

• COSMIC: COSN1300831

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409036_73409037del , CM000666.2:g.73409036_73409037del	GRCh38
NC_000004.11:g.74274753_74274754del , CM000666.1:g.74274753_74274754del	GRCh37
NC_000004.10:g.74493617_74493618del	NCBI36
NG_009291.1:g.9782_9783del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.482+231_482+232del MANE Select	ENSP00000295897.4:n.482+231_482+232del
ENST00000295897.8:c.482+231_482+232del	ENSP00000295897.4:n.482+231_482+232del
ENST00000401494.7:c.138-319_138-318del	ENSP00000384695.3:n.138-319_138-318del
ENST00000415165.6:c.138-2960_138-2959del	ENSP00000401820.2:n.138-2960_138-2959del
ENST00000441319.5:c.488+231_488+232del	ENSP00000392541.1:n.488+231_488+232del
ENST00000476441.6:c.80-319_80-318del	ENSP00000423727.1:n.80-319_80-318del
ENST00000503124.5:c.33-319_33-318del	ENSP00000421027.1:n.33-319_33-318del
ENST00000505649.5:n.168+231_168+232del
ENST00000509063.5:c.482+231_482+232del	ENSP00000422784.1:n.482+231_482+232del
ENST00000514786.1:n.451+231_451+232del
ENST00000621085.4:c.482+231_482+232del	ENSP00000483421.1:n.482+231_482+232del
ENST00000621628.4:c.483-37_483-36del	ENSP00000480485.1:n.483-37_483-36del
NM_000477.5:c.482+231_482+232del	NP_000468.1:n.482+231_482+232del
NM_000477.6:c.482+231_482+232del	NP_000468.1:n.482+231_482+232del
NM_000477.7:c.482+231_482+232del MANE Select	NP_000468.1:n.482+231_482+232del