Canonical Allele Identifier: CA645517877

Gene: ALB

Linked Data

• COSMIC: COSM4950955 ; COSM5348346

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420291del , CM000666.2:g.73420291del	GRCh38
NC_000004.11:g.74286008del , CM000666.1:g.74286008del	GRCh37
NC_000004.10:g.74504872del	NCBI36
NG_009291.1:g.21037del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1823del MANE Select	ENSP00000295897.4:p.Gly608AlafsTer?
ENST00000295897.8:c.1823del	ENSP00000295897.4:p.Gly608AlafsTer?
ENST00000401494.7:c.1478del	ENSP00000384695.3:p.Gly493AlafsTer?
ENST00000415165.6:c.1247del	ENSP00000401820.2:p.Gly416AlafsTer?
ENST00000476441.6:c.*1102del	ENSP00000423727.1:n.*1102del
ENST00000495173.1:n.131del
ENST00000503124.5:c.1373del	ENSP00000421027.1:p.Gly458AlafsTer?
ENST00000505649.5:n.1370del
ENST00000508932.5:n.213del
ENST00000509063.5:c.1785+652del	ENSP00000422784.1:n.1785+652del
ENST00000511370.1:c.1356del
ENST00000621085.4:c.1184del	ENSP00000483421.1:p.Gly395AlafsTer?
ENST00000621628.4:c.1184del	ENSP00000480485.1:p.Gly395AlafsTer?
NM_000477.5:c.1823del	NP_000468.1:p.Gly608AlafsTer?
NM_000477.6:c.1823del	NP_000468.1:p.Gly608AlafsTer?
NM_000477.7:c.1823del MANE Select	NP_000468.1:p.Gly608AlafsTer?