Canonical Allele Identifier: CA645517838

Gene: ALB

Linked Data

• COSMIC: COSM5347703 ; COSM6240377

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408810_73408813del , CM000666.2:g.73408810_73408813del	GRCh38
NC_000004.11:g.74274527_74274530del , CM000666.1:g.74274527_74274530del	GRCh37
NC_000004.10:g.74493391_74493394del	NCBI36
NG_009291.1:g.9556_9559del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.482+5_482+8del
ENST00000295897.8:c.482+5_482+8del
ENST00000401494.7:c.138-545_138-542del	ENSP00000384695.3:n.138-545_138-542del
ENST00000415165.6:c.138-3186_138-3183del	ENSP00000401820.2:n.138-3186_138-3183del
ENST00000441319.5:c.488+5_488+8del
ENST00000476441.6:c.80-545_80-542del	ENSP00000423727.1:n.80-545_80-542del
ENST00000503124.5:c.33-545_33-542del	ENSP00000421027.1:n.33-545_33-542del
ENST00000505649.5:n.168+5_168+8del
ENST00000509063.5:c.482+5_482+8del
ENST00000510166.5:n.523_526del
ENST00000514786.1:n.451+5_451+8del
ENST00000515133.5:n.528_531del
ENST00000621085.4:c.482+5_482+8del
ENST00000621628.4:c.482+5_482+8del
NM_000477.5:c.482+5_482+8del
NM_000477.6:c.482+5_482+8del
NM_000477.7:c.482+5_482+8del