Canonical Allele Identifier: CA648962930

Gene: ALB

Linked Data

• COSMIC: COSN24900245

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409298_73409300del , CM000666.2:g.73409298_73409300del	GRCh38
NC_000004.11:g.74275015_74275017del , CM000666.1:g.74275015_74275017del	GRCh37
NC_000004.10:g.74493879_74493881del	NCBI36
NG_009291.1:g.10044_10046del

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.483-57_483-55del MANE Select	ENSP00000295897.4:n.483-57_483-55del
ENST00000295897.8:c.483-57_483-55del	ENSP00000295897.4:n.483-57_483-55del
ENST00000401494.7:c.138-57_138-55del	ENSP00000384695.3:n.138-57_138-55del
ENST00000415165.6:c.138-2698_138-2696del	ENSP00000401820.2:n.138-2698_138-2696del
ENST00000441319.5:c.489-57_489-55del	ENSP00000392541.1:n.489-57_489-55del
ENST00000476441.6:c.80-57_80-55del	ENSP00000423727.1:n.80-57_80-55del
ENST00000503124.5:c.33-57_33-55del	ENSP00000421027.1:n.33-57_33-55del
ENST00000505649.5:n.169-57_169-55del
ENST00000509063.5:c.483-57_483-55del	ENSP00000422784.1:n.483-57_483-55del
ENST00000514786.1:n.452-57_452-55del
ENST00000621085.4:c.483-57_483-55del	ENSP00000483421.1:n.483-57_483-55del
ENST00000621628.4:c.486+222_486+224del	ENSP00000480485.1:n.486+222_486+224del
NM_000477.5:c.483-57_483-55del	NP_000468.1:n.483-57_483-55del
NM_000477.6:c.483-57_483-55del	NP_000468.1:n.483-57_483-55del
NM_000477.7:c.483-57_483-55del MANE Select	NP_000468.1:n.483-57_483-55del