Canonical Allele Identifier: CA648962970

Gene: ALB

Linked Data

• COSMIC: COSN2044086

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409330_73409333del , CM000666.2:g.73409330_73409333del	GRCh38
NC_000004.11:g.74275047_74275050del , CM000666.1:g.74275047_74275050del	GRCh37
NC_000004.10:g.74493911_74493914del	NCBI36
NG_009291.1:g.10076_10079del

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.483-25_483-22del MANE Select	ENSP00000295897.4:n.483-25_483-22del
ENST00000295897.8:c.483-25_483-22del	ENSP00000295897.4:n.483-25_483-22del
ENST00000401494.7:c.138-25_138-22del	ENSP00000384695.3:n.138-25_138-22del
ENST00000415165.6:c.138-2666_138-2663del	ENSP00000401820.2:n.138-2666_138-2663del
ENST00000441319.5:c.489-25_489-22del	ENSP00000392541.1:n.489-25_489-22del
ENST00000476441.6:c.80-25_80-22del	ENSP00000423727.1:n.80-25_80-22del
ENST00000503124.5:c.33-25_33-22del	ENSP00000421027.1:n.33-25_33-22del
ENST00000505649.5:n.169-25_169-22del
ENST00000509063.5:c.483-25_483-22del	ENSP00000422784.1:n.483-25_483-22del
ENST00000514786.1:n.452-25_452-22del
ENST00000621085.4:c.483-25_483-22del	ENSP00000483421.1:n.483-25_483-22del
ENST00000621628.4:c.486+254_486+257del	ENSP00000480485.1:n.486+254_486+257del
NM_000477.5:c.483-25_483-22del	NP_000468.1:n.483-25_483-22del
NM_000477.6:c.483-25_483-22del	NP_000468.1:n.483-25_483-22del
NM_000477.7:c.483-25_483-22del MANE Select	NP_000468.1:n.483-25_483-22del