Canonical Allele Identifier: CA645517839
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73408805_73408806del , CM000666.2:g.73408805_73408806del GRCh38
NC_000004.11:g.74274522_74274523del , CM000666.1:g.74274522_74274523del GRCh37
NC_000004.10:g.74493386_74493387del NCBI36
NG_009291.1:g.9551_9552del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.482_482+1del
ENST00000295897.8:c.482_482+1del
ENST00000401494.7:c.138-550_138-549del ENSP00000384695.3:n.138-550_138-549del
ENST00000415165.6:c.138-3191_138-3190del ENSP00000401820.2:n.138-3191_138-3190del
ENST00000441319.5:c.488_488+1del
ENST00000476441.6:c.80-550_80-549del ENSP00000423727.1:n.80-550_80-549del
ENST00000503124.5:c.33-550_33-549del ENSP00000421027.1:n.33-550_33-549del
ENST00000505649.5:n.168_168+1del
ENST00000509063.5:c.482_482+1del
ENST00000510166.5:n.518_519del
ENST00000514786.1:n.451_451+1del
ENST00000515133.5:n.523_524del
ENST00000621085.4:c.482_482+1del
ENST00000621628.4:c.482_482+1del
NM_000477.5:c.482_482+1del
NM_000477.6:c.482_482+1del
NM_000477.7:c.482_482+1del