Canonical Allele Identifier: CA2695233485

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949968_43950010del , CM000685.2:g.43949968_43950010del GRCh38
NC_000023.10:g.43809214_43809256del , CM000685.1:g.43809214_43809256del GRCh37
NC_000023.9:g.43694158_43694200del NCBI36
NG_009832.1:g.28670_28712del

Transcript Alleles

HGVS Amino-acid change
ENST00000642620.1:c.195_237del (NDP) MANE Select ENSP00000495972.1:p.Glu66ArgfsTer24
ENST00000647044.1:c.195_237del (NDP) ENSP00000495811.1:p.Glu66ArgfsTer24
ENST00000378062.5:c.195_237del (NDP) ENSP00000367301.5:p.Glu66ArgfsTer24
ENST00000470584.1:n.239_281del (NDP)
NM_000266.3:c.195_237del (NDP) NP_000257.1:p.Glu66ArgfsTer24
NR_046631.1:n.237_279del (NDP-AS1)
NM_000266.4:c.195_237del (NDP) MANE Select NP_000257.1:p.Glu66ArgfsTer24