Canonical Allele Identifier: CA728722240

Linked Data

dbSNP Id: rs1226710256

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186453322del , CM000663.2:g.186453322del GRCh38
NC_000001.10:g.186422454del , CM000663.1:g.186422454del GRCh37
NC_000001.9:g.184689077del NCBI36
NG_009101.1:g.12789del

Transcript Alleles

HGVS Amino-acid Change
ENST00000391997.3:c.-24-3836del (PDC) MANE Select ENSP00000375855.2:n.-24-3836del
ENST00000391997.2:c.-24-3836del (PDC) ENSP00000375855.2:n.-24-3836del
NM_002597.4:c.-24-3836del (PDC) NP_002588.3:n.-24-3836del
NR_126002.1:n.441+2048del (PDC-AS1)
NM_002597.5:c.-24-3836del (PDC) MANE Select NP_002588.3:n.-24-3836del