Canonical Allele Identifier: CA728722293

Linked Data

dbSNP Id: rs1186899955

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186453389_186453391del , CM000663.2:g.186453389_186453391del GRCh38
NC_000001.10:g.186422521_186422523del , CM000663.1:g.186422521_186422523del GRCh37
NC_000001.9:g.184689144_184689146del NCBI36
NG_009101.1:g.12719_12721del

Transcript Alleles

HGVS Amino-acid Change
ENST00000391997.3:c.-24-3906_-24-3904del (PDC) MANE Select ENSP00000375855.2:n.-24-3906_-24-3904del
ENST00000391997.2:c.-24-3906_-24-3904del (PDC) ENSP00000375855.2:n.-24-3906_-24-3904del
NM_002597.4:c.-24-3906_-24-3904del (PDC) NP_002588.3:n.-24-3906_-24-3904del
NR_126002.1:n.441+2115_441+2117del (PDC-AS1)
NM_002597.5:c.-24-3906_-24-3904del (PDC) MANE Select NP_002588.3:n.-24-3906_-24-3904del