Canonical Allele Identifier: CA653310627
Gene: PCDH15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.53806271_53806272insC , CM000672.2:g.53806271_53806272insC GRCh38
NC_000010.10:g.55566031_55566032insC , CM000672.1:g.55566031_55566032insC GRCh37
NC_000010.9:g.55236037_55236038insC NCBI36
NG_009191.2:g.1000020_1000021insG
NG_009191.3:g.1827911_1827912insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000644397.2:c.*307_*308insG MANE Select ENSP00000495195.1:n.*307_*308insG
ENST00000373965.6:c.*307_*308insG ENSP00000363076.3:n.*307_*308insG
ENST00000414778.5:c.*307_*308insG ENSP00000410304.2:n.*307_*308insG
ENST00000614895.4:c.*307_*308insG ENSP00000478512.1:n.*307_*308insG
ENST00000616114.4:c.*307_*308insG ENSP00000483745.1:n.*307_*308insG
NM_001142771.1:c.*307_*308insG NP_001136243.1:n.*307_*308insG
NM_001142772.1:c.*307_*308insG NP_001136244.1:n.*307_*308insG
NM_001354420.1:c.*307_*308insG NP_001341349.1:n.*307_*308insG
NM_001354429.1:c.*307_*308insG NP_001341358.1:n.*307_*308insG
XR_001747192.2:n.11822_11823insG
XR_001747193.2:n.11813_11814insG
NM_001142771.2:c.*307_*308insG NP_001136243.1:n.*307_*308insG
NM_001142772.2:c.*307_*308insG NP_001136244.1:n.*307_*308insG
NM_001354420.2:c.*307_*308insG NP_001341349.1:n.*307_*308insG
NM_001354429.2:c.*307_*308insG NP_001341358.1:n.*307_*308insG
NM_001384140.1:c.*307_*308insG MANE Select NP_001371069.1:n.*307_*308insG