Canonical Allele Identifier: CA1910754678

Gene: PCDH15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806167_53806170delinsACTT , CM000672.2:g.53806167_53806170delinsACTT	GRCh38
NC_000010.10:g.55565927_55565930delinsACTT , CM000672.1:g.55565927_55565930delinsACTT	GRCh37
NC_000010.9:g.55235933_55235936delinsACTT	NCBI36
NG_009191.2:g.1000122_1000125delinsAAGT
NG_009191.3:g.1828013_1828016delinsAAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644397.2:c.*409_*412delinsAAGT MANE Select	ENSP00000495195.1:n.*409_*412delinsAAGT
ENST00000373965.6:c.*409_*412delinsAAGT	ENSP00000363076.3:n.*409_*412delinsAAGT
ENST00000414778.5:c.*409_*412delinsAAGT	ENSP00000410304.2:n.*409_*412delinsAAGT
ENST00000614895.4:c.*409_*412delinsAAGT	ENSP00000478512.1:n.*409_*412delinsAAGT
ENST00000616114.4:c.*409_*412delinsAAGT	ENSP00000483745.1:n.*409_*412delinsAAGT
NM_001142771.1:c.*409_*412delinsAAGT	NP_001136243.1:n.*409_*412delinsAAGT
NM_001142772.1:c.*409_*412delinsAAGT	NP_001136244.1:n.*409_*412delinsAAGT
NM_001354420.1:c.*409_*412delinsAAGT	NP_001341349.1:n.*409_*412delinsAAGT
NM_001354429.1:c.*409_*412delinsAAGT	NP_001341358.1:n.*409_*412delinsAAGT
XR_001747192.2:n.11924_11927delinsAAGT
XR_001747193.2:n.11915_11918delinsAAGT
NM_001142771.2:c.*409_*412delinsAAGT	NP_001136243.1:n.*409_*412delinsAAGT
NM_001142772.2:c.*409_*412delinsAAGT	NP_001136244.1:n.*409_*412delinsAAGT
NM_001354420.2:c.*409_*412delinsAAGT	NP_001341349.1:n.*409_*412delinsAAGT
NM_001354429.2:c.*409_*412delinsAAGT	NP_001341358.1:n.*409_*412delinsAAGT
NM_001384140.1:c.*409_*412delinsAAGT MANE Select	NP_001371069.1:n.*409_*412delinsAAGT