Canonical Allele Identifier: CA593495460

Gene: PCDH15

Linked Data

• gnomAD v2: 10-55565947-G-GTTTTTT
• gnomAD v3: 10-53806187-G-GTTTTTT
• gnomAD v4: 10-53806187-G-GTTTTTT
• MyVariant Identifiers: chr10:g.55565947_55565948insTTTTTT (hg19) ; chr10:g.53806187_53806188insTTTTTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806187_53806188insTTTTTT , CM000672.2:g.53806187_53806188insTTTTTT	GRCh38
NC_000010.10:g.55565947_55565948insTTTTTT , CM000672.1:g.55565947_55565948insTTTTTT	GRCh37
NC_000010.9:g.55235953_55235954insTTTTTT	NCBI36
NG_009191.2:g.1000104_1000105insAAAAAA
NG_009191.3:g.1827995_1827996insAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644397.2:c.*391_*392insAAAAAA MANE Select	ENSP00000495195.1:n.*391_*392insAAAAAA
ENST00000373965.6:c.*391_*392insAAAAAA	ENSP00000363076.3:n.*391_*392insAAAAAA
ENST00000414778.5:c.*391_*392insAAAAAA	ENSP00000410304.2:n.*391_*392insAAAAAA
ENST00000614895.4:c.*391_*392insAAAAAA	ENSP00000478512.1:n.*391_*392insAAAAAA
ENST00000616114.4:c.*391_*392insAAAAAA	ENSP00000483745.1:n.*391_*392insAAAAAA
NM_001142771.1:c.*391_*392insAAAAAA	NP_001136243.1:n.*391_*392insAAAAAA
NM_001142772.1:c.*391_*392insAAAAAA	NP_001136244.1:n.*391_*392insAAAAAA
NM_001354420.1:c.*391_*392insAAAAAA	NP_001341349.1:n.*391_*392insAAAAAA
NM_001354429.1:c.*391_*392insAAAAAA	NP_001341358.1:n.*391_*392insAAAAAA
XR_001747192.2:n.11906_11907insAAAAAA
XR_001747193.2:n.11897_11898insAAAAAA
NM_001142771.2:c.*391_*392insAAAAAA	NP_001136243.1:n.*391_*392insAAAAAA
NM_001142772.2:c.*391_*392insAAAAAA	NP_001136244.1:n.*391_*392insAAAAAA
NM_001354420.2:c.*391_*392insAAAAAA	NP_001341349.1:n.*391_*392insAAAAAA
NM_001354429.2:c.*391_*392insAAAAAA	NP_001341358.1:n.*391_*392insAAAAAA
NM_001384140.1:c.*391_*392insAAAAAA MANE Select	NP_001371069.1:n.*391_*392insAAAAAA