Canonical Allele Identifier: CA2694250643

Gene: PCDH19

Linked Data

• gnomAD v4: X-100341760-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.100341765del , CM000685.2:g.100341765del	GRCh38
NC_000023.10:g.99596763del , CM000685.1:g.99596763del	GRCh37
NC_000023.9:g.99483419del	NCBI36
NG_021319.1:g.73513del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255531.8:c.2707+142del	ENSP00000255531.7:n.2707+142del
ENST00000373034.8:c.2848+142del MANE Select	ENSP00000362125.4:n.2848+142del
ENST00000420881.6:c.2704+142del	ENSP00000400327.2:n.2704+142del
NM_001105243.1:c.2707+142del	NP_001098713.1:n.2707+142del
NM_001184880.1:c.2848+142del	NP_001171809.1:n.2848+142del
NM_020766.2:c.2704+142del	NP_065817.2:n.2704+142del
XM_011530997.1:c.2845+142del	XP_011529299.1:n.2845+142del
XM_011530997.2:c.2845+142del	XP_011529299.1:n.2845+142del
NM_001105243.2:c.2707+142del	NP_001098713.1:n.2707+142del
NM_001184880.2:c.2848+142del MANE Select	NP_001171809.1:n.2848+142del
NM_020766.3:c.2704+142del	NP_065817.2:n.2704+142del