Canonical Allele Identifier: CA2507467590

Gene: PCDH19

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.100341746del , CM000685.2:g.100341746del	GRCh38
NC_000023.10:g.99596744del , CM000685.1:g.99596744del	GRCh37
NC_000023.9:g.99483400del	NCBI36
NG_021319.1:g.73529del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255531.8:c.2707+158del	ENSP00000255531.7:n.2707+158del
ENST00000373034.8:c.2848+158del MANE Select	ENSP00000362125.4:n.2848+158del
ENST00000420881.6:c.2704+158del	ENSP00000400327.2:n.2704+158del
NM_001105243.1:c.2707+158del	NP_001098713.1:n.2707+158del
NM_001184880.1:c.2848+158del	NP_001171809.1:n.2848+158del
NM_020766.2:c.2704+158del	NP_065817.2:n.2704+158del
XM_011530997.1:c.2845+158del	XP_011529299.1:n.2845+158del
XM_011530997.2:c.2845+158del	XP_011529299.1:n.2845+158del
NM_001105243.2:c.2707+158del	NP_001098713.1:n.2707+158del
NM_001184880.2:c.2848+158del MANE Select	NP_001171809.1:n.2848+158del
NM_020766.3:c.2704+158del	NP_065817.2:n.2704+158del