Canonical Allele Identifier: CA414000022

Gene: PCDH19

Linked Data

• MyVariant Identifiers: chrX:g.99596990T>A (hg19) ; chrX:g.100341992T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.100341992T>A , CM000685.2:g.100341992T>A	GRCh38
NC_000023.10:g.99596990T>A , CM000685.1:g.99596990T>A	GRCh37
NC_000023.9:g.99483646T>A	NCBI36
NG_021319.1:g.73282A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255531.8:c.2618A>T	ENSP00000255531.7:p.Asp873Val
ENST00000373034.8:c.2759A>T MANE Select	ENSP00000362125.4:p.Asp920Val
ENST00000420881.6:c.2615A>T	ENSP00000400327.2:p.Asp872Val
NM_001105243.1:c.2618A>T	NP_001098713.1:p.Asp873Val
NM_001184880.1:c.2759A>T	NP_001171809.1:p.Asp920Val
NM_020766.2:c.2615A>T	NP_065817.2:p.Asp872Val
XM_011530997.1:c.2756A>T	XP_011529299.1:p.Asp919Val
XM_011530997.2:c.2756A>T	XP_011529299.1:p.Asp919Val
NM_001105243.2:c.2618A>T	NP_001098713.1:p.Asp873Val
NM_001184880.2:c.2759A>T MANE Select	NP_001171809.1:p.Asp920Val
NM_020766.3:c.2615A>T	NP_065817.2:p.Asp872Val