Canonical Allele Identifier: CA517696703

Gene: PCDH19

Linked Data

• MyVariant Identifiers: chrX:g.99596947C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.100341949C>G , CM000685.2:g.100341949C>G	GRCh38
NC_000023.10:g.99596947C>G , CM000685.1:g.99596947C>G	GRCh37
NC_000023.9:g.99483603C>G	NCBI36
NG_021319.1:g.73325G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255531.8:c.2661G>C	ENSP00000255531.7:p.Val887=
ENST00000373034.8:c.2802G>C MANE Select	ENSP00000362125.4:p.Val934=
ENST00000420881.6:c.2658G>C	ENSP00000400327.2:p.Val886=
NM_001105243.1:c.2661G>C	NP_001098713.1:p.Val887=
NM_001184880.1:c.2802G>C	NP_001171809.1:p.Val934=
NM_020766.2:c.2658G>C	NP_065817.2:p.Val886=
XM_011530997.1:c.2799G>C	XP_011529299.1:p.Val933=
XM_011530997.2:c.2799G>C	XP_011529299.1:p.Val933=
NM_001105243.2:c.2661G>C	NP_001098713.1:p.Val887=
NM_001184880.2:c.2802G>C MANE Select	NP_001171809.1:p.Val934=
NM_020766.3:c.2658G>C	NP_065817.2:p.Val886=