Canonical Allele Identifier: CA413999722

Gene: PCDH19

Linked Data

• MyVariant Identifiers: chrX:g.99596907C>A (hg19) ; chrX:g.100341909C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.100341909C>A , CM000685.2:g.100341909C>A	GRCh38
NC_000023.10:g.99596907C>A , CM000685.1:g.99596907C>A	GRCh37
NC_000023.9:g.99483563C>A	NCBI36
NG_021319.1:g.73365G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255531.8:c.2701G>T	ENSP00000255531.7:p.Asp901Tyr
ENST00000373034.8:c.2842G>T MANE Select	ENSP00000362125.4:p.Asp948Tyr
ENST00000420881.6:c.2698G>T	ENSP00000400327.2:p.Asp900Tyr
NM_001105243.1:c.2701G>T	NP_001098713.1:p.Asp901Tyr
NM_001184880.1:c.2842G>T	NP_001171809.1:p.Asp948Tyr
NM_020766.2:c.2698G>T	NP_065817.2:p.Asp900Tyr
XM_011530997.1:c.2839G>T	XP_011529299.1:p.Asp947Tyr
XM_011530997.2:c.2839G>T	XP_011529299.1:p.Asp947Tyr
NM_001105243.2:c.2701G>T	NP_001098713.1:p.Asp901Tyr
NM_001184880.2:c.2842G>T MANE Select	NP_001171809.1:p.Asp948Tyr
NM_020766.3:c.2698G>T	NP_065817.2:p.Asp900Tyr