Canonical Allele Identifier: CA2447955680

Gene: PCDH19

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.100341973A= , CM000685.2:g.100341973A=	GRCh38
NC_000023.10:g.99596971A= , CM000685.1:g.99596971A=	GRCh37
NC_000023.9:g.99483627A=	NCBI36
NG_021319.1:g.73301T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255531.8:c.2637T=	ENSP00000255531.7:p.Tyr879=
ENST00000373034.8:c.2778T= MANE Select	ENSP00000362125.4:p.Tyr926=
ENST00000420881.6:c.2634T=	ENSP00000400327.2:p.Tyr878=
NM_001105243.1:c.2637T=	NP_001098713.1:p.Tyr879=
NM_001184880.1:c.2778T=	NP_001171809.1:p.Tyr926=
NM_020766.2:c.2634T=	NP_065817.2:p.Tyr878=
XM_011530997.1:c.2775T=	XP_011529299.1:p.Tyr925=
XM_011530997.2:c.2775T=	XP_011529299.1:p.Tyr925=
NM_001105243.2:c.2637T=	NP_001098713.1:p.Tyr879=
NM_001184880.2:c.2778T= MANE Select	NP_001171809.1:p.Tyr926=
NM_020766.3:c.2634T=	NP_065817.2:p.Tyr878=