Canonical Allele Identifier: CA2447976671

Gene: PCDH19

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.100407296C= , CM000685.2:g.100407296C=	GRCh38
NC_000023.10:g.99662294C= , CM000685.1:g.99662294C=	GRCh37
NC_000023.9:g.99548950C=	NCBI36
NG_021319.1:g.7978G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255531.8:c.1302G=	ENSP00000255531.7:p.Gln434=
ENST00000373034.8:c.1302G= MANE Select	ENSP00000362125.4:p.Gln434=
ENST00000420881.6:c.1302G=	ENSP00000400327.2:p.Gln434=
NM_001105243.1:c.1302G=	NP_001098713.1:p.Gln434=
NM_001184880.1:c.1302G=	NP_001171809.1:p.Gln434=
NM_020766.2:c.1302G=	NP_065817.2:p.Gln434=
XM_011530997.1:c.1302G=	XP_011529299.1:p.Gln434=
XM_011530997.2:c.1302G=	XP_011529299.1:p.Gln434=
NM_001105243.2:c.1302G=	NP_001098713.1:p.Gln434=
NM_001184880.2:c.1302G= MANE Select	NP_001171809.1:p.Gln434=
NM_020766.3:c.1302G=	NP_065817.2:p.Gln434=