Canonical Allele Identifier: CA2447976916

Gene: PCDH19

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.100407902A= , CM000685.2:g.100407902A=	GRCh38
NC_000023.10:g.99662900A= , CM000685.1:g.99662900A=	GRCh37
NC_000023.9:g.99549556A=	NCBI36
NG_021319.1:g.7372T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255531.8:c.696T=	ENSP00000255531.7:p.Asn232=
ENST00000373034.8:c.696T= MANE Select	ENSP00000362125.4:p.Asn232=
ENST00000420881.6:c.696T=	ENSP00000400327.2:p.Asn232=
NM_001105243.1:c.696T=	NP_001098713.1:p.Asn232=
NM_001184880.1:c.696T=	NP_001171809.1:p.Asn232=
NM_020766.2:c.696T=	NP_065817.2:p.Asn232=
XM_011530997.1:c.696T=	XP_011529299.1:p.Asn232=
XM_011530997.2:c.696T=	XP_011529299.1:p.Asn232=
NM_001105243.2:c.696T=	NP_001098713.1:p.Asn232=
NM_001184880.2:c.696T= MANE Select	NP_001171809.1:p.Asn232=
NM_020766.3:c.696T=	NP_065817.2:p.Asn232=