Canonical Allele Identifier: CA2447955693

Gene: PCDH19

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.100342025T= , CM000685.2:g.100342025T=	GRCh38
NC_000023.10:g.99597023T= , CM000685.1:g.99597023T=	GRCh37
NC_000023.9:g.99483679T=	NCBI36
NG_021319.1:g.73249A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255531.8:c.2585A=	ENSP00000255531.7:p.His862=
ENST00000373034.8:c.2726A= MANE Select	ENSP00000362125.4:p.His909=
ENST00000420881.6:c.2582A=	ENSP00000400327.2:p.His861=
NM_001105243.1:c.2585A=	NP_001098713.1:p.His862=
NM_001184880.1:c.2726A=	NP_001171809.1:p.His909=
NM_020766.2:c.2582A=	NP_065817.2:p.His861=
XM_011530997.1:c.2723A=	XP_011529299.1:p.His908=
XM_011530997.2:c.2723A=	XP_011529299.1:p.His908=
NM_001105243.2:c.2585A=	NP_001098713.1:p.His862=
NM_001184880.2:c.2726A= MANE Select	NP_001171809.1:p.His909=
NM_020766.3:c.2582A=	NP_065817.2:p.His861=