Canonical Allele Identifier: CA2447976617
Gene: PCDH19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.100407171G= , CM000685.2:g.100407171G= GRCh38
NC_000023.10:g.99662169G= , CM000685.1:g.99662169G= GRCh37
NC_000023.9:g.99548825G= NCBI36
NG_021319.1:g.8103C=

Transcript Alleles

HGVS Amino-acid change
ENST00000255531.8:c.1427C= ENSP00000255531.7:p.Ser476=
ENST00000373034.8:c.1427C= MANE Select ENSP00000362125.4:p.Ser476=
ENST00000420881.6:c.1427C= ENSP00000400327.2:p.Ser476=
NM_001105243.1:c.1427C= NP_001098713.1:p.Ser476=
NM_001184880.1:c.1427C= NP_001171809.1:p.Ser476=
NM_020766.2:c.1427C= NP_065817.2:p.Ser476=
XM_011530997.1:c.1427C= XP_011529299.1:p.Ser476=
XM_011530997.2:c.1427C= XP_011529299.1:p.Ser476=
NM_001105243.2:c.1427C= NP_001098713.1:p.Ser476=
NM_001184880.2:c.1427C= MANE Select NP_001171809.1:p.Ser476=
NM_020766.3:c.1427C= NP_065817.2:p.Ser476=