Canonical Allele Identifier: CA2447977038
Gene: PCDH19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.100408135C= , CM000685.2:g.100408135C= GRCh38
NC_000023.10:g.99663133C= , CM000685.1:g.99663133C= GRCh37
NC_000023.9:g.99549789C= NCBI36
NG_021319.1:g.7139G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000255531.8:c.463G= ENSP00000255531.7:p.Asp155=
ENST00000373034.8:c.463G= MANE Select ENSP00000362125.4:p.Asp155=
ENST00000420881.6:c.463G= ENSP00000400327.2:p.Asp155=
NM_001105243.1:c.463G= NP_001098713.1:p.Asp155=
NM_001184880.1:c.463G= NP_001171809.1:p.Asp155=
NM_020766.2:c.463G= NP_065817.2:p.Asp155=
XM_011530997.1:c.463G= XP_011529299.1:p.Asp155=
XM_011530997.2:c.463G= XP_011529299.1:p.Asp155=
NM_001105243.2:c.463G= NP_001098713.1:p.Asp155=
NM_001184880.2:c.463G= MANE Select NP_001171809.1:p.Asp155=
NM_020766.3:c.463G= NP_065817.2:p.Asp155=