Canonical Allele Identifier: CA1306599533
Gene: PTCHD3P2 HGNC NCBI
KLHL23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169767621A= , CM000664.2:g.169767621A= GRCh38
NC_000002.11:g.170624131A= , CM000664.1:g.170624131A= GRCh37
NC_000002.10:g.170332377A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000424937.1:n.1087+92T= (PTCHD3P2)
ENST00000437875.1:c.830-5699A= (KLHL23) ENSP00000394732.1:n.830-5699A=
ENST00000448589.1:c.46-8820A= (KLHL23)