Canonical Allele Identifier: CA700253525

Gene: PCDH9

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.67122013G>C , CM000675.2:g.67122013G>C	GRCh38
NC_000013.10:g.67696145G>C , CM000675.1:g.67696145G>C	GRCh37
NC_000013.9:g.66594146G>C	NCBI36
NG_011876.1:g.113324C>G
NG_011876.2:g.113324C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377865.7:c.3036+103392C>G MANE Select	ENSP00000367096.2:n.3036+103392C>G
ENST00000377865.6:c.3036+103392C>G	ENSP00000367096.2:n.3036+103392C>G
ENST00000456367.5:c.3036+103392C>G	ENSP00000401699.2:n.3036+103392C>G
ENST00000544246.5:c.3036+103392C>G	ENSP00000442186.2:n.3036+103392C>G
NM_020403.4:c.3036+103392C>G	NP_065136.1:n.3036+103392C>G
NM_203487.2:c.3036+103392C>G	NP_982354.1:n.3036+103392C>G
XM_005266406.1:c.3036+103392C>G	XP_005266463.1:n.3036+103392C>G
XM_005266407.1:c.3036+103392C>G	XP_005266464.1:n.3036+103392C>G
NM_001318372.1:c.3036+103392C>G	NP_001305301.1:n.3036+103392C>G
NM_001318373.1:c.3036+103392C>G	NP_001305302.1:n.3036+103392C>G
XM_017020619.2:c.3036+103392C>G	XP_016876108.1:n.3036+103392C>G
XM_017020620.2:c.3036+103392C>G	XP_016876109.1:n.3036+103392C>G
NM_203487.3:c.3036+103392C>G MANE Select	NP_982354.1:n.3036+103392C>G
NM_001318372.2:c.3036+103392C>G	NP_001305301.1:n.3036+103392C>G
NM_001318373.2:c.3036+103392C>G	NP_001305302.1:n.3036+103392C>G
NM_020403.5:c.3036+103392C>G	NP_065136.1:n.3036+103392C>G