Canonical Allele Identifier: CA388357895

Gene: PCDH9

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.66304864T>C , CM000675.2:g.66304864T>C	GRCh38
NC_000013.10:g.66878996T>C , CM000675.1:g.66878996T>C	GRCh37
NC_000013.9:g.65776997T>C	NCBI36
NG_011876.1:g.930473A>G
NG_011876.2:g.930473A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_203487.3:c.3505A>G MANE Select	NP_982354.1:p.Lys1169Glu
ENST00000377865.7:c.3505A>G MANE Select	ENSP00000367096.2:p.Lys1169Glu
NM_001318372.1:c.3379A>G	NP_001305301.1:p.Lys1127Glu
NM_001318372.2:c.3379A>G	NP_001305301.1:p.Lys1127Glu
NM_001318373.1:c.3277A>G	NP_001305302.1:p.Lys1093Glu
NM_001318373.2:c.3277A>G	NP_001305302.1:p.Lys1093Glu
NM_020403.4:c.3403A>G	NP_065136.1:p.Lys1135Glu
NM_020403.5:c.3403A>G	NP_065136.1:p.Lys1135Glu
NM_203487.2:c.3505A>G	NP_982354.1:p.Lys1169Glu
ENST00000377865.6:c.3505A>G	ENSP00000367096.2:p.Lys1169Glu
ENST00000456367.5:c.3379A>G	ENSP00000401699.2:p.Lys1127Glu
ENST00000544246.5:c.3403A>G	ENSP00000442186.2:p.Lys1135Glu
ENST00000617020.1:n.299A>G
XM_005266406.1:c.3379A>G	XP_005266463.1:p.Lys1127Glu
XM_005266407.1:c.3277A>G	XP_005266464.1:p.Lys1093Glu
XM_017020619.2:c.3505A>G	XP_016876108.1:p.Lys1169Glu