Canonical Allele Identifier: CA793840503

Gene: PCDH7

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.30748032A>T , CM000666.2:g.30748032A>T	GRCh38
NC_000004.11:g.30749654A>T , CM000666.1:g.30749654A>T	GRCh37
NC_000004.10:g.30358752A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000511884.7:c.3174+23436A>T	ENSP00000513121.1:n.3174+23436A>T
ENST00000621961.2:c.3174+23436A>T	ENSP00000484874.2:n.3174+23436A>T
ENST00000695919.1:c.3174+23436A>T MANE Select	ENSP00000512266.1:n.3174+23436A>T
ENST00000695920.1:c.3174+23436A>T	ENSP00000512267.1:n.3174+23436A>T
ENST00000695921.1:c.3174+23436A>T	ENSP00000512268.1:n.3174+23436A>T
ENST00000695922.1:c.3174+23436A>T	ENSP00000512269.2:n.3174+23436A>T
ENST00000695923.1:n.75+23436A>T
ENST00000509759.2:c.70+23436A>T
ENST00000511884.6:c.2243+23436A>T
ENST00000621961.1:c.1117+23436A>T
NM_001173523.1:c.3174+23436A>T	NP_001166994.1:n.3174+23436A>T
NM_032457.3:c.3174+23436A>T	NP_115833.2:n.3174+23436A>T
XM_005248163.2:c.3174+23436A>T	XP_005248220.1:n.3174+23436A>T
XM_005248164.2:c.3174+23436A>T	XP_005248221.1:n.3174+23436A>T
XM_005248166.2:c.3174+23436A>T	XP_005248223.1:n.3174+23436A>T
XM_011513842.1:c.3174+23436A>T	XP_011512144.1:n.3174+23436A>T
XM_011513843.1:c.3174+23436A>T	XP_011512145.1:n.3174+23436A>T
XM_011513844.1:c.3174+23436A>T	XP_011512146.1:n.3174+23436A>T
XM_011513845.1:c.3174+23436A>T	XP_011512147.1:n.3174+23436A>T
XR_925546.1:n.3750T>A
XM_005248163.4:c.3174+23436A>T	XP_005248220.1:n.3174+23436A>T
XM_005248164.4:c.3174+23436A>T	XP_005248221.1:n.3174+23436A>T
XM_005248166.4:c.3174+23436A>T	XP_005248223.1:n.3174+23436A>T
XM_011513842.3:c.3174+23436A>T	XP_011512144.1:n.3174+23436A>T
XM_011513843.3:c.3174+23436A>T	XP_011512145.1:n.3174+23436A>T
XM_011513844.3:c.3174+23436A>T	XP_011512146.1:n.3174+23436A>T
XM_017008259.2:c.3174+23436A>T	XP_016863748.1:n.3174+23436A>T
XM_017008260.2:c.3174+23436A>T	XP_016863749.1:n.3174+23436A>T
XM_017008261.2:c.3174+23436A>T	XP_016863750.1:n.3174+23436A>T
XM_017008262.2:c.3174+23436A>T	XP_016863751.1:n.3174+23436A>T
XM_017008263.2:c.3174+23436A>T	XP_016863752.1:n.3174+23436A>T
XM_017008264.2:c.3174+23436A>T	XP_016863753.1:n.3174+23436A>T
XM_017008265.2:c.3174+23436A>T	XP_016863754.1:n.3174+23436A>T
XM_017008266.2:c.3174+23436A>T	XP_016863755.1:n.3174+23436A>T
XM_017008267.2:c.3174+23436A>T	XP_016863756.1:n.3174+23436A>T
XM_017008268.2:c.3174+23436A>T	XP_016863757.1:n.3174+23436A>T
XM_017008269.2:c.3174+23436A>T	XP_016863758.1:n.3174+23436A>T
XM_017008271.2:c.3174+23436A>T	XP_016863760.1:n.3174+23436A>T
XM_017008272.2:c.3174+23436A>T	XP_016863761.1:n.3174+23436A>T
NM_001173523.2:c.3174+23436A>T MANE Select	NP_001166994.1:n.3174+23436A>T
NM_032457.4:c.3174+23436A>T	NP_115833.2:n.3174+23436A>T