Canonical Allele Identifier: CA13130334

Gene: KDM4C

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6977633G>A , CM000671.2:g.6977633G>A	GRCh38
NC_000009.11:g.6977633G>A , CM000671.1:g.6977633G>A	GRCh37
NC_000009.10:g.6967633G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536108.6:c.988-3292G>A	ENSP00000440656.3:n.988-3292G>A
ENST00000381309.8:c.922-3292G>A MANE Select	ENSP00000370710.3:n.922-3292G>A
ENST00000381306.7:c.922-3292G>A	ENSP00000370707.3:n.922-3292G>A
ENST00000381309.7:c.922-3292G>A	ENSP00000370710.3:n.922-3292G>A
ENST00000428870.6:c.-18-3292G>A	ENSP00000405739.2:n.-18-3292G>A
ENST00000438023.5:c.922-3292G>A	ENSP00000404756.1:n.922-3292G>A
ENST00000535193.3:c.988-3292G>A	ENSP00000442382.1:n.988-3292G>A
ENST00000536108.5:c.922-3292G>A	ENSP00000440656.2:n.922-3292G>A
ENST00000543771.5:c.922-3292G>A	ENSP00000445427.1:n.922-3292G>A
NM_001146695.1:c.922-3292G>A	NP_001140167.1:n.922-3292G>A
NM_001146696.1:c.988-3292G>A	NP_001140168.1:n.988-3292G>A
NM_001304339.1:c.922-3292G>A	NP_001291268.1:n.922-3292G>A
NM_001304340.1:c.379-3292G>A	NP_001291269.1:n.379-3292G>A
NM_015061.3:c.922-3292G>A	NP_055876.2:n.922-3292G>A
NR_130707.1:n.1502-3292G>A
XM_006716741.1:c.922-3292G>A	XP_006716804.1:n.922-3292G>A
XM_011517808.1:c.922-3292G>A	XP_011516110.1:n.922-3292G>A
XM_011517809.1:c.922-3292G>A	XP_011516111.1:n.922-3292G>A
XM_011517810.1:c.379-3292G>A	XP_011516112.1:n.379-3292G>A
XM_011517811.1:c.379-3292G>A	XP_011516113.1:n.379-3292G>A
XM_011517812.1:c.328-3292G>A	XP_011516114.1:n.328-3292G>A
XM_011517814.1:c.193-3292G>A	XP_011516116.1:n.193-3292G>A
XM_011517815.1:c.922-3292G>A	XP_011516117.1:n.922-3292G>A
XM_011517816.1:c.-19+2694G>A	XP_011516118.1:n.-19+2694G>A
XR_929221.1:n.939-3292G>A
XR_929222.1:n.939-3292G>A
XR_929223.1:n.939-3292G>A
NM_001146695.2:c.922-3292G>A	NP_001140167.1:n.922-3292G>A
NM_001304339.2:c.922-3292G>A	NP_001291268.1:n.922-3292G>A
NM_001304340.2:c.379-3292G>A	NP_001291269.1:n.379-3292G>A
NM_001353997.1:c.922-3292G>A	NP_001340926.1:n.922-3292G>A
NM_001353998.1:c.922-3292G>A	NP_001340927.1:n.922-3292G>A
NM_001353999.1:c.-1314-3292G>A	NP_001340928.1:n.-1314-3292G>A
NM_001354000.1:c.-527-3292G>A	NP_001340929.1:n.-527-3292G>A
NM_001354001.1:c.-1314-3292G>A	NP_001340930.1:n.-1314-3292G>A
NM_015061.4:c.922-3292G>A	NP_055876.2:n.922-3292G>A
NR_130707.2:n.1793-3292G>A
NR_148677.1:n.1793-3292G>A
NR_148678.1:n.1793-3292G>A
NR_148679.1:n.1793-3292G>A
NR_148680.1:n.1793-3292G>A
XM_011517811.3:c.379-3292G>A	XP_011516113.1:n.379-3292G>A
XM_017014498.2:c.922-3292G>A	XP_016869987.1:n.922-3292G>A
XM_017014499.2:c.502-3292G>A	XP_016869988.1:n.502-3292G>A
XM_017014501.2:c.328-3292G>A	XP_016869990.1:n.328-3292G>A
XM_017014502.2:c.922-3292G>A	XP_016869991.1:n.922-3292G>A
XM_017014504.2:c.922-3292G>A	XP_016869993.1:n.922-3292G>A
XM_024447458.1:c.502-3292G>A	XP_024303226.1:n.502-3292G>A
XM_024447459.1:c.-2037-3292G>A	XP_024303227.1:n.-2037-3292G>A
XR_001746252.2:n.1499-3292G>A
XR_001746255.2:n.1499-3292G>A
NM_001146695.4:c.922-3292G>A	NP_001140167.1:n.922-3292G>A
NM_001146696.2:c.988-3292G>A	NP_001140168.1:n.988-3292G>A
NM_001304339.4:c.922-3292G>A	NP_001291268.1:n.922-3292G>A
NM_001304340.4:c.379-3292G>A	NP_001291269.1:n.379-3292G>A
NM_001353997.3:c.922-3292G>A	NP_001340926.1:n.922-3292G>A
NM_001353998.3:c.922-3292G>A	NP_001340927.1:n.922-3292G>A
NM_001353999.3:c.-1314-3292G>A	NP_001340928.1:n.-1314-3292G>A
NM_001354000.3:c.-527-3292G>A	NP_001340929.1:n.-527-3292G>A
NM_001354001.3:c.-1314-3292G>A	NP_001340930.1:n.-1314-3292G>A
NM_015061.6:c.922-3292G>A MANE Select	NP_055876.2:n.922-3292G>A
NR_130707.4:n.1170-3292G>A
NR_148677.3:n.1170-3292G>A
NR_148678.3:n.1170-3292G>A
NR_148679.3:n.1170-3292G>A
NR_148680.3:n.1170-3292G>A