Canonical Allele Identifier: CA188707961
Community Standard Title: NM_015061.6(KDM4C):c.2260-3407C>G
Gene: KDM4C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.7043455C>G , CM000671.2:g.7043455C>G GRCh38
NC_000009.11:g.7043455C>G , CM000671.1:g.7043455C>G GRCh37
NC_000009.10:g.7033455C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_015061.6:c.2260-3407C>G MANE Select NP_055876.2:n.2260-3407C>G
ENST00000381309.8:c.2260-3407C>G MANE Select ENSP00000370710.3:n.2260-3407C>G
NM_001146695.1:c.2260-3407C>G NP_001140167.1:n.2260-3407C>G
NM_001146695.2:c.2260-3407C>G NP_001140167.1:n.2260-3407C>G
NM_001146695.4:c.2260-3407C>G NP_001140167.1:n.2260-3407C>G
NM_001146696.1:c.2326-3407C>G NP_001140168.1:n.2326-3407C>G
NM_001146696.2:c.2326-3407C>G NP_001140168.1:n.2326-3407C>G
NM_001304339.1:c.2260-3407C>G NP_001291268.1:n.2260-3407C>G
NM_001304339.2:c.2260-3407C>G NP_001291268.1:n.2260-3407C>G
NM_001304339.4:c.2260-3407C>G NP_001291268.1:n.2260-3407C>G
NM_001304340.1:c.1495-3407C>G NP_001291269.1:n.1495-3407C>G
NM_001304340.2:c.1495-3407C>G NP_001291269.1:n.1495-3407C>G
NM_001304340.4:c.1495-3407C>G NP_001291269.1:n.1495-3407C>G
NM_001353997.1:c.2260-3407C>G NP_001340926.1:n.2260-3407C>G
NM_001353997.3:c.2260-3407C>G NP_001340926.1:n.2260-3407C>G
NM_001353998.1:c.2260-3407C>G NP_001340927.1:n.2260-3407C>G
NM_001353998.3:c.2260-3407C>G NP_001340927.1:n.2260-3407C>G
NM_001353999.1:c.949-3407C>G NP_001340928.1:n.949-3407C>G
NM_001353999.3:c.949-3407C>G NP_001340928.1:n.949-3407C>G
NM_001354000.1:c.949-3407C>G NP_001340929.1:n.949-3407C>G
NM_001354000.3:c.949-3407C>G NP_001340929.1:n.949-3407C>G
NM_001354001.1:c.949-3407C>G NP_001340930.1:n.949-3407C>G
NM_001354001.3:c.949-3407C>G NP_001340930.1:n.949-3407C>G
NM_015061.3:c.2260-3407C>G NP_055876.2:n.2260-3407C>G
NM_015061.4:c.2260-3407C>G NP_055876.2:n.2260-3407C>G
NR_148677.1:n.3131-3407C>G
NR_148677.3:n.2508-3407C>G
NR_148678.1:n.3131-3407C>G
NR_148678.3:n.2508-3407C>G
NR_148679.1:n.4051-3407C>G
NR_148679.3:n.3428-3407C>G
NR_148680.1:n.4055-3407C>G
NR_148680.3:n.3432-3407C>G
ENST00000381306.7:c.2260-3407C>G ENSP00000370707.3:n.2260-3407C>G
ENST00000381309.7:c.2260-3407C>G ENSP00000370710.3:n.2260-3407C>G
ENST00000420847.2:c.292-3407C>G ENSP00000400127.1:n.292-3407C>G
ENST00000428870.6:c.1321-3407C>G ENSP00000405739.2:n.1321-3407C>G
ENST00000535193.3:c.2326-3407C>G ENSP00000442382.1:n.2326-3407C>G
ENST00000536108.5:c.2260-3407C>G ENSP00000440656.2:n.2260-3407C>G
ENST00000536108.6:c.2326-3407C>G ENSP00000440656.3:n.2326-3407C>G
ENST00000543771.5:c.2260-3407C>G ENSP00000445427.1:n.2260-3407C>G
XM_006716741.1:c.2260-3407C>G XP_006716804.1:n.2260-3407C>G
XM_011517808.1:c.2260-3407C>G XP_011516110.1:n.2260-3407C>G
XM_011517809.1:c.2260-3407C>G XP_011516111.1:n.2260-3407C>G
XM_011517810.1:c.1717-3407C>G XP_011516112.1:n.1717-3407C>G
XM_011517811.1:c.1717-3407C>G XP_011516113.1:n.1717-3407C>G
XM_011517811.3:c.1717-3407C>G XP_011516113.1:n.1717-3407C>G
XM_011517812.1:c.1666-3407C>G XP_011516114.1:n.1666-3407C>G
XM_011517814.1:c.1531-3407C>G XP_011516116.1:n.1531-3407C>G
XM_011517815.1:c.*29+2599C>G XP_011516117.1:n.*29+2599C>G
XM_011517816.1:c.1321-3407C>G XP_011516118.1:n.1321-3407C>G
XM_017014498.2:c.2260-3407C>G XP_016869987.1:n.2260-3407C>G
XM_017014499.2:c.1840-3407C>G XP_016869988.1:n.1840-3407C>G
XM_017014501.2:c.1666-3407C>G XP_016869990.1:n.1666-3407C>G
XM_017014502.2:c.2260-3407C>G XP_016869991.1:n.2260-3407C>G
XM_024447458.1:c.1840-3407C>G XP_024303226.1:n.1840-3407C>G
XM_024447459.1:c.949-3407C>G XP_024303227.1:n.949-3407C>G
XR_001746252.2:n.2837-3407C>G
XR_001746255.2:n.2837-3407C>G
XR_929221.1:n.2277-3407C>G
XR_929222.1:n.2277-3407C>G
XR_929223.1:n.2277-3407C>G