Canonical Allele Identifier: CA1830864237

Gene: KDM4C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.7155356A>C , CM000671.2:g.7155356A>C	GRCh38
NC_000009.11:g.7155356A>C , CM000671.1:g.7155356A>C	GRCh37
NC_000009.10:g.7145356A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381309.8:c.2782-9882A>C MANE Select	ENSP00000370710.3:n.2782-9882A>C
ENST00000381306.7:c.2782-9882A>C	ENSP00000370707.3:n.2782-9882A>C
ENST00000381309.7:c.2782-9882A>C	ENSP00000370710.3:n.2782-9882A>C
ENST00000420847.2:c.913-9882A>C	ENSP00000400127.1:n.913-9882A>C
ENST00000428870.6:c.1843-9882A>C	ENSP00000405739.2:n.1843-9882A>C
ENST00000466673.1:n.331-9882A>C
ENST00000490806.5:n.259-9882A>C
NM_001304339.1:c.2782-9882A>C	NP_001291268.1:n.2782-9882A>C
NM_001304340.1:c.2017-9882A>C	NP_001291269.1:n.2017-9882A>C
NM_015061.3:c.2782-9882A>C	NP_055876.2:n.2782-9882A>C
XM_006716741.1:c.2881-9882A>C	XP_006716804.1:n.2881-9882A>C
XM_011517808.1:c.2881-9882A>C	XP_011516110.1:n.2881-9882A>C
XM_011517809.1:c.2611-9882A>C	XP_011516111.1:n.2611-9882A>C
XM_011517810.1:c.2338-9882A>C	XP_011516112.1:n.2338-9882A>C
XM_011517811.1:c.2338-9882A>C	XP_011516113.1:n.2338-9882A>C
XM_011517812.1:c.2287-9882A>C	XP_011516114.1:n.2287-9882A>C
XM_011517814.1:c.2152-9882A>C	XP_011516116.1:n.2152-9882A>C
XM_011517816.1:c.1942-9882A>C	XP_011516118.1:n.1942-9882A>C
XR_929221.1:n.2690-9882A>C
XR_929223.1:n.2519-9882A>C
NM_001304339.2:c.2782-9882A>C	NP_001291268.1:n.2782-9882A>C
NM_001304340.2:c.2017-9882A>C	NP_001291269.1:n.2017-9882A>C
NM_001353997.1:c.2881-9882A>C	NP_001340926.1:n.2881-9882A>C
NM_001353999.1:c.1570-9882A>C	NP_001340928.1:n.1570-9882A>C
NM_001354000.1:c.1471-9882A>C	NP_001340929.1:n.1471-9882A>C
NM_001354001.1:c.1471-9882A>C	NP_001340930.1:n.1471-9882A>C
NM_015061.4:c.2782-9882A>C	NP_055876.2:n.2782-9882A>C
NR_148677.1:n.3643-9882A>C
NR_148678.1:n.3544-9882A>C
NR_148679.1:n.4563-9882A>C
NR_148680.1:n.4468-9882A>C
XM_011517811.3:c.2338-9882A>C	XP_011516113.1:n.2338-9882A>C
XM_017014498.2:c.2611-9882A>C	XP_016869987.1:n.2611-9882A>C
XM_017014499.2:c.2461-9882A>C	XP_016869988.1:n.2461-9882A>C
XM_017014501.2:c.2188-9882A>C	XP_016869990.1:n.2188-9882A>C
XM_024447458.1:c.2461-9882A>C	XP_024303226.1:n.2461-9882A>C
XM_024447459.1:c.1471-9882A>C	XP_024303227.1:n.1471-9882A>C
XR_001746252.2:n.4659-9882A>C
XR_001746255.2:n.3079-9882A>C
NM_001304339.4:c.2782-9882A>C	NP_001291268.1:n.2782-9882A>C
NM_001304340.4:c.2017-9882A>C	NP_001291269.1:n.2017-9882A>C
NM_001353997.3:c.2881-9882A>C	NP_001340926.1:n.2881-9882A>C
NM_001353999.3:c.1570-9882A>C	NP_001340928.1:n.1570-9882A>C
NM_001354000.3:c.1471-9882A>C	NP_001340929.1:n.1471-9882A>C
NM_001354001.3:c.1471-9882A>C	NP_001340930.1:n.1471-9882A>C
NM_015061.6:c.2782-9882A>C MANE Select	NP_055876.2:n.2782-9882A>C
NR_148677.3:n.3020-9882A>C
NR_148678.3:n.2921-9882A>C
NR_148679.3:n.3940-9882A>C
NR_148680.3:n.3845-9882A>C