Canonical Allele Identifier: CA370092892

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845825G>C (hg19) ; chr7:g.152148740G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148740G>C , CM000669.2:g.152148740G>C	GRCh38
NC_000007.13:g.151845825G>C , CM000669.1:g.151845825G>C	GRCh37
NC_000007.12:g.151476758G>C	NCBI36
NG_033948.1:g.292266C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1375C>G
ENST00000682116.1:n.2319C>G
ENST00000682283.1:c.13358C>G	ENSP00000507485.1:p.Pro4453Arg
ENST00000682629.1:n.2487C>G
ENST00000683120.1:n.8379C>G
ENST00000683178.1:c.3760C>G
ENST00000683200.1:c.10697C>G	ENSP00000508052.1:p.Pro3566Arg
ENST00000683337.1:n.4817C>G
ENST00000683502.1:c.3832C>G
ENST00000683621.1:n.1953C>G
ENST00000683640.1:n.1903C>G
ENST00000684069.1:c.1604C>G	ENSP00000507650.1:p.Pro535Arg
ENST00000684261.1:c.8084C>G	ENSP00000508097.1:p.Pro2695Arg
ENST00000684649.1:c.3832C>G
ENST00000262189.11:c.13187C>G MANE Select	ENSP00000262189.6:p.Pro4396Arg
ENST00000360104.8:c.8974C>G
ENST00000418061.2:c.3829C>G
ENST00000424877.6:c.3763C>G
ENST00000679393.1:n.7898C>G
ENST00000679560.1:c.8087C>G	ENSP00000505094.1:p.Pro2696Arg
ENST00000679882.1:c.12752C>G	ENSP00000506154.1:p.Pro4251Arg
ENST00000680029.1:c.3764C>G
ENST00000680877.1:c.8087C>G	ENSP00000505724.1:p.Pro2696Arg
ENST00000681923.1:n.2202C>G
ENST00000262189.10:c.13187C>G	ENSP00000262189.6:p.Pro4396Arg
ENST00000355193.6:c.13187C>G	ENSP00000347325.3:p.Pro4396Arg
ENST00000360104.7:c.5868C>G
ENST00000424877.5:c.3038C>G	ENSP00000410411.1:p.Pro1013Arg
ENST00000473186.5:n.11069C>G
ENST00000558084.5:c.*10707C>G	ENSP00000453752.1:n.*10707C>G
NM_170606.2:c.13187C>G	NP_733751.2:p.Pro4396Arg
XM_005250025.3:c.13403C>G	XP_005250082.1:p.Pro4468Arg
XM_005250026.2:c.13400C>G	XP_005250083.1:p.Pro4467Arg
XM_005250027.3:c.13400C>G	XP_005250084.1:p.Pro4467Arg
XM_005250028.3:c.13403C>G	XP_005250085.1:p.Pro4468Arg
XM_005250031.3:c.13238C>G	XP_005250088.1:p.Pro4413Arg
XM_006716077.2:c.13400C>G	XP_006716140.1:p.Pro4467Arg
XM_006716078.2:c.13331C>G	XP_006716141.1:p.Pro4444Arg
XM_006716079.2:c.13235C>G	XP_006716142.1:p.Pro4412Arg
XM_011516450.1:c.13355C>G	XP_011514752.1:p.Pro4452Arg
XM_011516451.1:c.13283C>G	XP_011514753.1:p.Pro4428Arg
XM_011516452.1:c.13250C>G	XP_011514754.1:p.Pro4417Arg
XM_011516453.1:c.13166C>G	XP_011514755.1:p.Pro4389Arg
XM_011516454.1:c.12488C>G	XP_011514756.1:p.Pro4163Arg
XM_011516455.1:c.10949C>G	XP_011514757.1:p.Pro3650Arg
XM_011516456.1:c.13355C>G	XP_011514758.1:p.Pro4452Arg
XM_005250025.4:c.13403C>G	XP_005250082.1:p.Pro4468Arg
XM_005250026.3:c.13400C>G	XP_005250083.1:p.Pro4467Arg
XM_005250027.4:c.13400C>G	XP_005250084.1:p.Pro4467Arg
XM_005250028.4:c.13403C>G	XP_005250085.1:p.Pro4468Arg
XM_005250031.4:c.13238C>G	XP_005250088.1:p.Pro4413Arg
XM_006716077.3:c.13400C>G	XP_006716140.1:p.Pro4467Arg
XM_006716078.3:c.13331C>G	XP_006716141.1:p.Pro4444Arg
XM_006716079.3:c.13235C>G	XP_006716142.1:p.Pro4412Arg
XM_011516450.2:c.13355C>G	XP_011514752.1:p.Pro4452Arg
XM_011516451.2:c.13283C>G	XP_011514753.1:p.Pro4428Arg
XM_011516452.2:c.13250C>G	XP_011514754.1:p.Pro4417Arg
XM_011516453.2:c.13166C>G	XP_011514755.1:p.Pro4389Arg
XM_011516454.2:c.12488C>G	XP_011514756.1:p.Pro4163Arg
XM_011516456.2:c.13355C>G	XP_011514758.1:p.Pro4452Arg
XM_017012480.1:c.13403C>G	XP_016867969.1:p.Pro4468Arg
XM_017012481.1:c.13400C>G	XP_016867970.1:p.Pro4467Arg
XM_017012482.1:c.13400C>G	XP_016867971.1:p.Pro4467Arg
XM_017012483.1:c.13400C>G	XP_016867972.1:p.Pro4467Arg
XM_017012484.1:c.13370C>G	XP_016867973.1:p.Pro4457Arg
XM_017012485.1:c.13352C>G	XP_016867974.1:p.Pro4451Arg
XM_017012486.1:c.13328C>G	XP_016867975.1:p.Pro4443Arg
XM_017012487.1:c.13256C>G	XP_016867976.1:p.Pro4419Arg
XM_017012488.1:c.13220C>G	XP_016867977.1:p.Pro4407Arg
XM_017012489.1:c.10073C>G	XP_016867978.1:p.Pro3358Arg
XM_017012490.2:c.9677C>G	XP_016867979.1:p.Pro3226Arg
XM_024446852.1:c.13400C>G	XP_024302620.1:p.Pro4467Arg
XM_024446853.1:c.13328C>G	XP_024302621.1:p.Pro4443Arg
NM_170606.3:c.13187C>G MANE Select	NP_733751.2:p.Pro4396Arg