Canonical Allele Identifier: CA370093100

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845886C>G (hg19) ; chr7:g.152148801C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148801C>G , CM000669.2:g.152148801C>G	GRCh38
NC_000007.13:g.151845886C>G , CM000669.1:g.151845886C>G	GRCh37
NC_000007.12:g.151476819C>G	NCBI36
NG_033948.1:g.292205G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1314G>C
ENST00000682116.1:n.2258G>C
ENST00000682283.1:c.13297G>C	ENSP00000507485.1:p.Glu4433Gln
ENST00000682629.1:n.2426G>C
ENST00000683120.1:n.8318G>C
ENST00000683178.1:c.3699G>C
ENST00000683200.1:c.10636G>C	ENSP00000508052.1:p.Glu3546Gln
ENST00000683337.1:n.4756G>C
ENST00000683502.1:c.3771G>C
ENST00000683621.1:n.1892G>C
ENST00000683640.1:n.1842G>C
ENST00000684069.1:c.1543G>C	ENSP00000507650.1:p.Glu515Gln
ENST00000684261.1:c.8023G>C	ENSP00000508097.1:p.Glu2675Gln
ENST00000684649.1:c.3771G>C
ENST00000262189.11:c.13126G>C MANE Select	ENSP00000262189.6:p.Glu4376Gln
ENST00000360104.8:c.8913G>C
ENST00000418061.2:c.3768G>C
ENST00000424877.6:c.3702G>C
ENST00000679393.1:n.7837G>C
ENST00000679560.1:c.8026G>C	ENSP00000505094.1:p.Glu2676Gln
ENST00000679882.1:c.12691G>C	ENSP00000506154.1:p.Glu4231Gln
ENST00000680029.1:c.3703G>C
ENST00000680877.1:c.8026G>C	ENSP00000505724.1:p.Glu2676Gln
ENST00000681923.1:n.2141G>C
ENST00000262189.10:c.13126G>C	ENSP00000262189.6:p.Glu4376Gln
ENST00000355193.6:c.13126G>C	ENSP00000347325.3:p.Glu4376Gln
ENST00000360104.7:c.5807G>C
ENST00000424877.5:c.2977G>C	ENSP00000410411.1:p.Glu993Gln
ENST00000473186.5:n.11008G>C
ENST00000558084.5:c.*10646G>C	ENSP00000453752.1:n.*10646G>C
NM_170606.2:c.13126G>C	NP_733751.2:p.Glu4376Gln
XM_005250025.3:c.13342G>C	XP_005250082.1:p.Glu4448Gln
XM_005250026.2:c.13339G>C	XP_005250083.1:p.Glu4447Gln
XM_005250027.3:c.13339G>C	XP_005250084.1:p.Glu4447Gln
XM_005250028.3:c.13342G>C	XP_005250085.1:p.Glu4448Gln
XM_005250031.3:c.13177G>C	XP_005250088.1:p.Glu4393Gln
XM_006716077.2:c.13339G>C	XP_006716140.1:p.Glu4447Gln
XM_006716078.2:c.13270G>C	XP_006716141.1:p.Glu4424Gln
XM_006716079.2:c.13174G>C	XP_006716142.1:p.Glu4392Gln
XM_011516450.1:c.13294G>C	XP_011514752.1:p.Glu4432Gln
XM_011516451.1:c.13222G>C	XP_011514753.1:p.Glu4408Gln
XM_011516452.1:c.13189G>C	XP_011514754.1:p.Glu4397Gln
XM_011516453.1:c.13105G>C	XP_011514755.1:p.Glu4369Gln
XM_011516454.1:c.12427G>C	XP_011514756.1:p.Glu4143Gln
XM_011516455.1:c.10888G>C	XP_011514757.1:p.Glu3630Gln
XM_011516456.1:c.13294G>C	XP_011514758.1:p.Glu4432Gln
XM_005250025.4:c.13342G>C	XP_005250082.1:p.Glu4448Gln
XM_005250026.3:c.13339G>C	XP_005250083.1:p.Glu4447Gln
XM_005250027.4:c.13339G>C	XP_005250084.1:p.Glu4447Gln
XM_005250028.4:c.13342G>C	XP_005250085.1:p.Glu4448Gln
XM_005250031.4:c.13177G>C	XP_005250088.1:p.Glu4393Gln
XM_006716077.3:c.13339G>C	XP_006716140.1:p.Glu4447Gln
XM_006716078.3:c.13270G>C	XP_006716141.1:p.Glu4424Gln
XM_006716079.3:c.13174G>C	XP_006716142.1:p.Glu4392Gln
XM_011516450.2:c.13294G>C	XP_011514752.1:p.Glu4432Gln
XM_011516451.2:c.13222G>C	XP_011514753.1:p.Glu4408Gln
XM_011516452.2:c.13189G>C	XP_011514754.1:p.Glu4397Gln
XM_011516453.2:c.13105G>C	XP_011514755.1:p.Glu4369Gln
XM_011516454.2:c.12427G>C	XP_011514756.1:p.Glu4143Gln
XM_011516456.2:c.13294G>C	XP_011514758.1:p.Glu4432Gln
XM_017012480.1:c.13342G>C	XP_016867969.1:p.Glu4448Gln
XM_017012481.1:c.13339G>C	XP_016867970.1:p.Glu4447Gln
XM_017012482.1:c.13339G>C	XP_016867971.1:p.Glu4447Gln
XM_017012483.1:c.13339G>C	XP_016867972.1:p.Glu4447Gln
XM_017012484.1:c.13309G>C	XP_016867973.1:p.Glu4437Gln
XM_017012485.1:c.13291G>C	XP_016867974.1:p.Glu4431Gln
XM_017012486.1:c.13267G>C	XP_016867975.1:p.Glu4423Gln
XM_017012487.1:c.13195G>C	XP_016867976.1:p.Glu4399Gln
XM_017012488.1:c.13159G>C	XP_016867977.1:p.Glu4387Gln
XM_017012489.1:c.10012G>C	XP_016867978.1:p.Glu3338Gln
XM_017012490.2:c.9616G>C	XP_016867979.1:p.Glu3206Gln
XM_024446852.1:c.13339G>C	XP_024302620.1:p.Glu4447Gln
XM_024446853.1:c.13267G>C	XP_024302621.1:p.Glu4423Gln
NM_170606.3:c.13126G>C MANE Select	NP_733751.2:p.Glu4376Gln