Canonical Allele Identifier: CA370093346

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845957C>G (hg19) ; chr7:g.152148872C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148872C>G , CM000669.2:g.152148872C>G	GRCh38
NC_000007.13:g.151845957C>G , CM000669.1:g.151845957C>G	GRCh37
NC_000007.12:g.151476890C>G	NCBI36
NG_033948.1:g.292134G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1243G>C
ENST00000682116.1:n.2187G>C
ENST00000682283.1:c.13226G>C	ENSP00000507485.1:p.Trp4409Ser
ENST00000682629.1:n.2355G>C
ENST00000683120.1:n.8247G>C
ENST00000683178.1:c.3628G>C
ENST00000683200.1:c.10565G>C	ENSP00000508052.1:p.Trp3522Ser
ENST00000683337.1:n.4685G>C
ENST00000683502.1:c.3700G>C
ENST00000683621.1:n.1821G>C
ENST00000683640.1:n.1771G>C
ENST00000684069.1:c.1472G>C	ENSP00000507650.1:p.Trp491Ser
ENST00000684261.1:c.7952G>C	ENSP00000508097.1:p.Trp2651Ser
ENST00000684649.1:c.3700G>C
ENST00000262189.11:c.13055G>C MANE Select	ENSP00000262189.6:p.Trp4352Ser
ENST00000360104.8:c.8842G>C
ENST00000418061.2:c.3697G>C
ENST00000424877.6:c.3631G>C
ENST00000679393.1:n.7766G>C
ENST00000679560.1:c.7955G>C	ENSP00000505094.1:p.Trp2652Ser
ENST00000679882.1:c.12620G>C	ENSP00000506154.1:p.Trp4207Ser
ENST00000680029.1:c.3632G>C
ENST00000680877.1:c.7955G>C	ENSP00000505724.1:p.Trp2652Ser
ENST00000681923.1:n.2070G>C
ENST00000262189.10:c.13055G>C	ENSP00000262189.6:p.Trp4352Ser
ENST00000355193.6:c.13055G>C	ENSP00000347325.3:p.Trp4352Ser
ENST00000360104.7:c.5736G>C
ENST00000424877.5:c.2906G>C	ENSP00000410411.1:p.Trp969Ser
ENST00000473186.5:n.10937G>C
ENST00000558084.5:c.*10575G>C	ENSP00000453752.1:n.*10575G>C
NM_170606.2:c.13055G>C	NP_733751.2:p.Trp4352Ser
XM_005250025.3:c.13271G>C	XP_005250082.1:p.Trp4424Ser
XM_005250026.2:c.13268G>C	XP_005250083.1:p.Trp4423Ser
XM_005250027.3:c.13268G>C	XP_005250084.1:p.Trp4423Ser
XM_005250028.3:c.13271G>C	XP_005250085.1:p.Trp4424Ser
XM_005250031.3:c.13106G>C	XP_005250088.1:p.Trp4369Ser
XM_006716077.2:c.13268G>C	XP_006716140.1:p.Trp4423Ser
XM_006716078.2:c.13199G>C	XP_006716141.1:p.Trp4400Ser
XM_006716079.2:c.13103G>C	XP_006716142.1:p.Trp4368Ser
XM_011516450.1:c.13223G>C	XP_011514752.1:p.Trp4408Ser
XM_011516451.1:c.13151G>C	XP_011514753.1:p.Trp4384Ser
XM_011516452.1:c.13118G>C	XP_011514754.1:p.Trp4373Ser
XM_011516453.1:c.13034G>C	XP_011514755.1:p.Trp4345Ser
XM_011516454.1:c.12356G>C	XP_011514756.1:p.Trp4119Ser
XM_011516455.1:c.10817G>C	XP_011514757.1:p.Trp3606Ser
XM_011516456.1:c.13223G>C	XP_011514758.1:p.Trp4408Ser
XM_005250025.4:c.13271G>C	XP_005250082.1:p.Trp4424Ser
XM_005250026.3:c.13268G>C	XP_005250083.1:p.Trp4423Ser
XM_005250027.4:c.13268G>C	XP_005250084.1:p.Trp4423Ser
XM_005250028.4:c.13271G>C	XP_005250085.1:p.Trp4424Ser
XM_005250031.4:c.13106G>C	XP_005250088.1:p.Trp4369Ser
XM_006716077.3:c.13268G>C	XP_006716140.1:p.Trp4423Ser
XM_006716078.3:c.13199G>C	XP_006716141.1:p.Trp4400Ser
XM_006716079.3:c.13103G>C	XP_006716142.1:p.Trp4368Ser
XM_011516450.2:c.13223G>C	XP_011514752.1:p.Trp4408Ser
XM_011516451.2:c.13151G>C	XP_011514753.1:p.Trp4384Ser
XM_011516452.2:c.13118G>C	XP_011514754.1:p.Trp4373Ser
XM_011516453.2:c.13034G>C	XP_011514755.1:p.Trp4345Ser
XM_011516454.2:c.12356G>C	XP_011514756.1:p.Trp4119Ser
XM_011516456.2:c.13223G>C	XP_011514758.1:p.Trp4408Ser
XM_017012480.1:c.13271G>C	XP_016867969.1:p.Trp4424Ser
XM_017012481.1:c.13268G>C	XP_016867970.1:p.Trp4423Ser
XM_017012482.1:c.13268G>C	XP_016867971.1:p.Trp4423Ser
XM_017012483.1:c.13268G>C	XP_016867972.1:p.Trp4423Ser
XM_017012484.1:c.13238G>C	XP_016867973.1:p.Trp4413Ser
XM_017012485.1:c.13220G>C	XP_016867974.1:p.Trp4407Ser
XM_017012486.1:c.13196G>C	XP_016867975.1:p.Trp4399Ser
XM_017012487.1:c.13124G>C	XP_016867976.1:p.Trp4375Ser
XM_017012488.1:c.13088G>C	XP_016867977.1:p.Trp4363Ser
XM_017012489.1:c.9941G>C	XP_016867978.1:p.Trp3314Ser
XM_017012490.2:c.9545G>C	XP_016867979.1:p.Trp3182Ser
XM_024446852.1:c.13268G>C	XP_024302620.1:p.Trp4423Ser
XM_024446853.1:c.13196G>C	XP_024302621.1:p.Trp4399Ser
NM_170606.3:c.13055G>C MANE Select	NP_733751.2:p.Trp4352Ser