Canonical Allele Identifier: CA458884922

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845955T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148870T>G , CM000669.2:g.152148870T>G	GRCh38
NC_000007.13:g.151845955T>G , CM000669.1:g.151845955T>G	GRCh37
NC_000007.12:g.151476888T>G	NCBI36
NG_033948.1:g.292136A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1245A>C
ENST00000682116.1:n.2189A>C
ENST00000682283.1:c.13228A>C	ENSP00000507485.1:p.Arg4410=
ENST00000682629.1:n.2357A>C
ENST00000683120.1:n.8249A>C
ENST00000683178.1:c.3630A>C
ENST00000683200.1:c.10567A>C	ENSP00000508052.1:p.Arg3523=
ENST00000683337.1:n.4687A>C
ENST00000683502.1:c.3702A>C
ENST00000683621.1:n.1823A>C
ENST00000683640.1:n.1773A>C
ENST00000684069.1:c.1474A>C	ENSP00000507650.1:p.Arg492=
ENST00000684261.1:c.7954A>C	ENSP00000508097.1:p.Arg2652=
ENST00000684649.1:c.3702A>C
ENST00000262189.11:c.13057A>C MANE Select	ENSP00000262189.6:p.Arg4353=
ENST00000360104.8:c.8844A>C
ENST00000418061.2:c.3699A>C
ENST00000424877.6:c.3633A>C
ENST00000679393.1:n.7768A>C
ENST00000679560.1:c.7957A>C	ENSP00000505094.1:p.Arg2653=
ENST00000679882.1:c.12622A>C	ENSP00000506154.1:p.Arg4208=
ENST00000680029.1:c.3634A>C
ENST00000680877.1:c.7957A>C	ENSP00000505724.1:p.Arg2653=
ENST00000681923.1:n.2072A>C
ENST00000262189.10:c.13057A>C	ENSP00000262189.6:p.Arg4353=
ENST00000355193.6:c.13057A>C	ENSP00000347325.3:p.Arg4353=
ENST00000360104.7:c.5738A>C
ENST00000424877.5:c.2908A>C	ENSP00000410411.1:p.Arg970=
ENST00000473186.5:n.10939A>C
ENST00000558084.5:c.*10577A>C	ENSP00000453752.1:n.*10577A>C
NM_170606.2:c.13057A>C	NP_733751.2:p.Arg4353=
XM_005250025.3:c.13273A>C	XP_005250082.1:p.Arg4425=
XM_005250026.2:c.13270A>C	XP_005250083.1:p.Arg4424=
XM_005250027.3:c.13270A>C	XP_005250084.1:p.Arg4424=
XM_005250028.3:c.13273A>C	XP_005250085.1:p.Arg4425=
XM_005250031.3:c.13108A>C	XP_005250088.1:p.Arg4370=
XM_006716077.2:c.13270A>C	XP_006716140.1:p.Arg4424=
XM_006716078.2:c.13201A>C	XP_006716141.1:p.Arg4401=
XM_006716079.2:c.13105A>C	XP_006716142.1:p.Arg4369=
XM_011516450.1:c.13225A>C	XP_011514752.1:p.Arg4409=
XM_011516451.1:c.13153A>C	XP_011514753.1:p.Arg4385=
XM_011516452.1:c.13120A>C	XP_011514754.1:p.Arg4374=
XM_011516453.1:c.13036A>C	XP_011514755.1:p.Arg4346=
XM_011516454.1:c.12358A>C	XP_011514756.1:p.Arg4120=
XM_011516455.1:c.10819A>C	XP_011514757.1:p.Arg3607=
XM_011516456.1:c.13225A>C	XP_011514758.1:p.Arg4409=
XM_005250025.4:c.13273A>C	XP_005250082.1:p.Arg4425=
XM_005250026.3:c.13270A>C	XP_005250083.1:p.Arg4424=
XM_005250027.4:c.13270A>C	XP_005250084.1:p.Arg4424=
XM_005250028.4:c.13273A>C	XP_005250085.1:p.Arg4425=
XM_005250031.4:c.13108A>C	XP_005250088.1:p.Arg4370=
XM_006716077.3:c.13270A>C	XP_006716140.1:p.Arg4424=
XM_006716078.3:c.13201A>C	XP_006716141.1:p.Arg4401=
XM_006716079.3:c.13105A>C	XP_006716142.1:p.Arg4369=
XM_011516450.2:c.13225A>C	XP_011514752.1:p.Arg4409=
XM_011516451.2:c.13153A>C	XP_011514753.1:p.Arg4385=
XM_011516452.2:c.13120A>C	XP_011514754.1:p.Arg4374=
XM_011516453.2:c.13036A>C	XP_011514755.1:p.Arg4346=
XM_011516454.2:c.12358A>C	XP_011514756.1:p.Arg4120=
XM_011516456.2:c.13225A>C	XP_011514758.1:p.Arg4409=
XM_017012480.1:c.13273A>C	XP_016867969.1:p.Arg4425=
XM_017012481.1:c.13270A>C	XP_016867970.1:p.Arg4424=
XM_017012482.1:c.13270A>C	XP_016867971.1:p.Arg4424=
XM_017012483.1:c.13270A>C	XP_016867972.1:p.Arg4424=
XM_017012484.1:c.13240A>C	XP_016867973.1:p.Arg4414=
XM_017012485.1:c.13222A>C	XP_016867974.1:p.Arg4408=
XM_017012486.1:c.13198A>C	XP_016867975.1:p.Arg4400=
XM_017012487.1:c.13126A>C	XP_016867976.1:p.Arg4376=
XM_017012488.1:c.13090A>C	XP_016867977.1:p.Arg4364=
XM_017012489.1:c.9943A>C	XP_016867978.1:p.Arg3315=
XM_017012490.2:c.9547A>C	XP_016867979.1:p.Arg3183=
XM_024446852.1:c.13270A>C	XP_024302620.1:p.Arg4424=
XM_024446853.1:c.13198A>C	XP_024302621.1:p.Arg4400=
NM_170606.3:c.13057A>C MANE Select	NP_733751.2:p.Arg4353=