Canonical Allele Identifier: CA370093181

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845912G>A (hg19) ; chr7:g.152148827G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148827G>A , CM000669.2:g.152148827G>A	GRCh38
NC_000007.13:g.151845912G>A , CM000669.1:g.151845912G>A	GRCh37
NC_000007.12:g.151476845G>A	NCBI36
NG_033948.1:g.292179C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1288C>T
ENST00000682116.1:n.2232C>T
ENST00000682283.1:c.13271C>T	ENSP00000507485.1:p.Pro4424Leu
ENST00000682629.1:n.2400C>T
ENST00000683120.1:n.8292C>T
ENST00000683178.1:c.3673C>T
ENST00000683200.1:c.10610C>T	ENSP00000508052.1:p.Pro3537Leu
ENST00000683337.1:n.4730C>T
ENST00000683502.1:c.3745C>T
ENST00000683621.1:n.1866C>T
ENST00000683640.1:n.1816C>T
ENST00000684069.1:c.1517C>T	ENSP00000507650.1:p.Pro506Leu
ENST00000684261.1:c.7997C>T	ENSP00000508097.1:p.Pro2666Leu
ENST00000684649.1:c.3745C>T
ENST00000262189.11:c.13100C>T MANE Select	ENSP00000262189.6:p.Pro4367Leu
ENST00000360104.8:c.8887C>T
ENST00000418061.2:c.3742C>T
ENST00000424877.6:c.3676C>T
ENST00000679393.1:n.7811C>T
ENST00000679560.1:c.8000C>T	ENSP00000505094.1:p.Pro2667Leu
ENST00000679882.1:c.12665C>T	ENSP00000506154.1:p.Pro4222Leu
ENST00000680029.1:c.3677C>T
ENST00000680877.1:c.8000C>T	ENSP00000505724.1:p.Pro2667Leu
ENST00000681923.1:n.2115C>T
ENST00000262189.10:c.13100C>T	ENSP00000262189.6:p.Pro4367Leu
ENST00000355193.6:c.13100C>T	ENSP00000347325.3:p.Pro4367Leu
ENST00000360104.7:c.5781C>T
ENST00000424877.5:c.2951C>T	ENSP00000410411.1:p.Pro984Leu
ENST00000473186.5:n.10982C>T
ENST00000558084.5:c.*10620C>T	ENSP00000453752.1:n.*10620C>T
NM_170606.2:c.13100C>T	NP_733751.2:p.Pro4367Leu
XM_005250025.3:c.13316C>T	XP_005250082.1:p.Pro4439Leu
XM_005250026.2:c.13313C>T	XP_005250083.1:p.Pro4438Leu
XM_005250027.3:c.13313C>T	XP_005250084.1:p.Pro4438Leu
XM_005250028.3:c.13316C>T	XP_005250085.1:p.Pro4439Leu
XM_005250031.3:c.13151C>T	XP_005250088.1:p.Pro4384Leu
XM_006716077.2:c.13313C>T	XP_006716140.1:p.Pro4438Leu
XM_006716078.2:c.13244C>T	XP_006716141.1:p.Pro4415Leu
XM_006716079.2:c.13148C>T	XP_006716142.1:p.Pro4383Leu
XM_011516450.1:c.13268C>T	XP_011514752.1:p.Pro4423Leu
XM_011516451.1:c.13196C>T	XP_011514753.1:p.Pro4399Leu
XM_011516452.1:c.13163C>T	XP_011514754.1:p.Pro4388Leu
XM_011516453.1:c.13079C>T	XP_011514755.1:p.Pro4360Leu
XM_011516454.1:c.12401C>T	XP_011514756.1:p.Pro4134Leu
XM_011516455.1:c.10862C>T	XP_011514757.1:p.Pro3621Leu
XM_011516456.1:c.13268C>T	XP_011514758.1:p.Pro4423Leu
XM_005250025.4:c.13316C>T	XP_005250082.1:p.Pro4439Leu
XM_005250026.3:c.13313C>T	XP_005250083.1:p.Pro4438Leu
XM_005250027.4:c.13313C>T	XP_005250084.1:p.Pro4438Leu
XM_005250028.4:c.13316C>T	XP_005250085.1:p.Pro4439Leu
XM_005250031.4:c.13151C>T	XP_005250088.1:p.Pro4384Leu
XM_006716077.3:c.13313C>T	XP_006716140.1:p.Pro4438Leu
XM_006716078.3:c.13244C>T	XP_006716141.1:p.Pro4415Leu
XM_006716079.3:c.13148C>T	XP_006716142.1:p.Pro4383Leu
XM_011516450.2:c.13268C>T	XP_011514752.1:p.Pro4423Leu
XM_011516451.2:c.13196C>T	XP_011514753.1:p.Pro4399Leu
XM_011516452.2:c.13163C>T	XP_011514754.1:p.Pro4388Leu
XM_011516453.2:c.13079C>T	XP_011514755.1:p.Pro4360Leu
XM_011516454.2:c.12401C>T	XP_011514756.1:p.Pro4134Leu
XM_011516456.2:c.13268C>T	XP_011514758.1:p.Pro4423Leu
XM_017012480.1:c.13316C>T	XP_016867969.1:p.Pro4439Leu
XM_017012481.1:c.13313C>T	XP_016867970.1:p.Pro4438Leu
XM_017012482.1:c.13313C>T	XP_016867971.1:p.Pro4438Leu
XM_017012483.1:c.13313C>T	XP_016867972.1:p.Pro4438Leu
XM_017012484.1:c.13283C>T	XP_016867973.1:p.Pro4428Leu
XM_017012485.1:c.13265C>T	XP_016867974.1:p.Pro4422Leu
XM_017012486.1:c.13241C>T	XP_016867975.1:p.Pro4414Leu
XM_017012487.1:c.13169C>T	XP_016867976.1:p.Pro4390Leu
XM_017012488.1:c.13133C>T	XP_016867977.1:p.Pro4378Leu
XM_017012489.1:c.9986C>T	XP_016867978.1:p.Pro3329Leu
XM_017012490.2:c.9590C>T	XP_016867979.1:p.Pro3197Leu
XM_024446852.1:c.13313C>T	XP_024302620.1:p.Pro4438Leu
XM_024446853.1:c.13241C>T	XP_024302621.1:p.Pro4414Leu
NM_170606.3:c.13100C>T MANE Select	NP_733751.2:p.Pro4367Leu