Canonical Allele Identifier: CA370093355

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845959T>G (hg19) ; chr7:g.152148874T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148874T>G , CM000669.2:g.152148874T>G	GRCh38
NC_000007.13:g.151845959T>G , CM000669.1:g.151845959T>G	GRCh37
NC_000007.12:g.151476892T>G	NCBI36
NG_033948.1:g.292132A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1241A>C
ENST00000682116.1:n.2185A>C
ENST00000682283.1:c.13224A>C	ENSP00000507485.1:p.Lys4408Asn
ENST00000682629.1:n.2353A>C
ENST00000683120.1:n.8245A>C
ENST00000683178.1:c.3626A>C
ENST00000683200.1:c.10563A>C	ENSP00000508052.1:p.Lys3521Asn
ENST00000683337.1:n.4683A>C
ENST00000683502.1:c.3698A>C
ENST00000683621.1:n.1819A>C
ENST00000683640.1:n.1769A>C
ENST00000684069.1:c.1470A>C	ENSP00000507650.1:p.Lys490Asn
ENST00000684261.1:c.7950A>C	ENSP00000508097.1:p.Lys2650Asn
ENST00000684649.1:c.3698A>C
ENST00000262189.11:c.13053A>C MANE Select	ENSP00000262189.6:p.Lys4351Asn
ENST00000360104.8:c.8840A>C
ENST00000418061.2:c.3695A>C
ENST00000424877.6:c.3629A>C
ENST00000679393.1:n.7764A>C
ENST00000679560.1:c.7953A>C	ENSP00000505094.1:p.Lys2651Asn
ENST00000679882.1:c.12618A>C	ENSP00000506154.1:p.Lys4206Asn
ENST00000680029.1:c.3630A>C
ENST00000680877.1:c.7953A>C	ENSP00000505724.1:p.Lys2651Asn
ENST00000681923.1:n.2068A>C
ENST00000262189.10:c.13053A>C	ENSP00000262189.6:p.Lys4351Asn
ENST00000355193.6:c.13053A>C	ENSP00000347325.3:p.Lys4351Asn
ENST00000360104.7:c.5734A>C
ENST00000424877.5:c.2904A>C	ENSP00000410411.1:p.Lys968Asn
ENST00000473186.5:n.10935A>C
ENST00000558084.5:c.*10573A>C	ENSP00000453752.1:n.*10573A>C
NM_170606.2:c.13053A>C	NP_733751.2:p.Lys4351Asn
XM_005250025.3:c.13269A>C	XP_005250082.1:p.Lys4423Asn
XM_005250026.2:c.13266A>C	XP_005250083.1:p.Lys4422Asn
XM_005250027.3:c.13266A>C	XP_005250084.1:p.Lys4422Asn
XM_005250028.3:c.13269A>C	XP_005250085.1:p.Lys4423Asn
XM_005250031.3:c.13104A>C	XP_005250088.1:p.Lys4368Asn
XM_006716077.2:c.13266A>C	XP_006716140.1:p.Lys4422Asn
XM_006716078.2:c.13197A>C	XP_006716141.1:p.Lys4399Asn
XM_006716079.2:c.13101A>C	XP_006716142.1:p.Lys4367Asn
XM_011516450.1:c.13221A>C	XP_011514752.1:p.Lys4407Asn
XM_011516451.1:c.13149A>C	XP_011514753.1:p.Lys4383Asn
XM_011516452.1:c.13116A>C	XP_011514754.1:p.Lys4372Asn
XM_011516453.1:c.13032A>C	XP_011514755.1:p.Lys4344Asn
XM_011516454.1:c.12354A>C	XP_011514756.1:p.Lys4118Asn
XM_011516455.1:c.10815A>C	XP_011514757.1:p.Lys3605Asn
XM_011516456.1:c.13221A>C	XP_011514758.1:p.Lys4407Asn
XM_005250025.4:c.13269A>C	XP_005250082.1:p.Lys4423Asn
XM_005250026.3:c.13266A>C	XP_005250083.1:p.Lys4422Asn
XM_005250027.4:c.13266A>C	XP_005250084.1:p.Lys4422Asn
XM_005250028.4:c.13269A>C	XP_005250085.1:p.Lys4423Asn
XM_005250031.4:c.13104A>C	XP_005250088.1:p.Lys4368Asn
XM_006716077.3:c.13266A>C	XP_006716140.1:p.Lys4422Asn
XM_006716078.3:c.13197A>C	XP_006716141.1:p.Lys4399Asn
XM_006716079.3:c.13101A>C	XP_006716142.1:p.Lys4367Asn
XM_011516450.2:c.13221A>C	XP_011514752.1:p.Lys4407Asn
XM_011516451.2:c.13149A>C	XP_011514753.1:p.Lys4383Asn
XM_011516452.2:c.13116A>C	XP_011514754.1:p.Lys4372Asn
XM_011516453.2:c.13032A>C	XP_011514755.1:p.Lys4344Asn
XM_011516454.2:c.12354A>C	XP_011514756.1:p.Lys4118Asn
XM_011516456.2:c.13221A>C	XP_011514758.1:p.Lys4407Asn
XM_017012480.1:c.13269A>C	XP_016867969.1:p.Lys4423Asn
XM_017012481.1:c.13266A>C	XP_016867970.1:p.Lys4422Asn
XM_017012482.1:c.13266A>C	XP_016867971.1:p.Lys4422Asn
XM_017012483.1:c.13266A>C	XP_016867972.1:p.Lys4422Asn
XM_017012484.1:c.13236A>C	XP_016867973.1:p.Lys4412Asn
XM_017012485.1:c.13218A>C	XP_016867974.1:p.Lys4406Asn
XM_017012486.1:c.13194A>C	XP_016867975.1:p.Lys4398Asn
XM_017012487.1:c.13122A>C	XP_016867976.1:p.Lys4374Asn
XM_017012488.1:c.13086A>C	XP_016867977.1:p.Lys4362Asn
XM_017012489.1:c.9939A>C	XP_016867978.1:p.Lys3313Asn
XM_017012490.2:c.9543A>C	XP_016867979.1:p.Lys3181Asn
XM_024446852.1:c.13266A>C	XP_024302620.1:p.Lys4422Asn
XM_024446853.1:c.13194A>C	XP_024302621.1:p.Lys4398Asn
NM_170606.3:c.13053A>C MANE Select	NP_733751.2:p.Lys4351Asn