Canonical Allele Identifier: CA370093172

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845908C>G (hg19) ; chr7:g.152148823C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148823C>G , CM000669.2:g.152148823C>G	GRCh38
NC_000007.13:g.151845908C>G , CM000669.1:g.151845908C>G	GRCh37
NC_000007.12:g.151476841C>G	NCBI36
NG_033948.1:g.292183G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1292G>C
ENST00000682116.1:n.2236G>C
ENST00000682283.1:c.13275G>C	ENSP00000507485.1:p.Lys4425Asn
ENST00000682629.1:n.2404G>C
ENST00000683120.1:n.8296G>C
ENST00000683178.1:c.3677G>C
ENST00000683200.1:c.10614G>C	ENSP00000508052.1:p.Lys3538Asn
ENST00000683337.1:n.4734G>C
ENST00000683502.1:c.3749G>C
ENST00000683621.1:n.1870G>C
ENST00000683640.1:n.1820G>C
ENST00000684069.1:c.1521G>C	ENSP00000507650.1:p.Lys507Asn
ENST00000684261.1:c.8001G>C	ENSP00000508097.1:p.Lys2667Asn
ENST00000684649.1:c.3749G>C
ENST00000262189.11:c.13104G>C MANE Select	ENSP00000262189.6:p.Lys4368Asn
ENST00000360104.8:c.8891G>C
ENST00000418061.2:c.3746G>C
ENST00000424877.6:c.3680G>C
ENST00000679393.1:n.7815G>C
ENST00000679560.1:c.8004G>C	ENSP00000505094.1:p.Lys2668Asn
ENST00000679882.1:c.12669G>C	ENSP00000506154.1:p.Lys4223Asn
ENST00000680029.1:c.3681G>C
ENST00000680877.1:c.8004G>C	ENSP00000505724.1:p.Lys2668Asn
ENST00000681923.1:n.2119G>C
ENST00000262189.10:c.13104G>C	ENSP00000262189.6:p.Lys4368Asn
ENST00000355193.6:c.13104G>C	ENSP00000347325.3:p.Lys4368Asn
ENST00000360104.7:c.5785G>C
ENST00000424877.5:c.2955G>C	ENSP00000410411.1:p.Lys985Asn
ENST00000473186.5:n.10986G>C
ENST00000558084.5:c.*10624G>C	ENSP00000453752.1:n.*10624G>C
NM_170606.2:c.13104G>C	NP_733751.2:p.Lys4368Asn
XM_005250025.3:c.13320G>C	XP_005250082.1:p.Lys4440Asn
XM_005250026.2:c.13317G>C	XP_005250083.1:p.Lys4439Asn
XM_005250027.3:c.13317G>C	XP_005250084.1:p.Lys4439Asn
XM_005250028.3:c.13320G>C	XP_005250085.1:p.Lys4440Asn
XM_005250031.3:c.13155G>C	XP_005250088.1:p.Lys4385Asn
XM_006716077.2:c.13317G>C	XP_006716140.1:p.Lys4439Asn
XM_006716078.2:c.13248G>C	XP_006716141.1:p.Lys4416Asn
XM_006716079.2:c.13152G>C	XP_006716142.1:p.Lys4384Asn
XM_011516450.1:c.13272G>C	XP_011514752.1:p.Lys4424Asn
XM_011516451.1:c.13200G>C	XP_011514753.1:p.Lys4400Asn
XM_011516452.1:c.13167G>C	XP_011514754.1:p.Lys4389Asn
XM_011516453.1:c.13083G>C	XP_011514755.1:p.Lys4361Asn
XM_011516454.1:c.12405G>C	XP_011514756.1:p.Lys4135Asn
XM_011516455.1:c.10866G>C	XP_011514757.1:p.Lys3622Asn
XM_011516456.1:c.13272G>C	XP_011514758.1:p.Lys4424Asn
XM_005250025.4:c.13320G>C	XP_005250082.1:p.Lys4440Asn
XM_005250026.3:c.13317G>C	XP_005250083.1:p.Lys4439Asn
XM_005250027.4:c.13317G>C	XP_005250084.1:p.Lys4439Asn
XM_005250028.4:c.13320G>C	XP_005250085.1:p.Lys4440Asn
XM_005250031.4:c.13155G>C	XP_005250088.1:p.Lys4385Asn
XM_006716077.3:c.13317G>C	XP_006716140.1:p.Lys4439Asn
XM_006716078.3:c.13248G>C	XP_006716141.1:p.Lys4416Asn
XM_006716079.3:c.13152G>C	XP_006716142.1:p.Lys4384Asn
XM_011516450.2:c.13272G>C	XP_011514752.1:p.Lys4424Asn
XM_011516451.2:c.13200G>C	XP_011514753.1:p.Lys4400Asn
XM_011516452.2:c.13167G>C	XP_011514754.1:p.Lys4389Asn
XM_011516453.2:c.13083G>C	XP_011514755.1:p.Lys4361Asn
XM_011516454.2:c.12405G>C	XP_011514756.1:p.Lys4135Asn
XM_011516456.2:c.13272G>C	XP_011514758.1:p.Lys4424Asn
XM_017012480.1:c.13320G>C	XP_016867969.1:p.Lys4440Asn
XM_017012481.1:c.13317G>C	XP_016867970.1:p.Lys4439Asn
XM_017012482.1:c.13317G>C	XP_016867971.1:p.Lys4439Asn
XM_017012483.1:c.13317G>C	XP_016867972.1:p.Lys4439Asn
XM_017012484.1:c.13287G>C	XP_016867973.1:p.Lys4429Asn
XM_017012485.1:c.13269G>C	XP_016867974.1:p.Lys4423Asn
XM_017012486.1:c.13245G>C	XP_016867975.1:p.Lys4415Asn
XM_017012487.1:c.13173G>C	XP_016867976.1:p.Lys4391Asn
XM_017012488.1:c.13137G>C	XP_016867977.1:p.Lys4379Asn
XM_017012489.1:c.9990G>C	XP_016867978.1:p.Lys3330Asn
XM_017012490.2:c.9594G>C	XP_016867979.1:p.Lys3198Asn
XM_024446852.1:c.13317G>C	XP_024302620.1:p.Lys4439Asn
XM_024446853.1:c.13245G>C	XP_024302621.1:p.Lys4415Asn
NM_170606.3:c.13104G>C MANE Select	NP_733751.2:p.Lys4368Asn