Canonical Allele Identifier: CA370093079

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845881A>C (hg19) ; chr7:g.152148796A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148796A>C , CM000669.2:g.152148796A>C	GRCh38
NC_000007.13:g.151845881A>C , CM000669.1:g.151845881A>C	GRCh37
NC_000007.12:g.151476814A>C	NCBI36
NG_033948.1:g.292210T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1319T>G
ENST00000682116.1:n.2263T>G
ENST00000682283.1:c.13302T>G	ENSP00000507485.1:p.Asp4434Glu
ENST00000682629.1:n.2431T>G
ENST00000683120.1:n.8323T>G
ENST00000683178.1:c.3704T>G
ENST00000683200.1:c.10641T>G	ENSP00000508052.1:p.Asp3547Glu
ENST00000683337.1:n.4761T>G
ENST00000683502.1:c.3776T>G
ENST00000683621.1:n.1897T>G
ENST00000683640.1:n.1847T>G
ENST00000684069.1:c.1548T>G	ENSP00000507650.1:p.Asp516Glu
ENST00000684261.1:c.8028T>G	ENSP00000508097.1:p.Asp2676Glu
ENST00000684649.1:c.3776T>G
ENST00000262189.11:c.13131T>G MANE Select	ENSP00000262189.6:p.Asp4377Glu
ENST00000360104.8:c.8918T>G
ENST00000418061.2:c.3773T>G
ENST00000424877.6:c.3707T>G
ENST00000679393.1:n.7842T>G
ENST00000679560.1:c.8031T>G	ENSP00000505094.1:p.Asp2677Glu
ENST00000679882.1:c.12696T>G	ENSP00000506154.1:p.Asp4232Glu
ENST00000680029.1:c.3708T>G
ENST00000680877.1:c.8031T>G	ENSP00000505724.1:p.Asp2677Glu
ENST00000681923.1:n.2146T>G
ENST00000262189.10:c.13131T>G	ENSP00000262189.6:p.Asp4377Glu
ENST00000355193.6:c.13131T>G	ENSP00000347325.3:p.Asp4377Glu
ENST00000360104.7:c.5812T>G
ENST00000424877.5:c.2982T>G	ENSP00000410411.1:p.Asp994Glu
ENST00000473186.5:n.11013T>G
ENST00000558084.5:c.*10651T>G	ENSP00000453752.1:n.*10651T>G
NM_170606.2:c.13131T>G	NP_733751.2:p.Asp4377Glu
XM_005250025.3:c.13347T>G	XP_005250082.1:p.Asp4449Glu
XM_005250026.2:c.13344T>G	XP_005250083.1:p.Asp4448Glu
XM_005250027.3:c.13344T>G	XP_005250084.1:p.Asp4448Glu
XM_005250028.3:c.13347T>G	XP_005250085.1:p.Asp4449Glu
XM_005250031.3:c.13182T>G	XP_005250088.1:p.Asp4394Glu
XM_006716077.2:c.13344T>G	XP_006716140.1:p.Asp4448Glu
XM_006716078.2:c.13275T>G	XP_006716141.1:p.Asp4425Glu
XM_006716079.2:c.13179T>G	XP_006716142.1:p.Asp4393Glu
XM_011516450.1:c.13299T>G	XP_011514752.1:p.Asp4433Glu
XM_011516451.1:c.13227T>G	XP_011514753.1:p.Asp4409Glu
XM_011516452.1:c.13194T>G	XP_011514754.1:p.Asp4398Glu
XM_011516453.1:c.13110T>G	XP_011514755.1:p.Asp4370Glu
XM_011516454.1:c.12432T>G	XP_011514756.1:p.Asp4144Glu
XM_011516455.1:c.10893T>G	XP_011514757.1:p.Asp3631Glu
XM_011516456.1:c.13299T>G	XP_011514758.1:p.Asp4433Glu
XM_005250025.4:c.13347T>G	XP_005250082.1:p.Asp4449Glu
XM_005250026.3:c.13344T>G	XP_005250083.1:p.Asp4448Glu
XM_005250027.4:c.13344T>G	XP_005250084.1:p.Asp4448Glu
XM_005250028.4:c.13347T>G	XP_005250085.1:p.Asp4449Glu
XM_005250031.4:c.13182T>G	XP_005250088.1:p.Asp4394Glu
XM_006716077.3:c.13344T>G	XP_006716140.1:p.Asp4448Glu
XM_006716078.3:c.13275T>G	XP_006716141.1:p.Asp4425Glu
XM_006716079.3:c.13179T>G	XP_006716142.1:p.Asp4393Glu
XM_011516450.2:c.13299T>G	XP_011514752.1:p.Asp4433Glu
XM_011516451.2:c.13227T>G	XP_011514753.1:p.Asp4409Glu
XM_011516452.2:c.13194T>G	XP_011514754.1:p.Asp4398Glu
XM_011516453.2:c.13110T>G	XP_011514755.1:p.Asp4370Glu
XM_011516454.2:c.12432T>G	XP_011514756.1:p.Asp4144Glu
XM_011516456.2:c.13299T>G	XP_011514758.1:p.Asp4433Glu
XM_017012480.1:c.13347T>G	XP_016867969.1:p.Asp4449Glu
XM_017012481.1:c.13344T>G	XP_016867970.1:p.Asp4448Glu
XM_017012482.1:c.13344T>G	XP_016867971.1:p.Asp4448Glu
XM_017012483.1:c.13344T>G	XP_016867972.1:p.Asp4448Glu
XM_017012484.1:c.13314T>G	XP_016867973.1:p.Asp4438Glu
XM_017012485.1:c.13296T>G	XP_016867974.1:p.Asp4432Glu
XM_017012486.1:c.13272T>G	XP_016867975.1:p.Asp4424Glu
XM_017012487.1:c.13200T>G	XP_016867976.1:p.Asp4400Glu
XM_017012488.1:c.13164T>G	XP_016867977.1:p.Asp4388Glu
XM_017012489.1:c.10017T>G	XP_016867978.1:p.Asp3339Glu
XM_017012490.2:c.9621T>G	XP_016867979.1:p.Asp3207Glu
XM_024446852.1:c.13344T>G	XP_024302620.1:p.Asp4448Glu
XM_024446853.1:c.13272T>G	XP_024302621.1:p.Asp4424Glu
NM_170606.3:c.13131T>G MANE Select	NP_733751.2:p.Asp4377Glu