Canonical Allele Identifier: CA370091826

Gene: KMT2C

Linked Data

• COSMIC: COSM3785043 ; COSM3785044
• MyVariant Identifiers: chr7:g.151845760T>C (hg19) ; chr7:g.152148675T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148675T>C , CM000669.2:g.152148675T>C	GRCh38
NC_000007.13:g.151845760T>C , CM000669.1:g.151845760T>C	GRCh37
NC_000007.12:g.151476693T>C	NCBI36
NG_033948.1:g.292331A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682040.1:c.1440A>G
ENST00000682116.1:n.2384A>G
ENST00000682283.1:c.13423A>G	ENSP00000507485.1:p.Arg4475Gly
ENST00000682629.1:n.2552A>G
ENST00000683120.1:n.8444A>G
ENST00000683178.1:c.3825A>G
ENST00000683200.1:c.10762A>G	ENSP00000508052.1:p.Arg3588Gly
ENST00000683337.1:n.4882A>G
ENST00000683502.1:c.3897A>G
ENST00000683621.1:n.2018A>G
ENST00000683640.1:n.1968A>G
ENST00000684069.1:c.1669A>G	ENSP00000507650.1:p.Arg557Gly
ENST00000684261.1:c.8149A>G	ENSP00000508097.1:p.Arg2717Gly
ENST00000684391.1:n.10A>G
ENST00000684649.1:c.3897A>G
ENST00000262189.11:c.13252A>G MANE Select	ENSP00000262189.6:p.Arg4418Gly
ENST00000360104.8:c.9039A>G
ENST00000418061.2:c.3894A>G
ENST00000424877.6:c.3828A>G
ENST00000679393.1:n.7963A>G
ENST00000679560.1:c.8152A>G	ENSP00000505094.1:p.Arg2718Gly
ENST00000679882.1:c.12817A>G	ENSP00000506154.1:p.Arg4273Gly
ENST00000680029.1:c.3829A>G
ENST00000680877.1:c.8152A>G	ENSP00000505724.1:p.Arg2718Gly
ENST00000681923.1:n.2267A>G
ENST00000262189.10:c.13252A>G	ENSP00000262189.6:p.Arg4418Gly
ENST00000355193.6:c.13252A>G	ENSP00000347325.3:p.Arg4418Gly
ENST00000360104.7:c.5933A>G
ENST00000424877.5:c.3103A>G	ENSP00000410411.1:p.Arg1035Gly
ENST00000473186.5:n.11134A>G
ENST00000558084.5:c.*10772A>G	ENSP00000453752.1:n.*10772A>G
NM_170606.2:c.13252A>G	NP_733751.2:p.Arg4418Gly
XM_005250025.3:c.13468A>G	XP_005250082.1:p.Arg4490Gly
XM_005250026.2:c.13465A>G	XP_005250083.1:p.Arg4489Gly
XM_005250027.3:c.13465A>G	XP_005250084.1:p.Arg4489Gly
XM_005250028.3:c.13468A>G	XP_005250085.1:p.Arg4490Gly
XM_005250031.3:c.13303A>G	XP_005250088.1:p.Arg4435Gly
XM_006716077.2:c.13465A>G	XP_006716140.1:p.Arg4489Gly
XM_006716078.2:c.13396A>G	XP_006716141.1:p.Arg4466Gly
XM_006716079.2:c.13300A>G	XP_006716142.1:p.Arg4434Gly
XM_011516450.1:c.13420A>G	XP_011514752.1:p.Arg4474Gly
XM_011516451.1:c.13348A>G	XP_011514753.1:p.Arg4450Gly
XM_011516452.1:c.13315A>G	XP_011514754.1:p.Arg4439Gly
XM_011516453.1:c.13231A>G	XP_011514755.1:p.Arg4411Gly
XM_011516454.1:c.12553A>G	XP_011514756.1:p.Arg4185Gly
XM_011516455.1:c.11014A>G	XP_011514757.1:p.Arg3672Gly
XM_011516456.1:c.13420A>G	XP_011514758.1:p.Arg4474Gly
XM_005250025.4:c.13468A>G	XP_005250082.1:p.Arg4490Gly
XM_005250026.3:c.13465A>G	XP_005250083.1:p.Arg4489Gly
XM_005250027.4:c.13465A>G	XP_005250084.1:p.Arg4489Gly
XM_005250028.4:c.13468A>G	XP_005250085.1:p.Arg4490Gly
XM_005250031.4:c.13303A>G	XP_005250088.1:p.Arg4435Gly
XM_006716077.3:c.13465A>G	XP_006716140.1:p.Arg4489Gly
XM_006716078.3:c.13396A>G	XP_006716141.1:p.Arg4466Gly
XM_006716079.3:c.13300A>G	XP_006716142.1:p.Arg4434Gly
XM_011516450.2:c.13420A>G	XP_011514752.1:p.Arg4474Gly
XM_011516451.2:c.13348A>G	XP_011514753.1:p.Arg4450Gly
XM_011516452.2:c.13315A>G	XP_011514754.1:p.Arg4439Gly
XM_011516453.2:c.13231A>G	XP_011514755.1:p.Arg4411Gly
XM_011516454.2:c.12553A>G	XP_011514756.1:p.Arg4185Gly
XM_011516456.2:c.13420A>G	XP_011514758.1:p.Arg4474Gly
XM_017012480.1:c.13468A>G	XP_016867969.1:p.Arg4490Gly
XM_017012481.1:c.13465A>G	XP_016867970.1:p.Arg4489Gly
XM_017012482.1:c.13465A>G	XP_016867971.1:p.Arg4489Gly
XM_017012483.1:c.13465A>G	XP_016867972.1:p.Arg4489Gly
XM_017012484.1:c.13435A>G	XP_016867973.1:p.Arg4479Gly
XM_017012485.1:c.13417A>G	XP_016867974.1:p.Arg4473Gly
XM_017012486.1:c.13393A>G	XP_016867975.1:p.Arg4465Gly
XM_017012487.1:c.13321A>G	XP_016867976.1:p.Arg4441Gly
XM_017012488.1:c.13285A>G	XP_016867977.1:p.Arg4429Gly
XM_017012489.1:c.10138A>G	XP_016867978.1:p.Arg3380Gly
XM_017012490.2:c.9742A>G	XP_016867979.1:p.Arg3248Gly
XM_024446852.1:c.13465A>G	XP_024302620.1:p.Arg4489Gly
XM_024446853.1:c.13393A>G	XP_024302621.1:p.Arg4465Gly
NM_170606.3:c.13252A>G MANE Select	NP_733751.2:p.Arg4418Gly