Canonical Allele Identifier: CA370091824

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845760T>A (hg19) ; chr7:g.152148675T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000682040.1:c.1440A>T
ENST00000682116.1:n.2384A>T
ENST00000682283.1:c.13423A>T	ENSP00000507485.1:p.Arg4475Trp
ENST00000682629.1:n.2552A>T
ENST00000683120.1:n.8444A>T
ENST00000683178.1:c.3825A>T
ENST00000683200.1:c.10762A>T	ENSP00000508052.1:p.Arg3588Trp
ENST00000683337.1:n.4882A>T
ENST00000683502.1:c.3897A>T
ENST00000683621.1:n.2018A>T
ENST00000683640.1:n.1968A>T
ENST00000684069.1:c.1669A>T	ENSP00000507650.1:p.Arg557Trp
ENST00000684261.1:c.8149A>T	ENSP00000508097.1:p.Arg2717Trp
ENST00000684391.1:n.10A>T
ENST00000684649.1:c.3897A>T
ENST00000262189.11:c.13252A>T MANE Select	ENSP00000262189.6:p.Arg4418Trp
ENST00000360104.8:c.9039A>T
ENST00000418061.2:c.3894A>T
ENST00000424877.6:c.3828A>T
ENST00000679393.1:n.7963A>T
ENST00000679560.1:c.8152A>T	ENSP00000505094.1:p.Arg2718Trp
ENST00000679882.1:c.12817A>T	ENSP00000506154.1:p.Arg4273Trp
ENST00000680029.1:c.3829A>T
ENST00000680877.1:c.8152A>T	ENSP00000505724.1:p.Arg2718Trp
ENST00000681923.1:n.2267A>T
ENST00000262189.10:c.13252A>T	ENSP00000262189.6:p.Arg4418Trp
ENST00000355193.6:c.13252A>T	ENSP00000347325.3:p.Arg4418Trp
ENST00000360104.7:c.5933A>T
ENST00000424877.5:c.3103A>T	ENSP00000410411.1:p.Arg1035Trp
ENST00000473186.5:n.11134A>T
ENST00000558084.5:c.*10772A>T	ENSP00000453752.1:n.*10772A>T
NM_170606.2:c.13252A>T	NP_733751.2:p.Arg4418Trp
XM_005250025.3:c.13468A>T	XP_005250082.1:p.Arg4490Trp
XM_005250026.2:c.13465A>T	XP_005250083.1:p.Arg4489Trp
XM_005250027.3:c.13465A>T	XP_005250084.1:p.Arg4489Trp
XM_005250028.3:c.13468A>T	XP_005250085.1:p.Arg4490Trp
XM_005250031.3:c.13303A>T	XP_005250088.1:p.Arg4435Trp
XM_006716077.2:c.13465A>T	XP_006716140.1:p.Arg4489Trp
XM_006716078.2:c.13396A>T	XP_006716141.1:p.Arg4466Trp
XM_006716079.2:c.13300A>T	XP_006716142.1:p.Arg4434Trp
XM_011516450.1:c.13420A>T	XP_011514752.1:p.Arg4474Trp
XM_011516451.1:c.13348A>T	XP_011514753.1:p.Arg4450Trp
XM_011516452.1:c.13315A>T	XP_011514754.1:p.Arg4439Trp
XM_011516453.1:c.13231A>T	XP_011514755.1:p.Arg4411Trp
XM_011516454.1:c.12553A>T	XP_011514756.1:p.Arg4185Trp
XM_011516455.1:c.11014A>T	XP_011514757.1:p.Arg3672Trp
XM_011516456.1:c.13420A>T	XP_011514758.1:p.Arg4474Trp
XM_005250025.4:c.13468A>T	XP_005250082.1:p.Arg4490Trp
XM_005250026.3:c.13465A>T	XP_005250083.1:p.Arg4489Trp
XM_005250027.4:c.13465A>T	XP_005250084.1:p.Arg4489Trp
XM_005250028.4:c.13468A>T	XP_005250085.1:p.Arg4490Trp
XM_005250031.4:c.13303A>T	XP_005250088.1:p.Arg4435Trp
XM_006716077.3:c.13465A>T	XP_006716140.1:p.Arg4489Trp
XM_006716078.3:c.13396A>T	XP_006716141.1:p.Arg4466Trp
XM_006716079.3:c.13300A>T	XP_006716142.1:p.Arg4434Trp
XM_011516450.2:c.13420A>T	XP_011514752.1:p.Arg4474Trp
XM_011516451.2:c.13348A>T	XP_011514753.1:p.Arg4450Trp
XM_011516452.2:c.13315A>T	XP_011514754.1:p.Arg4439Trp
XM_011516453.2:c.13231A>T	XP_011514755.1:p.Arg4411Trp
XM_011516454.2:c.12553A>T	XP_011514756.1:p.Arg4185Trp
XM_011516456.2:c.13420A>T	XP_011514758.1:p.Arg4474Trp
XM_017012480.1:c.13468A>T	XP_016867969.1:p.Arg4490Trp
XM_017012481.1:c.13465A>T	XP_016867970.1:p.Arg4489Trp
XM_017012482.1:c.13465A>T	XP_016867971.1:p.Arg4489Trp
XM_017012483.1:c.13465A>T	XP_016867972.1:p.Arg4489Trp
XM_017012484.1:c.13435A>T	XP_016867973.1:p.Arg4479Trp
XM_017012485.1:c.13417A>T	XP_016867974.1:p.Arg4473Trp
XM_017012486.1:c.13393A>T	XP_016867975.1:p.Arg4465Trp
XM_017012487.1:c.13321A>T	XP_016867976.1:p.Arg4441Trp
XM_017012488.1:c.13285A>T	XP_016867977.1:p.Arg4429Trp
XM_017012489.1:c.10138A>T	XP_016867978.1:p.Arg3380Trp
XM_017012490.2:c.9742A>T	XP_016867979.1:p.Arg3248Trp
XM_024446852.1:c.13465A>T	XP_024302620.1:p.Arg4489Trp
XM_024446853.1:c.13393A>T	XP_024302621.1:p.Arg4465Trp
NM_170606.3:c.13252A>T MANE Select	NP_733751.2:p.Arg4418Trp