Canonical Allele Identifier: CA370093317

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845949T>A (hg19) ; chr7:g.152148864T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148864T>A , CM000669.2:g.152148864T>A	GRCh38
NC_000007.13:g.151845949T>A , CM000669.1:g.151845949T>A	GRCh37
NC_000007.12:g.151476882T>A	NCBI36
NG_033948.1:g.292142A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1251A>T
ENST00000682116.1:n.2195A>T
ENST00000682283.1:c.13234A>T	ENSP00000507485.1:p.Met4412Leu
ENST00000682629.1:n.2363A>T
ENST00000683120.1:n.8255A>T
ENST00000683178.1:c.3636A>T
ENST00000683200.1:c.10573A>T	ENSP00000508052.1:p.Met3525Leu
ENST00000683337.1:n.4693A>T
ENST00000683502.1:c.3708A>T
ENST00000683621.1:n.1829A>T
ENST00000683640.1:n.1779A>T
ENST00000684069.1:c.1480A>T	ENSP00000507650.1:p.Met494Leu
ENST00000684261.1:c.7960A>T	ENSP00000508097.1:p.Met2654Leu
ENST00000684649.1:c.3708A>T
ENST00000262189.11:c.13063A>T MANE Select	ENSP00000262189.6:p.Met4355Leu
ENST00000360104.8:c.8850A>T
ENST00000418061.2:c.3705A>T
ENST00000424877.6:c.3639A>T
ENST00000679393.1:n.7774A>T
ENST00000679560.1:c.7963A>T	ENSP00000505094.1:p.Met2655Leu
ENST00000679882.1:c.12628A>T	ENSP00000506154.1:p.Met4210Leu
ENST00000680029.1:c.3640A>T
ENST00000680877.1:c.7963A>T	ENSP00000505724.1:p.Met2655Leu
ENST00000681923.1:n.2078A>T
ENST00000262189.10:c.13063A>T	ENSP00000262189.6:p.Met4355Leu
ENST00000355193.6:c.13063A>T	ENSP00000347325.3:p.Met4355Leu
ENST00000360104.7:c.5744A>T
ENST00000424877.5:c.2914A>T	ENSP00000410411.1:p.Met972Leu
ENST00000473186.5:n.10945A>T
ENST00000558084.5:c.*10583A>T	ENSP00000453752.1:n.*10583A>T
NM_170606.2:c.13063A>T	NP_733751.2:p.Met4355Leu
XM_005250025.3:c.13279A>T	XP_005250082.1:p.Met4427Leu
XM_005250026.2:c.13276A>T	XP_005250083.1:p.Met4426Leu
XM_005250027.3:c.13276A>T	XP_005250084.1:p.Met4426Leu
XM_005250028.3:c.13279A>T	XP_005250085.1:p.Met4427Leu
XM_005250031.3:c.13114A>T	XP_005250088.1:p.Met4372Leu
XM_006716077.2:c.13276A>T	XP_006716140.1:p.Met4426Leu
XM_006716078.2:c.13207A>T	XP_006716141.1:p.Met4403Leu
XM_006716079.2:c.13111A>T	XP_006716142.1:p.Met4371Leu
XM_011516450.1:c.13231A>T	XP_011514752.1:p.Met4411Leu
XM_011516451.1:c.13159A>T	XP_011514753.1:p.Met4387Leu
XM_011516452.1:c.13126A>T	XP_011514754.1:p.Met4376Leu
XM_011516453.1:c.13042A>T	XP_011514755.1:p.Met4348Leu
XM_011516454.1:c.12364A>T	XP_011514756.1:p.Met4122Leu
XM_011516455.1:c.10825A>T	XP_011514757.1:p.Met3609Leu
XM_011516456.1:c.13231A>T	XP_011514758.1:p.Met4411Leu
XM_005250025.4:c.13279A>T	XP_005250082.1:p.Met4427Leu
XM_005250026.3:c.13276A>T	XP_005250083.1:p.Met4426Leu
XM_005250027.4:c.13276A>T	XP_005250084.1:p.Met4426Leu
XM_005250028.4:c.13279A>T	XP_005250085.1:p.Met4427Leu
XM_005250031.4:c.13114A>T	XP_005250088.1:p.Met4372Leu
XM_006716077.3:c.13276A>T	XP_006716140.1:p.Met4426Leu
XM_006716078.3:c.13207A>T	XP_006716141.1:p.Met4403Leu
XM_006716079.3:c.13111A>T	XP_006716142.1:p.Met4371Leu
XM_011516450.2:c.13231A>T	XP_011514752.1:p.Met4411Leu
XM_011516451.2:c.13159A>T	XP_011514753.1:p.Met4387Leu
XM_011516452.2:c.13126A>T	XP_011514754.1:p.Met4376Leu
XM_011516453.2:c.13042A>T	XP_011514755.1:p.Met4348Leu
XM_011516454.2:c.12364A>T	XP_011514756.1:p.Met4122Leu
XM_011516456.2:c.13231A>T	XP_011514758.1:p.Met4411Leu
XM_017012480.1:c.13279A>T	XP_016867969.1:p.Met4427Leu
XM_017012481.1:c.13276A>T	XP_016867970.1:p.Met4426Leu
XM_017012482.1:c.13276A>T	XP_016867971.1:p.Met4426Leu
XM_017012483.1:c.13276A>T	XP_016867972.1:p.Met4426Leu
XM_017012484.1:c.13246A>T	XP_016867973.1:p.Met4416Leu
XM_017012485.1:c.13228A>T	XP_016867974.1:p.Met4410Leu
XM_017012486.1:c.13204A>T	XP_016867975.1:p.Met4402Leu
XM_017012487.1:c.13132A>T	XP_016867976.1:p.Met4378Leu
XM_017012488.1:c.13096A>T	XP_016867977.1:p.Met4366Leu
XM_017012489.1:c.9949A>T	XP_016867978.1:p.Met3317Leu
XM_017012490.2:c.9553A>T	XP_016867979.1:p.Met3185Leu
XM_024446852.1:c.13276A>T	XP_024302620.1:p.Met4426Leu
XM_024446853.1:c.13204A>T	XP_024302621.1:p.Met4402Leu
NM_170606.3:c.13063A>T MANE Select	NP_733751.2:p.Met4355Leu