Canonical Allele Identifier: CA370093320

Gene: KMT2C

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1251A>G
ENST00000682116.1:n.2195A>G
ENST00000682283.1:c.13234A>G	ENSP00000507485.1:p.Met4412Val
ENST00000682629.1:n.2363A>G
ENST00000683120.1:n.8255A>G
ENST00000683178.1:c.3636A>G
ENST00000683200.1:c.10573A>G	ENSP00000508052.1:p.Met3525Val
ENST00000683337.1:n.4693A>G
ENST00000683502.1:c.3708A>G
ENST00000683621.1:n.1829A>G
ENST00000683640.1:n.1779A>G
ENST00000684069.1:c.1480A>G	ENSP00000507650.1:p.Met494Val
ENST00000684261.1:c.7960A>G	ENSP00000508097.1:p.Met2654Val
ENST00000684649.1:c.3708A>G
ENST00000262189.11:c.13063A>G MANE Select	ENSP00000262189.6:p.Met4355Val
ENST00000360104.8:c.8850A>G
ENST00000418061.2:c.3705A>G
ENST00000424877.6:c.3639A>G
ENST00000679393.1:n.7774A>G
ENST00000679560.1:c.7963A>G	ENSP00000505094.1:p.Met2655Val
ENST00000679882.1:c.12628A>G	ENSP00000506154.1:p.Met4210Val
ENST00000680029.1:c.3640A>G
ENST00000680877.1:c.7963A>G	ENSP00000505724.1:p.Met2655Val
ENST00000681923.1:n.2078A>G
ENST00000262189.10:c.13063A>G	ENSP00000262189.6:p.Met4355Val
ENST00000355193.6:c.13063A>G	ENSP00000347325.3:p.Met4355Val
ENST00000360104.7:c.5744A>G
ENST00000424877.5:c.2914A>G	ENSP00000410411.1:p.Met972Val
ENST00000473186.5:n.10945A>G
ENST00000558084.5:c.*10583A>G	ENSP00000453752.1:n.*10583A>G
NM_170606.2:c.13063A>G	NP_733751.2:p.Met4355Val
XM_005250025.3:c.13279A>G	XP_005250082.1:p.Met4427Val
XM_005250026.2:c.13276A>G	XP_005250083.1:p.Met4426Val
XM_005250027.3:c.13276A>G	XP_005250084.1:p.Met4426Val
XM_005250028.3:c.13279A>G	XP_005250085.1:p.Met4427Val
XM_005250031.3:c.13114A>G	XP_005250088.1:p.Met4372Val
XM_006716077.2:c.13276A>G	XP_006716140.1:p.Met4426Val
XM_006716078.2:c.13207A>G	XP_006716141.1:p.Met4403Val
XM_006716079.2:c.13111A>G	XP_006716142.1:p.Met4371Val
XM_011516450.1:c.13231A>G	XP_011514752.1:p.Met4411Val
XM_011516451.1:c.13159A>G	XP_011514753.1:p.Met4387Val
XM_011516452.1:c.13126A>G	XP_011514754.1:p.Met4376Val
XM_011516453.1:c.13042A>G	XP_011514755.1:p.Met4348Val
XM_011516454.1:c.12364A>G	XP_011514756.1:p.Met4122Val
XM_011516455.1:c.10825A>G	XP_011514757.1:p.Met3609Val
XM_011516456.1:c.13231A>G	XP_011514758.1:p.Met4411Val
XM_005250025.4:c.13279A>G	XP_005250082.1:p.Met4427Val
XM_005250026.3:c.13276A>G	XP_005250083.1:p.Met4426Val
XM_005250027.4:c.13276A>G	XP_005250084.1:p.Met4426Val
XM_005250028.4:c.13279A>G	XP_005250085.1:p.Met4427Val
XM_005250031.4:c.13114A>G	XP_005250088.1:p.Met4372Val
XM_006716077.3:c.13276A>G	XP_006716140.1:p.Met4426Val
XM_006716078.3:c.13207A>G	XP_006716141.1:p.Met4403Val
XM_006716079.3:c.13111A>G	XP_006716142.1:p.Met4371Val
XM_011516450.2:c.13231A>G	XP_011514752.1:p.Met4411Val
XM_011516451.2:c.13159A>G	XP_011514753.1:p.Met4387Val
XM_011516452.2:c.13126A>G	XP_011514754.1:p.Met4376Val
XM_011516453.2:c.13042A>G	XP_011514755.1:p.Met4348Val
XM_011516454.2:c.12364A>G	XP_011514756.1:p.Met4122Val
XM_011516456.2:c.13231A>G	XP_011514758.1:p.Met4411Val
XM_017012480.1:c.13279A>G	XP_016867969.1:p.Met4427Val
XM_017012481.1:c.13276A>G	XP_016867970.1:p.Met4426Val
XM_017012482.1:c.13276A>G	XP_016867971.1:p.Met4426Val
XM_017012483.1:c.13276A>G	XP_016867972.1:p.Met4426Val
XM_017012484.1:c.13246A>G	XP_016867973.1:p.Met4416Val
XM_017012485.1:c.13228A>G	XP_016867974.1:p.Met4410Val
XM_017012486.1:c.13204A>G	XP_016867975.1:p.Met4402Val
XM_017012487.1:c.13132A>G	XP_016867976.1:p.Met4378Val
XM_017012488.1:c.13096A>G	XP_016867977.1:p.Met4366Val
XM_017012489.1:c.9949A>G	XP_016867978.1:p.Met3317Val
XM_017012490.2:c.9553A>G	XP_016867979.1:p.Met3185Val
XM_024446852.1:c.13276A>G	XP_024302620.1:p.Met4426Val
XM_024446853.1:c.13204A>G	XP_024302621.1:p.Met4402Val
NM_170606.3:c.13063A>G MANE Select	NP_733751.2:p.Met4355Val