Canonical Allele Identifier: CA1752986454
Gene: KMT2C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152148859T= , CM000669.2:g.152148859T= GRCh38
NC_000007.13:g.151845944T= , CM000669.1:g.151845944T= GRCh37
NC_000007.12:g.151476877T= NCBI36
NG_033948.1:g.292147A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682040.1:c.1256A=
ENST00000682116.1:n.2200A=
ENST00000682283.1:c.13239A= ENSP00000507485.1:p.Lys4413=
ENST00000682629.1:n.2368A=
ENST00000683120.1:n.8260A=
ENST00000683178.1:c.3641A=
ENST00000683200.1:c.10578A= ENSP00000508052.1:p.Lys3526=
ENST00000683337.1:n.4698A=
ENST00000683502.1:c.3713A=
ENST00000683621.1:n.1834A=
ENST00000683640.1:n.1784A=
ENST00000684069.1:c.1485A= ENSP00000507650.1:p.Lys495=
ENST00000684261.1:c.7965A= ENSP00000508097.1:p.Lys2655=
ENST00000684649.1:c.3713A=
ENST00000262189.11:c.13068A= MANE Select ENSP00000262189.6:p.Lys4356=
ENST00000360104.8:c.8855A=
ENST00000418061.2:c.3710A=
ENST00000424877.6:c.3644A=
ENST00000679393.1:n.7779A=
ENST00000679560.1:c.7968A= ENSP00000505094.1:p.Lys2656=
ENST00000679882.1:c.12633A= ENSP00000506154.1:p.Lys4211=
ENST00000680029.1:c.3645A=
ENST00000680877.1:c.7968A= ENSP00000505724.1:p.Lys2656=
ENST00000681923.1:n.2083A=
ENST00000262189.10:c.13068A= ENSP00000262189.6:p.Lys4356=
ENST00000355193.6:c.13068A= ENSP00000347325.3:p.Lys4356=
ENST00000360104.7:c.5749A=
ENST00000424877.5:c.2919A= ENSP00000410411.1:p.Lys973=
ENST00000473186.5:n.10950A=
ENST00000558084.5:c.*10588A= ENSP00000453752.1:n.*10588A=
NM_170606.2:c.13068A= NP_733751.2:p.Lys4356=
XM_005250025.3:c.13284A= XP_005250082.1:p.Lys4428=
XM_005250026.2:c.13281A= XP_005250083.1:p.Lys4427=
XM_005250027.3:c.13281A= XP_005250084.1:p.Lys4427=
XM_005250028.3:c.13284A= XP_005250085.1:p.Lys4428=
XM_005250031.3:c.13119A= XP_005250088.1:p.Lys4373=
XM_006716077.2:c.13281A= XP_006716140.1:p.Lys4427=
XM_006716078.2:c.13212A= XP_006716141.1:p.Lys4404=
XM_006716079.2:c.13116A= XP_006716142.1:p.Lys4372=
XM_011516450.1:c.13236A= XP_011514752.1:p.Lys4412=
XM_011516451.1:c.13164A= XP_011514753.1:p.Lys4388=
XM_011516452.1:c.13131A= XP_011514754.1:p.Lys4377=
XM_011516453.1:c.13047A= XP_011514755.1:p.Lys4349=
XM_011516454.1:c.12369A= XP_011514756.1:p.Lys4123=
XM_011516455.1:c.10830A= XP_011514757.1:p.Lys3610=
XM_011516456.1:c.13236A= XP_011514758.1:p.Lys4412=
XM_005250025.4:c.13284A= XP_005250082.1:p.Lys4428=
XM_005250026.3:c.13281A= XP_005250083.1:p.Lys4427=
XM_005250027.4:c.13281A= XP_005250084.1:p.Lys4427=
XM_005250028.4:c.13284A= XP_005250085.1:p.Lys4428=
XM_005250031.4:c.13119A= XP_005250088.1:p.Lys4373=
XM_006716077.3:c.13281A= XP_006716140.1:p.Lys4427=
XM_006716078.3:c.13212A= XP_006716141.1:p.Lys4404=
XM_006716079.3:c.13116A= XP_006716142.1:p.Lys4372=
XM_011516450.2:c.13236A= XP_011514752.1:p.Lys4412=
XM_011516451.2:c.13164A= XP_011514753.1:p.Lys4388=
XM_011516452.2:c.13131A= XP_011514754.1:p.Lys4377=
XM_011516453.2:c.13047A= XP_011514755.1:p.Lys4349=
XM_011516454.2:c.12369A= XP_011514756.1:p.Lys4123=
XM_011516456.2:c.13236A= XP_011514758.1:p.Lys4412=
XM_017012480.1:c.13284A= XP_016867969.1:p.Lys4428=
XM_017012481.1:c.13281A= XP_016867970.1:p.Lys4427=
XM_017012482.1:c.13281A= XP_016867971.1:p.Lys4427=
XM_017012483.1:c.13281A= XP_016867972.1:p.Lys4427=
XM_017012484.1:c.13251A= XP_016867973.1:p.Lys4417=
XM_017012485.1:c.13233A= XP_016867974.1:p.Lys4411=
XM_017012486.1:c.13209A= XP_016867975.1:p.Lys4403=
XM_017012487.1:c.13137A= XP_016867976.1:p.Lys4379=
XM_017012488.1:c.13101A= XP_016867977.1:p.Lys4367=
XM_017012489.1:c.9954A= XP_016867978.1:p.Lys3318=
XM_017012490.2:c.9558A= XP_016867979.1:p.Lys3186=
XM_024446852.1:c.13281A= XP_024302620.1:p.Lys4427=
XM_024446853.1:c.13209A= XP_024302621.1:p.Lys4403=
NM_170606.3:c.13068A= MANE Select NP_733751.2:p.Lys4356=