Canonical Allele Identifier: CA645565077
Gene: KMT2C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152148827_152148828delinsAA , CM000669.2:g.152148827_152148828delinsAA GRCh38
NC_000007.13:g.151845912_151845913delinsAA , CM000669.1:g.151845912_151845913delinsAA GRCh37
NC_000007.12:g.151476845_151476846delinsAA NCBI36
NG_033948.1:g.292178_292179delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000682040.1:c.1287_1288delinsTT
ENST00000682116.1:n.2231_2232delinsTT
ENST00000682283.1:c.13270_13271delinsTT ENSP00000507485.1:p.Pro4424Phe
ENST00000682629.1:n.2399_2400delinsTT
ENST00000683120.1:n.8291_8292delinsTT
ENST00000683178.1:c.3672_3673delinsTT
ENST00000683200.1:c.10609_10610delinsTT ENSP00000508052.1:p.Pro3537Phe
ENST00000683337.1:n.4729_4730delinsTT
ENST00000683502.1:c.3744_3745delinsTT
ENST00000683621.1:n.1865_1866delinsTT
ENST00000683640.1:n.1815_1816delinsTT
ENST00000684069.1:c.1516_1517delinsTT ENSP00000507650.1:p.Pro506Phe
ENST00000684261.1:c.7996_7997delinsTT ENSP00000508097.1:p.Pro2666Phe
ENST00000684649.1:c.3744_3745delinsTT
ENST00000262189.11:c.13099_13100delinsTT MANE Select ENSP00000262189.6:p.Pro4367Phe
ENST00000360104.8:c.8886_8887delinsTT
ENST00000418061.2:c.3741_3742delinsTT
ENST00000424877.6:c.3675_3676delinsTT
ENST00000679393.1:n.7810_7811delinsTT
ENST00000679560.1:c.7999_8000delinsTT ENSP00000505094.1:p.Pro2667Phe
ENST00000679882.1:c.12664_12665delinsTT ENSP00000506154.1:p.Pro4222Phe
ENST00000680029.1:c.3676_3677delinsTT
ENST00000680877.1:c.7999_8000delinsTT ENSP00000505724.1:p.Pro2667Phe
ENST00000681923.1:n.2114_2115delinsTT
ENST00000262189.10:c.13099_13100delinsTT ENSP00000262189.6:p.Pro4367Phe
ENST00000355193.6:c.13099_13100delinsTT ENSP00000347325.3:p.Pro4367Phe
ENST00000360104.7:c.5780_5781delinsTT
ENST00000424877.5:c.2950_2951delinsTT ENSP00000410411.1:p.Pro984Phe
ENST00000473186.5:n.10981_10982delinsTT
ENST00000558084.5:c.*10619_*10620delinsTT ENSP00000453752.1:n.*10619_*10620delinsTT
NM_170606.2:c.13099_13100delinsTT NP_733751.2:p.Pro4367Phe
XM_005250025.3:c.13315_13316delinsTT XP_005250082.1:p.Pro4439Phe
XM_005250026.2:c.13312_13313delinsTT XP_005250083.1:p.Pro4438Phe
XM_005250027.3:c.13312_13313delinsTT XP_005250084.1:p.Pro4438Phe
XM_005250028.3:c.13315_13316delinsTT XP_005250085.1:p.Pro4439Phe
XM_005250031.3:c.13150_13151delinsTT XP_005250088.1:p.Pro4384Phe
XM_006716077.2:c.13312_13313delinsTT XP_006716140.1:p.Pro4438Phe
XM_006716078.2:c.13243_13244delinsTT XP_006716141.1:p.Pro4415Phe
XM_006716079.2:c.13147_13148delinsTT XP_006716142.1:p.Pro4383Phe
XM_011516450.1:c.13267_13268delinsTT XP_011514752.1:p.Pro4423Phe
XM_011516451.1:c.13195_13196delinsTT XP_011514753.1:p.Pro4399Phe
XM_011516452.1:c.13162_13163delinsTT XP_011514754.1:p.Pro4388Phe
XM_011516453.1:c.13078_13079delinsTT XP_011514755.1:p.Pro4360Phe
XM_011516454.1:c.12400_12401delinsTT XP_011514756.1:p.Pro4134Phe
XM_011516455.1:c.10861_10862delinsTT XP_011514757.1:p.Pro3621Phe
XM_011516456.1:c.13267_13268delinsTT XP_011514758.1:p.Pro4423Phe
XM_005250025.4:c.13315_13316delinsTT XP_005250082.1:p.Pro4439Phe
XM_005250026.3:c.13312_13313delinsTT XP_005250083.1:p.Pro4438Phe
XM_005250027.4:c.13312_13313delinsTT XP_005250084.1:p.Pro4438Phe
XM_005250028.4:c.13315_13316delinsTT XP_005250085.1:p.Pro4439Phe
XM_005250031.4:c.13150_13151delinsTT XP_005250088.1:p.Pro4384Phe
XM_006716077.3:c.13312_13313delinsTT XP_006716140.1:p.Pro4438Phe
XM_006716078.3:c.13243_13244delinsTT XP_006716141.1:p.Pro4415Phe
XM_006716079.3:c.13147_13148delinsTT XP_006716142.1:p.Pro4383Phe
XM_011516450.2:c.13267_13268delinsTT XP_011514752.1:p.Pro4423Phe
XM_011516451.2:c.13195_13196delinsTT XP_011514753.1:p.Pro4399Phe
XM_011516452.2:c.13162_13163delinsTT XP_011514754.1:p.Pro4388Phe
XM_011516453.2:c.13078_13079delinsTT XP_011514755.1:p.Pro4360Phe
XM_011516454.2:c.12400_12401delinsTT XP_011514756.1:p.Pro4134Phe
XM_011516456.2:c.13267_13268delinsTT XP_011514758.1:p.Pro4423Phe
XM_017012480.1:c.13315_13316delinsTT XP_016867969.1:p.Pro4439Phe
XM_017012481.1:c.13312_13313delinsTT XP_016867970.1:p.Pro4438Phe
XM_017012482.1:c.13312_13313delinsTT XP_016867971.1:p.Pro4438Phe
XM_017012483.1:c.13312_13313delinsTT XP_016867972.1:p.Pro4438Phe
XM_017012484.1:c.13282_13283delinsTT XP_016867973.1:p.Pro4428Phe
XM_017012485.1:c.13264_13265delinsTT XP_016867974.1:p.Pro4422Phe
XM_017012486.1:c.13240_13241delinsTT XP_016867975.1:p.Pro4414Phe
XM_017012487.1:c.13168_13169delinsTT XP_016867976.1:p.Pro4390Phe
XM_017012488.1:c.13132_13133delinsTT XP_016867977.1:p.Pro4378Phe
XM_017012489.1:c.9985_9986delinsTT XP_016867978.1:p.Pro3329Phe
XM_017012490.2:c.9589_9590delinsTT XP_016867979.1:p.Pro3197Phe
XM_024446852.1:c.13312_13313delinsTT XP_024302620.1:p.Pro4438Phe
XM_024446853.1:c.13240_13241delinsTT XP_024302621.1:p.Pro4414Phe
NM_170606.3:c.13099_13100delinsTT MANE Select NP_733751.2:p.Pro4367Phe