Canonical Allele Identifier: CA1752986493
Gene: KMT2C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152148881T= , CM000669.2:g.152148881T= GRCh38
NC_000007.13:g.151845966T= , CM000669.1:g.151845966T= GRCh37
NC_000007.12:g.151476899T= NCBI36
NG_033948.1:g.292125A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682040.1:c.1234A=
ENST00000682116.1:n.2178A=
ENST00000682283.1:c.13217A= ENSP00000507485.1:p.Asn4406=
ENST00000682629.1:n.2346A=
ENST00000683120.1:n.8238A=
ENST00000683178.1:c.3619A=
ENST00000683200.1:c.10556A= ENSP00000508052.1:p.Asn3519=
ENST00000683337.1:n.4676A=
ENST00000683502.1:c.3691A=
ENST00000683621.1:n.1812A=
ENST00000683640.1:n.1762A=
ENST00000684069.1:c.1463A= ENSP00000507650.1:p.Asn488=
ENST00000684261.1:c.7943A= ENSP00000508097.1:p.Asn2648=
ENST00000684649.1:c.3691A=
ENST00000262189.11:c.13046A= MANE Select ENSP00000262189.6:p.Asn4349=
ENST00000360104.8:c.8833A=
ENST00000418061.2:c.3688A=
ENST00000424877.6:c.3622A=
ENST00000679393.1:n.7757A=
ENST00000679560.1:c.7946A= ENSP00000505094.1:p.Asn2649=
ENST00000679882.1:c.12611A= ENSP00000506154.1:p.Asn4204=
ENST00000680029.1:c.3623A=
ENST00000680877.1:c.7946A= ENSP00000505724.1:p.Asn2649=
ENST00000681923.1:n.2061A=
ENST00000262189.10:c.13046A= ENSP00000262189.6:p.Asn4349=
ENST00000355193.6:c.13046A= ENSP00000347325.3:p.Asn4349=
ENST00000360104.7:c.5727A=
ENST00000424877.5:c.2897A= ENSP00000410411.1:p.Asn966=
ENST00000473186.5:n.10928A=
ENST00000558084.5:c.*10566A= ENSP00000453752.1:n.*10566A=
NM_170606.2:c.13046A= NP_733751.2:p.Asn4349=
XM_005250025.3:c.13262A= XP_005250082.1:p.Asn4421=
XM_005250026.2:c.13259A= XP_005250083.1:p.Asn4420=
XM_005250027.3:c.13259A= XP_005250084.1:p.Asn4420=
XM_005250028.3:c.13262A= XP_005250085.1:p.Asn4421=
XM_005250031.3:c.13097A= XP_005250088.1:p.Asn4366=
XM_006716077.2:c.13259A= XP_006716140.1:p.Asn4420=
XM_006716078.2:c.13190A= XP_006716141.1:p.Asn4397=
XM_006716079.2:c.13094A= XP_006716142.1:p.Asn4365=
XM_011516450.1:c.13214A= XP_011514752.1:p.Asn4405=
XM_011516451.1:c.13142A= XP_011514753.1:p.Asn4381=
XM_011516452.1:c.13109A= XP_011514754.1:p.Asn4370=
XM_011516453.1:c.13025A= XP_011514755.1:p.Asn4342=
XM_011516454.1:c.12347A= XP_011514756.1:p.Asn4116=
XM_011516455.1:c.10808A= XP_011514757.1:p.Asn3603=
XM_011516456.1:c.13214A= XP_011514758.1:p.Asn4405=
XM_005250025.4:c.13262A= XP_005250082.1:p.Asn4421=
XM_005250026.3:c.13259A= XP_005250083.1:p.Asn4420=
XM_005250027.4:c.13259A= XP_005250084.1:p.Asn4420=
XM_005250028.4:c.13262A= XP_005250085.1:p.Asn4421=
XM_005250031.4:c.13097A= XP_005250088.1:p.Asn4366=
XM_006716077.3:c.13259A= XP_006716140.1:p.Asn4420=
XM_006716078.3:c.13190A= XP_006716141.1:p.Asn4397=
XM_006716079.3:c.13094A= XP_006716142.1:p.Asn4365=
XM_011516450.2:c.13214A= XP_011514752.1:p.Asn4405=
XM_011516451.2:c.13142A= XP_011514753.1:p.Asn4381=
XM_011516452.2:c.13109A= XP_011514754.1:p.Asn4370=
XM_011516453.2:c.13025A= XP_011514755.1:p.Asn4342=
XM_011516454.2:c.12347A= XP_011514756.1:p.Asn4116=
XM_011516456.2:c.13214A= XP_011514758.1:p.Asn4405=
XM_017012480.1:c.13262A= XP_016867969.1:p.Asn4421=
XM_017012481.1:c.13259A= XP_016867970.1:p.Asn4420=
XM_017012482.1:c.13259A= XP_016867971.1:p.Asn4420=
XM_017012483.1:c.13259A= XP_016867972.1:p.Asn4420=
XM_017012484.1:c.13229A= XP_016867973.1:p.Asn4410=
XM_017012485.1:c.13211A= XP_016867974.1:p.Asn4404=
XM_017012486.1:c.13187A= XP_016867975.1:p.Asn4396=
XM_017012487.1:c.13115A= XP_016867976.1:p.Asn4372=
XM_017012488.1:c.13079A= XP_016867977.1:p.Asn4360=
XM_017012489.1:c.9932A= XP_016867978.1:p.Asn3311=
XM_017012490.2:c.9536A= XP_016867979.1:p.Asn3179=
XM_024446852.1:c.13259A= XP_024302620.1:p.Asn4420=
XM_024446853.1:c.13187A= XP_024302621.1:p.Asn4396=
NM_170606.3:c.13046A= MANE Select NP_733751.2:p.Asn4349=