Canonical Allele Identifier: CA458884714

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845875T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148790T>A , CM000669.2:g.152148790T>A	GRCh38
NC_000007.13:g.151845875T>A , CM000669.1:g.151845875T>A	GRCh37
NC_000007.12:g.151476808T>A	NCBI36
NG_033948.1:g.292216A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1325A>T
ENST00000682116.1:n.2269A>T
ENST00000682283.1:c.13308A>T	ENSP00000507485.1:p.Ile4436=
ENST00000682629.1:n.2437A>T
ENST00000683120.1:n.8329A>T
ENST00000683178.1:c.3710A>T
ENST00000683200.1:c.10647A>T	ENSP00000508052.1:p.Ile3549=
ENST00000683337.1:n.4767A>T
ENST00000683502.1:c.3782A>T
ENST00000683621.1:n.1903A>T
ENST00000683640.1:n.1853A>T
ENST00000684069.1:c.1554A>T	ENSP00000507650.1:p.Ile518=
ENST00000684261.1:c.8034A>T	ENSP00000508097.1:p.Ile2678=
ENST00000684649.1:c.3782A>T
ENST00000262189.11:c.13137A>T MANE Select	ENSP00000262189.6:p.Ile4379=
ENST00000360104.8:c.8924A>T
ENST00000418061.2:c.3779A>T
ENST00000424877.6:c.3713A>T
ENST00000679393.1:n.7848A>T
ENST00000679560.1:c.8037A>T	ENSP00000505094.1:p.Ile2679=
ENST00000679882.1:c.12702A>T	ENSP00000506154.1:p.Ile4234=
ENST00000680029.1:c.3714A>T
ENST00000680877.1:c.8037A>T	ENSP00000505724.1:p.Ile2679=
ENST00000681923.1:n.2152A>T
ENST00000262189.10:c.13137A>T	ENSP00000262189.6:p.Ile4379=
ENST00000355193.6:c.13137A>T	ENSP00000347325.3:p.Ile4379=
ENST00000360104.7:c.5818A>T
ENST00000424877.5:c.2988A>T	ENSP00000410411.1:p.Ile996=
ENST00000473186.5:n.11019A>T
ENST00000558084.5:c.*10657A>T	ENSP00000453752.1:n.*10657A>T
NM_170606.2:c.13137A>T	NP_733751.2:p.Ile4379=
XM_005250025.3:c.13353A>T	XP_005250082.1:p.Ile4451=
XM_005250026.2:c.13350A>T	XP_005250083.1:p.Ile4450=
XM_005250027.3:c.13350A>T	XP_005250084.1:p.Ile4450=
XM_005250028.3:c.13353A>T	XP_005250085.1:p.Ile4451=
XM_005250031.3:c.13188A>T	XP_005250088.1:p.Ile4396=
XM_006716077.2:c.13350A>T	XP_006716140.1:p.Ile4450=
XM_006716078.2:c.13281A>T	XP_006716141.1:p.Ile4427=
XM_006716079.2:c.13185A>T	XP_006716142.1:p.Ile4395=
XM_011516450.1:c.13305A>T	XP_011514752.1:p.Ile4435=
XM_011516451.1:c.13233A>T	XP_011514753.1:p.Ile4411=
XM_011516452.1:c.13200A>T	XP_011514754.1:p.Ile4400=
XM_011516453.1:c.13116A>T	XP_011514755.1:p.Ile4372=
XM_011516454.1:c.12438A>T	XP_011514756.1:p.Ile4146=
XM_011516455.1:c.10899A>T	XP_011514757.1:p.Ile3633=
XM_011516456.1:c.13305A>T	XP_011514758.1:p.Ile4435=
XM_005250025.4:c.13353A>T	XP_005250082.1:p.Ile4451=
XM_005250026.3:c.13350A>T	XP_005250083.1:p.Ile4450=
XM_005250027.4:c.13350A>T	XP_005250084.1:p.Ile4450=
XM_005250028.4:c.13353A>T	XP_005250085.1:p.Ile4451=
XM_005250031.4:c.13188A>T	XP_005250088.1:p.Ile4396=
XM_006716077.3:c.13350A>T	XP_006716140.1:p.Ile4450=
XM_006716078.3:c.13281A>T	XP_006716141.1:p.Ile4427=
XM_006716079.3:c.13185A>T	XP_006716142.1:p.Ile4395=
XM_011516450.2:c.13305A>T	XP_011514752.1:p.Ile4435=
XM_011516451.2:c.13233A>T	XP_011514753.1:p.Ile4411=
XM_011516452.2:c.13200A>T	XP_011514754.1:p.Ile4400=
XM_011516453.2:c.13116A>T	XP_011514755.1:p.Ile4372=
XM_011516454.2:c.12438A>T	XP_011514756.1:p.Ile4146=
XM_011516456.2:c.13305A>T	XP_011514758.1:p.Ile4435=
XM_017012480.1:c.13353A>T	XP_016867969.1:p.Ile4451=
XM_017012481.1:c.13350A>T	XP_016867970.1:p.Ile4450=
XM_017012482.1:c.13350A>T	XP_016867971.1:p.Ile4450=
XM_017012483.1:c.13350A>T	XP_016867972.1:p.Ile4450=
XM_017012484.1:c.13320A>T	XP_016867973.1:p.Ile4440=
XM_017012485.1:c.13302A>T	XP_016867974.1:p.Ile4434=
XM_017012486.1:c.13278A>T	XP_016867975.1:p.Ile4426=
XM_017012487.1:c.13206A>T	XP_016867976.1:p.Ile4402=
XM_017012488.1:c.13170A>T	XP_016867977.1:p.Ile4390=
XM_017012489.1:c.10023A>T	XP_016867978.1:p.Ile3341=
XM_017012490.2:c.9627A>T	XP_016867979.1:p.Ile3209=
XM_024446852.1:c.13350A>T	XP_024302620.1:p.Ile4450=
XM_024446853.1:c.13278A>T	XP_024302621.1:p.Ile4426=
NM_170606.3:c.13137A>T MANE Select	NP_733751.2:p.Ile4379=