Canonical Allele Identifier: CA458884657

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845830A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148745A>T , CM000669.2:g.152148745A>T	GRCh38
NC_000007.13:g.151845830A>T , CM000669.1:g.151845830A>T	GRCh37
NC_000007.12:g.151476763A>T	NCBI36
NG_033948.1:g.292261T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1370T>A
ENST00000682116.1:n.2314T>A
ENST00000682283.1:c.13353T>A	ENSP00000507485.1:p.Pro4451=
ENST00000682629.1:n.2482T>A
ENST00000683120.1:n.8374T>A
ENST00000683178.1:c.3755T>A
ENST00000683200.1:c.10692T>A	ENSP00000508052.1:p.Pro3564=
ENST00000683337.1:n.4812T>A
ENST00000683502.1:c.3827T>A
ENST00000683621.1:n.1948T>A
ENST00000683640.1:n.1898T>A
ENST00000684069.1:c.1599T>A	ENSP00000507650.1:p.Pro533=
ENST00000684261.1:c.8079T>A	ENSP00000508097.1:p.Pro2693=
ENST00000684649.1:c.3827T>A
ENST00000262189.11:c.13182T>A MANE Select	ENSP00000262189.6:p.Pro4394=
ENST00000360104.8:c.8969T>A
ENST00000418061.2:c.3824T>A
ENST00000424877.6:c.3758T>A
ENST00000679393.1:n.7893T>A
ENST00000679560.1:c.8082T>A	ENSP00000505094.1:p.Pro2694=
ENST00000679882.1:c.12747T>A	ENSP00000506154.1:p.Pro4249=
ENST00000680029.1:c.3759T>A
ENST00000680877.1:c.8082T>A	ENSP00000505724.1:p.Pro2694=
ENST00000681923.1:n.2197T>A
ENST00000262189.10:c.13182T>A	ENSP00000262189.6:p.Pro4394=
ENST00000355193.6:c.13182T>A	ENSP00000347325.3:p.Pro4394=
ENST00000360104.7:c.5863T>A
ENST00000424877.5:c.3033T>A	ENSP00000410411.1:p.Pro1011=
ENST00000473186.5:n.11064T>A
ENST00000558084.5:c.*10702T>A	ENSP00000453752.1:n.*10702T>A
NM_170606.2:c.13182T>A	NP_733751.2:p.Pro4394=
XM_005250025.3:c.13398T>A	XP_005250082.1:p.Pro4466=
XM_005250026.2:c.13395T>A	XP_005250083.1:p.Pro4465=
XM_005250027.3:c.13395T>A	XP_005250084.1:p.Pro4465=
XM_005250028.3:c.13398T>A	XP_005250085.1:p.Pro4466=
XM_005250031.3:c.13233T>A	XP_005250088.1:p.Pro4411=
XM_006716077.2:c.13395T>A	XP_006716140.1:p.Pro4465=
XM_006716078.2:c.13326T>A	XP_006716141.1:p.Pro4442=
XM_006716079.2:c.13230T>A	XP_006716142.1:p.Pro4410=
XM_011516450.1:c.13350T>A	XP_011514752.1:p.Pro4450=
XM_011516451.1:c.13278T>A	XP_011514753.1:p.Pro4426=
XM_011516452.1:c.13245T>A	XP_011514754.1:p.Pro4415=
XM_011516453.1:c.13161T>A	XP_011514755.1:p.Pro4387=
XM_011516454.1:c.12483T>A	XP_011514756.1:p.Pro4161=
XM_011516455.1:c.10944T>A	XP_011514757.1:p.Pro3648=
XM_011516456.1:c.13350T>A	XP_011514758.1:p.Pro4450=
XM_005250025.4:c.13398T>A	XP_005250082.1:p.Pro4466=
XM_005250026.3:c.13395T>A	XP_005250083.1:p.Pro4465=
XM_005250027.4:c.13395T>A	XP_005250084.1:p.Pro4465=
XM_005250028.4:c.13398T>A	XP_005250085.1:p.Pro4466=
XM_005250031.4:c.13233T>A	XP_005250088.1:p.Pro4411=
XM_006716077.3:c.13395T>A	XP_006716140.1:p.Pro4465=
XM_006716078.3:c.13326T>A	XP_006716141.1:p.Pro4442=
XM_006716079.3:c.13230T>A	XP_006716142.1:p.Pro4410=
XM_011516450.2:c.13350T>A	XP_011514752.1:p.Pro4450=
XM_011516451.2:c.13278T>A	XP_011514753.1:p.Pro4426=
XM_011516452.2:c.13245T>A	XP_011514754.1:p.Pro4415=
XM_011516453.2:c.13161T>A	XP_011514755.1:p.Pro4387=
XM_011516454.2:c.12483T>A	XP_011514756.1:p.Pro4161=
XM_011516456.2:c.13350T>A	XP_011514758.1:p.Pro4450=
XM_017012480.1:c.13398T>A	XP_016867969.1:p.Pro4466=
XM_017012481.1:c.13395T>A	XP_016867970.1:p.Pro4465=
XM_017012482.1:c.13395T>A	XP_016867971.1:p.Pro4465=
XM_017012483.1:c.13395T>A	XP_016867972.1:p.Pro4465=
XM_017012484.1:c.13365T>A	XP_016867973.1:p.Pro4455=
XM_017012485.1:c.13347T>A	XP_016867974.1:p.Pro4449=
XM_017012486.1:c.13323T>A	XP_016867975.1:p.Pro4441=
XM_017012487.1:c.13251T>A	XP_016867976.1:p.Pro4417=
XM_017012488.1:c.13215T>A	XP_016867977.1:p.Pro4405=
XM_017012489.1:c.10068T>A	XP_016867978.1:p.Pro3356=
XM_017012490.2:c.9672T>A	XP_016867979.1:p.Pro3224=
XM_024446852.1:c.13395T>A	XP_024302620.1:p.Pro4465=
XM_024446853.1:c.13323T>A	XP_024302621.1:p.Pro4441=
NM_170606.3:c.13182T>A MANE Select	NP_733751.2:p.Pro4394=