Canonical Allele Identifier: CA458884651

Gene: KMT2C

Linked Data

• dbSNP Id: rs2129095516
• MyVariant Identifiers: chr7:g.151845827C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148742C>A , CM000669.2:g.152148742C>A	GRCh38
NC_000007.13:g.151845827C>A , CM000669.1:g.151845827C>A	GRCh37
NC_000007.12:g.151476760C>A	NCBI36
NG_033948.1:g.292264G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1373G>T
ENST00000682116.1:n.2317G>T
ENST00000682283.1:c.13356G>T	ENSP00000507485.1:p.Val4452=
ENST00000682629.1:n.2485G>T
ENST00000683120.1:n.8377G>T
ENST00000683178.1:c.3758G>T
ENST00000683200.1:c.10695G>T	ENSP00000508052.1:p.Val3565=
ENST00000683337.1:n.4815G>T
ENST00000683502.1:c.3830G>T
ENST00000683621.1:n.1951G>T
ENST00000683640.1:n.1901G>T
ENST00000684069.1:c.1602G>T	ENSP00000507650.1:p.Val534=
ENST00000684261.1:c.8082G>T	ENSP00000508097.1:p.Val2694=
ENST00000684649.1:c.3830G>T
ENST00000262189.11:c.13185G>T MANE Select	ENSP00000262189.6:p.Val4395=
ENST00000360104.8:c.8972G>T
ENST00000418061.2:c.3827G>T
ENST00000424877.6:c.3761G>T
ENST00000679393.1:n.7896G>T
ENST00000679560.1:c.8085G>T	ENSP00000505094.1:p.Val2695=
ENST00000679882.1:c.12750G>T	ENSP00000506154.1:p.Val4250=
ENST00000680029.1:c.3762G>T
ENST00000680877.1:c.8085G>T	ENSP00000505724.1:p.Val2695=
ENST00000681923.1:n.2200G>T
ENST00000262189.10:c.13185G>T	ENSP00000262189.6:p.Val4395=
ENST00000355193.6:c.13185G>T	ENSP00000347325.3:p.Val4395=
ENST00000360104.7:c.5866G>T
ENST00000424877.5:c.3036G>T	ENSP00000410411.1:p.Val1012=
ENST00000473186.5:n.11067G>T
ENST00000558084.5:c.*10705G>T	ENSP00000453752.1:n.*10705G>T
NM_170606.2:c.13185G>T	NP_733751.2:p.Val4395=
XM_005250025.3:c.13401G>T	XP_005250082.1:p.Val4467=
XM_005250026.2:c.13398G>T	XP_005250083.1:p.Val4466=
XM_005250027.3:c.13398G>T	XP_005250084.1:p.Val4466=
XM_005250028.3:c.13401G>T	XP_005250085.1:p.Val4467=
XM_005250031.3:c.13236G>T	XP_005250088.1:p.Val4412=
XM_006716077.2:c.13398G>T	XP_006716140.1:p.Val4466=
XM_006716078.2:c.13329G>T	XP_006716141.1:p.Val4443=
XM_006716079.2:c.13233G>T	XP_006716142.1:p.Val4411=
XM_011516450.1:c.13353G>T	XP_011514752.1:p.Val4451=
XM_011516451.1:c.13281G>T	XP_011514753.1:p.Val4427=
XM_011516452.1:c.13248G>T	XP_011514754.1:p.Val4416=
XM_011516453.1:c.13164G>T	XP_011514755.1:p.Val4388=
XM_011516454.1:c.12486G>T	XP_011514756.1:p.Val4162=
XM_011516455.1:c.10947G>T	XP_011514757.1:p.Val3649=
XM_011516456.1:c.13353G>T	XP_011514758.1:p.Val4451=
XM_005250025.4:c.13401G>T	XP_005250082.1:p.Val4467=
XM_005250026.3:c.13398G>T	XP_005250083.1:p.Val4466=
XM_005250027.4:c.13398G>T	XP_005250084.1:p.Val4466=
XM_005250028.4:c.13401G>T	XP_005250085.1:p.Val4467=
XM_005250031.4:c.13236G>T	XP_005250088.1:p.Val4412=
XM_006716077.3:c.13398G>T	XP_006716140.1:p.Val4466=
XM_006716078.3:c.13329G>T	XP_006716141.1:p.Val4443=
XM_006716079.3:c.13233G>T	XP_006716142.1:p.Val4411=
XM_011516450.2:c.13353G>T	XP_011514752.1:p.Val4451=
XM_011516451.2:c.13281G>T	XP_011514753.1:p.Val4427=
XM_011516452.2:c.13248G>T	XP_011514754.1:p.Val4416=
XM_011516453.2:c.13164G>T	XP_011514755.1:p.Val4388=
XM_011516454.2:c.12486G>T	XP_011514756.1:p.Val4162=
XM_011516456.2:c.13353G>T	XP_011514758.1:p.Val4451=
XM_017012480.1:c.13401G>T	XP_016867969.1:p.Val4467=
XM_017012481.1:c.13398G>T	XP_016867970.1:p.Val4466=
XM_017012482.1:c.13398G>T	XP_016867971.1:p.Val4466=
XM_017012483.1:c.13398G>T	XP_016867972.1:p.Val4466=
XM_017012484.1:c.13368G>T	XP_016867973.1:p.Val4456=
XM_017012485.1:c.13350G>T	XP_016867974.1:p.Val4450=
XM_017012486.1:c.13326G>T	XP_016867975.1:p.Val4442=
XM_017012487.1:c.13254G>T	XP_016867976.1:p.Val4418=
XM_017012488.1:c.13218G>T	XP_016867977.1:p.Val4406=
XM_017012489.1:c.10071G>T	XP_016867978.1:p.Val3357=
XM_017012490.2:c.9675G>T	XP_016867979.1:p.Val3225=
XM_024446852.1:c.13398G>T	XP_024302620.1:p.Val4466=
XM_024446853.1:c.13326G>T	XP_024302621.1:p.Val4442=
NM_170606.3:c.13185G>T MANE Select	NP_733751.2:p.Val4395=