Canonical Allele Identifier: CA458884960

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845968G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148883G>C , CM000669.2:g.152148883G>C	GRCh38
NC_000007.13:g.151845968G>C , CM000669.1:g.151845968G>C	GRCh37
NC_000007.12:g.151476901G>C	NCBI36
NG_033948.1:g.292123C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1232C>G
ENST00000682116.1:n.2176C>G
ENST00000682283.1:c.13215C>G	ENSP00000507485.1:p.Leu4405=
ENST00000682629.1:n.2344C>G
ENST00000683120.1:n.8236C>G
ENST00000683178.1:c.3617C>G
ENST00000683200.1:c.10554C>G	ENSP00000508052.1:p.Leu3518=
ENST00000683337.1:n.4674C>G
ENST00000683502.1:c.3689C>G
ENST00000683621.1:n.1810C>G
ENST00000683640.1:n.1760C>G
ENST00000684069.1:c.1461C>G	ENSP00000507650.1:p.Leu487=
ENST00000684261.1:c.7941C>G	ENSP00000508097.1:p.Leu2647=
ENST00000684649.1:c.3689C>G
ENST00000262189.11:c.13044C>G MANE Select	ENSP00000262189.6:p.Leu4348=
ENST00000360104.8:c.8831C>G
ENST00000418061.2:c.3686C>G
ENST00000424877.6:c.3620C>G
ENST00000679393.1:n.7755C>G
ENST00000679560.1:c.7944C>G	ENSP00000505094.1:p.Leu2648=
ENST00000679882.1:c.12609C>G	ENSP00000506154.1:p.Leu4203=
ENST00000680029.1:c.3621C>G
ENST00000680877.1:c.7944C>G	ENSP00000505724.1:p.Leu2648=
ENST00000681923.1:n.2059C>G
ENST00000262189.10:c.13044C>G	ENSP00000262189.6:p.Leu4348=
ENST00000355193.6:c.13044C>G	ENSP00000347325.3:p.Leu4348=
ENST00000360104.7:c.5725C>G
ENST00000424877.5:c.2895C>G	ENSP00000410411.1:p.Leu965=
ENST00000473186.5:n.10926C>G
ENST00000558084.5:c.*10564C>G	ENSP00000453752.1:n.*10564C>G
NM_170606.2:c.13044C>G	NP_733751.2:p.Leu4348=
XM_005250025.3:c.13260C>G	XP_005250082.1:p.Leu4420=
XM_005250026.2:c.13257C>G	XP_005250083.1:p.Leu4419=
XM_005250027.3:c.13257C>G	XP_005250084.1:p.Leu4419=
XM_005250028.3:c.13260C>G	XP_005250085.1:p.Leu4420=
XM_005250031.3:c.13095C>G	XP_005250088.1:p.Leu4365=
XM_006716077.2:c.13257C>G	XP_006716140.1:p.Leu4419=
XM_006716078.2:c.13188C>G	XP_006716141.1:p.Leu4396=
XM_006716079.2:c.13092C>G	XP_006716142.1:p.Leu4364=
XM_011516450.1:c.13212C>G	XP_011514752.1:p.Leu4404=
XM_011516451.1:c.13140C>G	XP_011514753.1:p.Leu4380=
XM_011516452.1:c.13107C>G	XP_011514754.1:p.Leu4369=
XM_011516453.1:c.13023C>G	XP_011514755.1:p.Leu4341=
XM_011516454.1:c.12345C>G	XP_011514756.1:p.Leu4115=
XM_011516455.1:c.10806C>G	XP_011514757.1:p.Leu3602=
XM_011516456.1:c.13212C>G	XP_011514758.1:p.Leu4404=
XM_005250025.4:c.13260C>G	XP_005250082.1:p.Leu4420=
XM_005250026.3:c.13257C>G	XP_005250083.1:p.Leu4419=
XM_005250027.4:c.13257C>G	XP_005250084.1:p.Leu4419=
XM_005250028.4:c.13260C>G	XP_005250085.1:p.Leu4420=
XM_005250031.4:c.13095C>G	XP_005250088.1:p.Leu4365=
XM_006716077.3:c.13257C>G	XP_006716140.1:p.Leu4419=
XM_006716078.3:c.13188C>G	XP_006716141.1:p.Leu4396=
XM_006716079.3:c.13092C>G	XP_006716142.1:p.Leu4364=
XM_011516450.2:c.13212C>G	XP_011514752.1:p.Leu4404=
XM_011516451.2:c.13140C>G	XP_011514753.1:p.Leu4380=
XM_011516452.2:c.13107C>G	XP_011514754.1:p.Leu4369=
XM_011516453.2:c.13023C>G	XP_011514755.1:p.Leu4341=
XM_011516454.2:c.12345C>G	XP_011514756.1:p.Leu4115=
XM_011516456.2:c.13212C>G	XP_011514758.1:p.Leu4404=
XM_017012480.1:c.13260C>G	XP_016867969.1:p.Leu4420=
XM_017012481.1:c.13257C>G	XP_016867970.1:p.Leu4419=
XM_017012482.1:c.13257C>G	XP_016867971.1:p.Leu4419=
XM_017012483.1:c.13257C>G	XP_016867972.1:p.Leu4419=
XM_017012484.1:c.13227C>G	XP_016867973.1:p.Leu4409=
XM_017012485.1:c.13209C>G	XP_016867974.1:p.Leu4403=
XM_017012486.1:c.13185C>G	XP_016867975.1:p.Leu4395=
XM_017012487.1:c.13113C>G	XP_016867976.1:p.Leu4371=
XM_017012488.1:c.13077C>G	XP_016867977.1:p.Leu4359=
XM_017012489.1:c.9930C>G	XP_016867978.1:p.Leu3310=
XM_017012490.2:c.9534C>G	XP_016867979.1:p.Leu3178=
XM_024446852.1:c.13257C>G	XP_024302620.1:p.Leu4419=
XM_024446853.1:c.13185C>G	XP_024302621.1:p.Leu4395=
NM_170606.3:c.13044C>G MANE Select	NP_733751.2:p.Leu4348=