Canonical Allele Identifier: CA370093363

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845961T>A (hg19) ; chr7:g.152148876T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148876T>A , CM000669.2:g.152148876T>A	GRCh38
NC_000007.13:g.151845961T>A , CM000669.1:g.151845961T>A	GRCh37
NC_000007.12:g.151476894T>A	NCBI36
NG_033948.1:g.292130A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1239A>T
ENST00000682116.1:n.2183A>T
ENST00000682283.1:c.13222A>T	ENSP00000507485.1:p.Lys4408Ter
ENST00000682629.1:n.2351A>T
ENST00000683120.1:n.8243A>T
ENST00000683178.1:c.3624A>T
ENST00000683200.1:c.10561A>T	ENSP00000508052.1:p.Lys3521Ter
ENST00000683337.1:n.4681A>T
ENST00000683502.1:c.3696A>T
ENST00000683621.1:n.1817A>T
ENST00000683640.1:n.1767A>T
ENST00000684069.1:c.1468A>T	ENSP00000507650.1:p.Lys490Ter
ENST00000684261.1:c.7948A>T	ENSP00000508097.1:p.Lys2650Ter
ENST00000684649.1:c.3696A>T
ENST00000262189.11:c.13051A>T MANE Select	ENSP00000262189.6:p.Lys4351Ter
ENST00000360104.8:c.8838A>T
ENST00000418061.2:c.3693A>T
ENST00000424877.6:c.3627A>T
ENST00000679393.1:n.7762A>T
ENST00000679560.1:c.7951A>T	ENSP00000505094.1:p.Lys2651Ter
ENST00000679882.1:c.12616A>T	ENSP00000506154.1:p.Lys4206Ter
ENST00000680029.1:c.3628A>T
ENST00000680877.1:c.7951A>T	ENSP00000505724.1:p.Lys2651Ter
ENST00000681923.1:n.2066A>T
ENST00000262189.10:c.13051A>T	ENSP00000262189.6:p.Lys4351Ter
ENST00000355193.6:c.13051A>T	ENSP00000347325.3:p.Lys4351Ter
ENST00000360104.7:c.5732A>T
ENST00000424877.5:c.2902A>T	ENSP00000410411.1:p.Lys968Ter
ENST00000473186.5:n.10933A>T
ENST00000558084.5:c.*10571A>T	ENSP00000453752.1:n.*10571A>T
NM_170606.2:c.13051A>T	NP_733751.2:p.Lys4351Ter
XM_005250025.3:c.13267A>T	XP_005250082.1:p.Lys4423Ter
XM_005250026.2:c.13264A>T	XP_005250083.1:p.Lys4422Ter
XM_005250027.3:c.13264A>T	XP_005250084.1:p.Lys4422Ter
XM_005250028.3:c.13267A>T	XP_005250085.1:p.Lys4423Ter
XM_005250031.3:c.13102A>T	XP_005250088.1:p.Lys4368Ter
XM_006716077.2:c.13264A>T	XP_006716140.1:p.Lys4422Ter
XM_006716078.2:c.13195A>T	XP_006716141.1:p.Lys4399Ter
XM_006716079.2:c.13099A>T	XP_006716142.1:p.Lys4367Ter
XM_011516450.1:c.13219A>T	XP_011514752.1:p.Lys4407Ter
XM_011516451.1:c.13147A>T	XP_011514753.1:p.Lys4383Ter
XM_011516452.1:c.13114A>T	XP_011514754.1:p.Lys4372Ter
XM_011516453.1:c.13030A>T	XP_011514755.1:p.Lys4344Ter
XM_011516454.1:c.12352A>T	XP_011514756.1:p.Lys4118Ter
XM_011516455.1:c.10813A>T	XP_011514757.1:p.Lys3605Ter
XM_011516456.1:c.13219A>T	XP_011514758.1:p.Lys4407Ter
XM_005250025.4:c.13267A>T	XP_005250082.1:p.Lys4423Ter
XM_005250026.3:c.13264A>T	XP_005250083.1:p.Lys4422Ter
XM_005250027.4:c.13264A>T	XP_005250084.1:p.Lys4422Ter
XM_005250028.4:c.13267A>T	XP_005250085.1:p.Lys4423Ter
XM_005250031.4:c.13102A>T	XP_005250088.1:p.Lys4368Ter
XM_006716077.3:c.13264A>T	XP_006716140.1:p.Lys4422Ter
XM_006716078.3:c.13195A>T	XP_006716141.1:p.Lys4399Ter
XM_006716079.3:c.13099A>T	XP_006716142.1:p.Lys4367Ter
XM_011516450.2:c.13219A>T	XP_011514752.1:p.Lys4407Ter
XM_011516451.2:c.13147A>T	XP_011514753.1:p.Lys4383Ter
XM_011516452.2:c.13114A>T	XP_011514754.1:p.Lys4372Ter
XM_011516453.2:c.13030A>T	XP_011514755.1:p.Lys4344Ter
XM_011516454.2:c.12352A>T	XP_011514756.1:p.Lys4118Ter
XM_011516456.2:c.13219A>T	XP_011514758.1:p.Lys4407Ter
XM_017012480.1:c.13267A>T	XP_016867969.1:p.Lys4423Ter
XM_017012481.1:c.13264A>T	XP_016867970.1:p.Lys4422Ter
XM_017012482.1:c.13264A>T	XP_016867971.1:p.Lys4422Ter
XM_017012483.1:c.13264A>T	XP_016867972.1:p.Lys4422Ter
XM_017012484.1:c.13234A>T	XP_016867973.1:p.Lys4412Ter
XM_017012485.1:c.13216A>T	XP_016867974.1:p.Lys4406Ter
XM_017012486.1:c.13192A>T	XP_016867975.1:p.Lys4398Ter
XM_017012487.1:c.13120A>T	XP_016867976.1:p.Lys4374Ter
XM_017012488.1:c.13084A>T	XP_016867977.1:p.Lys4362Ter
XM_017012489.1:c.9937A>T	XP_016867978.1:p.Lys3313Ter
XM_017012490.2:c.9541A>T	XP_016867979.1:p.Lys3181Ter
XM_024446852.1:c.13264A>T	XP_024302620.1:p.Lys4422Ter
XM_024446853.1:c.13192A>T	XP_024302621.1:p.Lys4398Ter
NM_170606.3:c.13051A>T MANE Select	NP_733751.2:p.Lys4351Ter