Canonical Allele Identifier: CA370093381

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845966T>G (hg19) ; chr7:g.152148881T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148881T>G , CM000669.2:g.152148881T>G	GRCh38
NC_000007.13:g.151845966T>G , CM000669.1:g.151845966T>G	GRCh37
NC_000007.12:g.151476899T>G	NCBI36
NG_033948.1:g.292125A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1234A>C
ENST00000682116.1:n.2178A>C
ENST00000682283.1:c.13217A>C	ENSP00000507485.1:p.Asn4406Thr
ENST00000682629.1:n.2346A>C
ENST00000683120.1:n.8238A>C
ENST00000683178.1:c.3619A>C
ENST00000683200.1:c.10556A>C	ENSP00000508052.1:p.Asn3519Thr
ENST00000683337.1:n.4676A>C
ENST00000683502.1:c.3691A>C
ENST00000683621.1:n.1812A>C
ENST00000683640.1:n.1762A>C
ENST00000684069.1:c.1463A>C	ENSP00000507650.1:p.Asn488Thr
ENST00000684261.1:c.7943A>C	ENSP00000508097.1:p.Asn2648Thr
ENST00000684649.1:c.3691A>C
ENST00000262189.11:c.13046A>C MANE Select	ENSP00000262189.6:p.Asn4349Thr
ENST00000360104.8:c.8833A>C
ENST00000418061.2:c.3688A>C
ENST00000424877.6:c.3622A>C
ENST00000679393.1:n.7757A>C
ENST00000679560.1:c.7946A>C	ENSP00000505094.1:p.Asn2649Thr
ENST00000679882.1:c.12611A>C	ENSP00000506154.1:p.Asn4204Thr
ENST00000680029.1:c.3623A>C
ENST00000680877.1:c.7946A>C	ENSP00000505724.1:p.Asn2649Thr
ENST00000681923.1:n.2061A>C
ENST00000262189.10:c.13046A>C	ENSP00000262189.6:p.Asn4349Thr
ENST00000355193.6:c.13046A>C	ENSP00000347325.3:p.Asn4349Thr
ENST00000360104.7:c.5727A>C
ENST00000424877.5:c.2897A>C	ENSP00000410411.1:p.Asn966Thr
ENST00000473186.5:n.10928A>C
ENST00000558084.5:c.*10566A>C	ENSP00000453752.1:n.*10566A>C
NM_170606.2:c.13046A>C	NP_733751.2:p.Asn4349Thr
XM_005250025.3:c.13262A>C	XP_005250082.1:p.Asn4421Thr
XM_005250026.2:c.13259A>C	XP_005250083.1:p.Asn4420Thr
XM_005250027.3:c.13259A>C	XP_005250084.1:p.Asn4420Thr
XM_005250028.3:c.13262A>C	XP_005250085.1:p.Asn4421Thr
XM_005250031.3:c.13097A>C	XP_005250088.1:p.Asn4366Thr
XM_006716077.2:c.13259A>C	XP_006716140.1:p.Asn4420Thr
XM_006716078.2:c.13190A>C	XP_006716141.1:p.Asn4397Thr
XM_006716079.2:c.13094A>C	XP_006716142.1:p.Asn4365Thr
XM_011516450.1:c.13214A>C	XP_011514752.1:p.Asn4405Thr
XM_011516451.1:c.13142A>C	XP_011514753.1:p.Asn4381Thr
XM_011516452.1:c.13109A>C	XP_011514754.1:p.Asn4370Thr
XM_011516453.1:c.13025A>C	XP_011514755.1:p.Asn4342Thr
XM_011516454.1:c.12347A>C	XP_011514756.1:p.Asn4116Thr
XM_011516455.1:c.10808A>C	XP_011514757.1:p.Asn3603Thr
XM_011516456.1:c.13214A>C	XP_011514758.1:p.Asn4405Thr
XM_005250025.4:c.13262A>C	XP_005250082.1:p.Asn4421Thr
XM_005250026.3:c.13259A>C	XP_005250083.1:p.Asn4420Thr
XM_005250027.4:c.13259A>C	XP_005250084.1:p.Asn4420Thr
XM_005250028.4:c.13262A>C	XP_005250085.1:p.Asn4421Thr
XM_005250031.4:c.13097A>C	XP_005250088.1:p.Asn4366Thr
XM_006716077.3:c.13259A>C	XP_006716140.1:p.Asn4420Thr
XM_006716078.3:c.13190A>C	XP_006716141.1:p.Asn4397Thr
XM_006716079.3:c.13094A>C	XP_006716142.1:p.Asn4365Thr
XM_011516450.2:c.13214A>C	XP_011514752.1:p.Asn4405Thr
XM_011516451.2:c.13142A>C	XP_011514753.1:p.Asn4381Thr
XM_011516452.2:c.13109A>C	XP_011514754.1:p.Asn4370Thr
XM_011516453.2:c.13025A>C	XP_011514755.1:p.Asn4342Thr
XM_011516454.2:c.12347A>C	XP_011514756.1:p.Asn4116Thr
XM_011516456.2:c.13214A>C	XP_011514758.1:p.Asn4405Thr
XM_017012480.1:c.13262A>C	XP_016867969.1:p.Asn4421Thr
XM_017012481.1:c.13259A>C	XP_016867970.1:p.Asn4420Thr
XM_017012482.1:c.13259A>C	XP_016867971.1:p.Asn4420Thr
XM_017012483.1:c.13259A>C	XP_016867972.1:p.Asn4420Thr
XM_017012484.1:c.13229A>C	XP_016867973.1:p.Asn4410Thr
XM_017012485.1:c.13211A>C	XP_016867974.1:p.Asn4404Thr
XM_017012486.1:c.13187A>C	XP_016867975.1:p.Asn4396Thr
XM_017012487.1:c.13115A>C	XP_016867976.1:p.Asn4372Thr
XM_017012488.1:c.13079A>C	XP_016867977.1:p.Asn4360Thr
XM_017012489.1:c.9932A>C	XP_016867978.1:p.Asn3311Thr
XM_017012490.2:c.9536A>C	XP_016867979.1:p.Asn3179Thr
XM_024446852.1:c.13259A>C	XP_024302620.1:p.Asn4420Thr
XM_024446853.1:c.13187A>C	XP_024302621.1:p.Asn4396Thr
NM_170606.3:c.13046A>C MANE Select	NP_733751.2:p.Asn4349Thr