Canonical Allele Identifier: CA370093376

Gene: KMT2C

Linked Data

• dbSNP Id: rs1403649813
• MyVariant Identifiers: chr7:g.151845965A>C (hg19) ; chr7:g.152148880A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148880A>C , CM000669.2:g.152148880A>C	GRCh38
NC_000007.13:g.151845965A>C , CM000669.1:g.151845965A>C	GRCh37
NC_000007.12:g.151476898A>C	NCBI36
NG_033948.1:g.292126T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1235T>G
ENST00000682116.1:n.2179T>G
ENST00000682283.1:c.13218T>G	ENSP00000507485.1:p.Asn4406Lys
ENST00000682629.1:n.2347T>G
ENST00000683120.1:n.8239T>G
ENST00000683178.1:c.3620T>G
ENST00000683200.1:c.10557T>G	ENSP00000508052.1:p.Asn3519Lys
ENST00000683337.1:n.4677T>G
ENST00000683502.1:c.3692T>G
ENST00000683621.1:n.1813T>G
ENST00000683640.1:n.1763T>G
ENST00000684069.1:c.1464T>G	ENSP00000507650.1:p.Asn488Lys
ENST00000684261.1:c.7944T>G	ENSP00000508097.1:p.Asn2648Lys
ENST00000684649.1:c.3692T>G
ENST00000262189.11:c.13047T>G MANE Select	ENSP00000262189.6:p.Asn4349Lys
ENST00000360104.8:c.8834T>G
ENST00000418061.2:c.3689T>G
ENST00000424877.6:c.3623T>G
ENST00000679393.1:n.7758T>G
ENST00000679560.1:c.7947T>G	ENSP00000505094.1:p.Asn2649Lys
ENST00000679882.1:c.12612T>G	ENSP00000506154.1:p.Asn4204Lys
ENST00000680029.1:c.3624T>G
ENST00000680877.1:c.7947T>G	ENSP00000505724.1:p.Asn2649Lys
ENST00000681923.1:n.2062T>G
ENST00000262189.10:c.13047T>G	ENSP00000262189.6:p.Asn4349Lys
ENST00000355193.6:c.13047T>G	ENSP00000347325.3:p.Asn4349Lys
ENST00000360104.7:c.5728T>G
ENST00000424877.5:c.2898T>G	ENSP00000410411.1:p.Asn966Lys
ENST00000473186.5:n.10929T>G
ENST00000558084.5:c.*10567T>G	ENSP00000453752.1:n.*10567T>G
NM_170606.2:c.13047T>G	NP_733751.2:p.Asn4349Lys
XM_005250025.3:c.13263T>G	XP_005250082.1:p.Asn4421Lys
XM_005250026.2:c.13260T>G	XP_005250083.1:p.Asn4420Lys
XM_005250027.3:c.13260T>G	XP_005250084.1:p.Asn4420Lys
XM_005250028.3:c.13263T>G	XP_005250085.1:p.Asn4421Lys
XM_005250031.3:c.13098T>G	XP_005250088.1:p.Asn4366Lys
XM_006716077.2:c.13260T>G	XP_006716140.1:p.Asn4420Lys
XM_006716078.2:c.13191T>G	XP_006716141.1:p.Asn4397Lys
XM_006716079.2:c.13095T>G	XP_006716142.1:p.Asn4365Lys
XM_011516450.1:c.13215T>G	XP_011514752.1:p.Asn4405Lys
XM_011516451.1:c.13143T>G	XP_011514753.1:p.Asn4381Lys
XM_011516452.1:c.13110T>G	XP_011514754.1:p.Asn4370Lys
XM_011516453.1:c.13026T>G	XP_011514755.1:p.Asn4342Lys
XM_011516454.1:c.12348T>G	XP_011514756.1:p.Asn4116Lys
XM_011516455.1:c.10809T>G	XP_011514757.1:p.Asn3603Lys
XM_011516456.1:c.13215T>G	XP_011514758.1:p.Asn4405Lys
XM_005250025.4:c.13263T>G	XP_005250082.1:p.Asn4421Lys
XM_005250026.3:c.13260T>G	XP_005250083.1:p.Asn4420Lys
XM_005250027.4:c.13260T>G	XP_005250084.1:p.Asn4420Lys
XM_005250028.4:c.13263T>G	XP_005250085.1:p.Asn4421Lys
XM_005250031.4:c.13098T>G	XP_005250088.1:p.Asn4366Lys
XM_006716077.3:c.13260T>G	XP_006716140.1:p.Asn4420Lys
XM_006716078.3:c.13191T>G	XP_006716141.1:p.Asn4397Lys
XM_006716079.3:c.13095T>G	XP_006716142.1:p.Asn4365Lys
XM_011516450.2:c.13215T>G	XP_011514752.1:p.Asn4405Lys
XM_011516451.2:c.13143T>G	XP_011514753.1:p.Asn4381Lys
XM_011516452.2:c.13110T>G	XP_011514754.1:p.Asn4370Lys
XM_011516453.2:c.13026T>G	XP_011514755.1:p.Asn4342Lys
XM_011516454.2:c.12348T>G	XP_011514756.1:p.Asn4116Lys
XM_011516456.2:c.13215T>G	XP_011514758.1:p.Asn4405Lys
XM_017012480.1:c.13263T>G	XP_016867969.1:p.Asn4421Lys
XM_017012481.1:c.13260T>G	XP_016867970.1:p.Asn4420Lys
XM_017012482.1:c.13260T>G	XP_016867971.1:p.Asn4420Lys
XM_017012483.1:c.13260T>G	XP_016867972.1:p.Asn4420Lys
XM_017012484.1:c.13230T>G	XP_016867973.1:p.Asn4410Lys
XM_017012485.1:c.13212T>G	XP_016867974.1:p.Asn4404Lys
XM_017012486.1:c.13188T>G	XP_016867975.1:p.Asn4396Lys
XM_017012487.1:c.13116T>G	XP_016867976.1:p.Asn4372Lys
XM_017012488.1:c.13080T>G	XP_016867977.1:p.Asn4360Lys
XM_017012489.1:c.9933T>G	XP_016867978.1:p.Asn3311Lys
XM_017012490.2:c.9537T>G	XP_016867979.1:p.Asn3179Lys
XM_024446852.1:c.13260T>G	XP_024302620.1:p.Asn4420Lys
XM_024446853.1:c.13188T>G	XP_024302621.1:p.Asn4396Lys
NM_170606.3:c.13047T>G MANE Select	NP_733751.2:p.Asn4349Lys