Canonical Allele Identifier: CA458884951

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845965_151845966insT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148882dup , CM000669.2:g.152148882dup	GRCh38
NC_000007.13:g.151845967dup , CM000669.1:g.151845967dup	GRCh37
NC_000007.12:g.151476900dup	NCBI36
NG_033948.1:g.292125dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1234dup
ENST00000682116.1:n.2178dup
ENST00000682283.1:c.13217dup	ENSP00000507485.1:p.Asn4406LysfsTer2
ENST00000682629.1:n.2346dup
ENST00000683120.1:n.8238dup
ENST00000683178.1:c.3619dup
ENST00000683200.1:c.10556dup	ENSP00000508052.1:p.Asn3519LysfsTer2
ENST00000683337.1:n.4676dup
ENST00000683502.1:c.3691dup
ENST00000683621.1:n.1812dup
ENST00000683640.1:n.1762dup
ENST00000684069.1:c.1463dup	ENSP00000507650.1:p.Asn488LysfsTer2
ENST00000684261.1:c.7943dup	ENSP00000508097.1:p.Asn2648LysfsTer2
ENST00000684649.1:c.3691dup
ENST00000262189.11:c.13046dup MANE Select	ENSP00000262189.6:p.Asn4349LysfsTer2
ENST00000360104.8:c.8833dup
ENST00000418061.2:c.3688dup
ENST00000424877.6:c.3622dup
ENST00000679393.1:n.7757dup
ENST00000679560.1:c.7946dup	ENSP00000505094.1:p.Asn2649LysfsTer2
ENST00000679882.1:c.12611dup	ENSP00000506154.1:p.Asn4204LysfsTer2
ENST00000680029.1:c.3623dup
ENST00000680877.1:c.7946dup	ENSP00000505724.1:p.Asn2649LysfsTer2
ENST00000681923.1:n.2061dup
ENST00000262189.10:c.13046dup	ENSP00000262189.6:p.Asn4349LysfsTer2
ENST00000355193.6:c.13046dup	ENSP00000347325.3:p.Asn4349LysfsTer2
ENST00000360104.7:c.5727dup
ENST00000424877.5:c.2897dup	ENSP00000410411.1:p.Asn966LysfsTer2
ENST00000473186.5:n.10928dup
ENST00000558084.5:c.*10566dup	ENSP00000453752.1:n.*10566dup
NM_170606.2:c.13046dup	NP_733751.2:p.Asn4349LysfsTer2
XM_005250025.3:c.13262dup	XP_005250082.1:p.Asn4421LysfsTer2
XM_005250026.2:c.13259dup	XP_005250083.1:p.Asn4420LysfsTer2
XM_005250027.3:c.13259dup	XP_005250084.1:p.Asn4420LysfsTer2
XM_005250028.3:c.13262dup	XP_005250085.1:p.Asn4421LysfsTer2
XM_005250031.3:c.13097dup	XP_005250088.1:p.Asn4366LysfsTer2
XM_006716077.2:c.13259dup	XP_006716140.1:p.Asn4420LysfsTer2
XM_006716078.2:c.13190dup	XP_006716141.1:p.Asn4397LysfsTer2
XM_006716079.2:c.13094dup	XP_006716142.1:p.Asn4365LysfsTer2
XM_011516450.1:c.13214dup	XP_011514752.1:p.Asn4405LysfsTer2
XM_011516451.1:c.13142dup	XP_011514753.1:p.Asn4381LysfsTer2
XM_011516452.1:c.13109dup	XP_011514754.1:p.Asn4370LysfsTer2
XM_011516453.1:c.13025dup	XP_011514755.1:p.Asn4342LysfsTer2
XM_011516454.1:c.12347dup	XP_011514756.1:p.Asn4116LysfsTer2
XM_011516455.1:c.10808dup	XP_011514757.1:p.Asn3603LysfsTer2
XM_011516456.1:c.13214dup	XP_011514758.1:p.Asn4405LysfsTer2
XM_005250025.4:c.13262dup	XP_005250082.1:p.Asn4421LysfsTer2
XM_005250026.3:c.13259dup	XP_005250083.1:p.Asn4420LysfsTer2
XM_005250027.4:c.13259dup	XP_005250084.1:p.Asn4420LysfsTer2
XM_005250028.4:c.13262dup	XP_005250085.1:p.Asn4421LysfsTer2
XM_005250031.4:c.13097dup	XP_005250088.1:p.Asn4366LysfsTer2
XM_006716077.3:c.13259dup	XP_006716140.1:p.Asn4420LysfsTer2
XM_006716078.3:c.13190dup	XP_006716141.1:p.Asn4397LysfsTer2
XM_006716079.3:c.13094dup	XP_006716142.1:p.Asn4365LysfsTer2
XM_011516450.2:c.13214dup	XP_011514752.1:p.Asn4405LysfsTer2
XM_011516451.2:c.13142dup	XP_011514753.1:p.Asn4381LysfsTer2
XM_011516452.2:c.13109dup	XP_011514754.1:p.Asn4370LysfsTer2
XM_011516453.2:c.13025dup	XP_011514755.1:p.Asn4342LysfsTer2
XM_011516454.2:c.12347dup	XP_011514756.1:p.Asn4116LysfsTer2
XM_011516456.2:c.13214dup	XP_011514758.1:p.Asn4405LysfsTer2
XM_017012480.1:c.13262dup	XP_016867969.1:p.Asn4421LysfsTer2
XM_017012481.1:c.13259dup	XP_016867970.1:p.Asn4420LysfsTer2
XM_017012482.1:c.13259dup	XP_016867971.1:p.Asn4420LysfsTer2
XM_017012483.1:c.13259dup	XP_016867972.1:p.Asn4420LysfsTer2
XM_017012484.1:c.13229dup	XP_016867973.1:p.Asn4410LysfsTer2
XM_017012485.1:c.13211dup	XP_016867974.1:p.Asn4404LysfsTer2
XM_017012486.1:c.13187dup	XP_016867975.1:p.Asn4396LysfsTer2
XM_017012487.1:c.13115dup	XP_016867976.1:p.Asn4372LysfsTer2
XM_017012488.1:c.13079dup	XP_016867977.1:p.Asn4360LysfsTer2
XM_017012489.1:c.9932dup	XP_016867978.1:p.Asn3311LysfsTer2
XM_017012490.2:c.9536dup	XP_016867979.1:p.Asn3179LysfsTer2
XM_024446852.1:c.13259dup	XP_024302620.1:p.Asn4420LysfsTer2
XM_024446853.1:c.13187dup	XP_024302621.1:p.Asn4396LysfsTer2
NM_170606.3:c.13046dup MANE Select	NP_733751.2:p.Asn4349LysfsTer2