Canonical Allele Identifier: CA370093385

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845967T>A (hg19) ; chr7:g.152148882T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148882T>A , CM000669.2:g.152148882T>A	GRCh38
NC_000007.13:g.151845967T>A , CM000669.1:g.151845967T>A	GRCh37
NC_000007.12:g.151476900T>A	NCBI36
NG_033948.1:g.292124A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1233A>T
ENST00000682116.1:n.2177A>T
ENST00000682283.1:c.13216A>T	ENSP00000507485.1:p.Asn4406Tyr
ENST00000682629.1:n.2345A>T
ENST00000683120.1:n.8237A>T
ENST00000683178.1:c.3618A>T
ENST00000683200.1:c.10555A>T	ENSP00000508052.1:p.Asn3519Tyr
ENST00000683337.1:n.4675A>T
ENST00000683502.1:c.3690A>T
ENST00000683621.1:n.1811A>T
ENST00000683640.1:n.1761A>T
ENST00000684069.1:c.1462A>T	ENSP00000507650.1:p.Asn488Tyr
ENST00000684261.1:c.7942A>T	ENSP00000508097.1:p.Asn2648Tyr
ENST00000684649.1:c.3690A>T
ENST00000262189.11:c.13045A>T MANE Select	ENSP00000262189.6:p.Asn4349Tyr
ENST00000360104.8:c.8832A>T
ENST00000418061.2:c.3687A>T
ENST00000424877.6:c.3621A>T
ENST00000679393.1:n.7756A>T
ENST00000679560.1:c.7945A>T	ENSP00000505094.1:p.Asn2649Tyr
ENST00000679882.1:c.12610A>T	ENSP00000506154.1:p.Asn4204Tyr
ENST00000680029.1:c.3622A>T
ENST00000680877.1:c.7945A>T	ENSP00000505724.1:p.Asn2649Tyr
ENST00000681923.1:n.2060A>T
ENST00000262189.10:c.13045A>T	ENSP00000262189.6:p.Asn4349Tyr
ENST00000355193.6:c.13045A>T	ENSP00000347325.3:p.Asn4349Tyr
ENST00000360104.7:c.5726A>T
ENST00000424877.5:c.2896A>T	ENSP00000410411.1:p.Asn966Tyr
ENST00000473186.5:n.10927A>T
ENST00000558084.5:c.*10565A>T	ENSP00000453752.1:n.*10565A>T
NM_170606.2:c.13045A>T	NP_733751.2:p.Asn4349Tyr
XM_005250025.3:c.13261A>T	XP_005250082.1:p.Asn4421Tyr
XM_005250026.2:c.13258A>T	XP_005250083.1:p.Asn4420Tyr
XM_005250027.3:c.13258A>T	XP_005250084.1:p.Asn4420Tyr
XM_005250028.3:c.13261A>T	XP_005250085.1:p.Asn4421Tyr
XM_005250031.3:c.13096A>T	XP_005250088.1:p.Asn4366Tyr
XM_006716077.2:c.13258A>T	XP_006716140.1:p.Asn4420Tyr
XM_006716078.2:c.13189A>T	XP_006716141.1:p.Asn4397Tyr
XM_006716079.2:c.13093A>T	XP_006716142.1:p.Asn4365Tyr
XM_011516450.1:c.13213A>T	XP_011514752.1:p.Asn4405Tyr
XM_011516451.1:c.13141A>T	XP_011514753.1:p.Asn4381Tyr
XM_011516452.1:c.13108A>T	XP_011514754.1:p.Asn4370Tyr
XM_011516453.1:c.13024A>T	XP_011514755.1:p.Asn4342Tyr
XM_011516454.1:c.12346A>T	XP_011514756.1:p.Asn4116Tyr
XM_011516455.1:c.10807A>T	XP_011514757.1:p.Asn3603Tyr
XM_011516456.1:c.13213A>T	XP_011514758.1:p.Asn4405Tyr
XM_005250025.4:c.13261A>T	XP_005250082.1:p.Asn4421Tyr
XM_005250026.3:c.13258A>T	XP_005250083.1:p.Asn4420Tyr
XM_005250027.4:c.13258A>T	XP_005250084.1:p.Asn4420Tyr
XM_005250028.4:c.13261A>T	XP_005250085.1:p.Asn4421Tyr
XM_005250031.4:c.13096A>T	XP_005250088.1:p.Asn4366Tyr
XM_006716077.3:c.13258A>T	XP_006716140.1:p.Asn4420Tyr
XM_006716078.3:c.13189A>T	XP_006716141.1:p.Asn4397Tyr
XM_006716079.3:c.13093A>T	XP_006716142.1:p.Asn4365Tyr
XM_011516450.2:c.13213A>T	XP_011514752.1:p.Asn4405Tyr
XM_011516451.2:c.13141A>T	XP_011514753.1:p.Asn4381Tyr
XM_011516452.2:c.13108A>T	XP_011514754.1:p.Asn4370Tyr
XM_011516453.2:c.13024A>T	XP_011514755.1:p.Asn4342Tyr
XM_011516454.2:c.12346A>T	XP_011514756.1:p.Asn4116Tyr
XM_011516456.2:c.13213A>T	XP_011514758.1:p.Asn4405Tyr
XM_017012480.1:c.13261A>T	XP_016867969.1:p.Asn4421Tyr
XM_017012481.1:c.13258A>T	XP_016867970.1:p.Asn4420Tyr
XM_017012482.1:c.13258A>T	XP_016867971.1:p.Asn4420Tyr
XM_017012483.1:c.13258A>T	XP_016867972.1:p.Asn4420Tyr
XM_017012484.1:c.13228A>T	XP_016867973.1:p.Asn4410Tyr
XM_017012485.1:c.13210A>T	XP_016867974.1:p.Asn4404Tyr
XM_017012486.1:c.13186A>T	XP_016867975.1:p.Asn4396Tyr
XM_017012487.1:c.13114A>T	XP_016867976.1:p.Asn4372Tyr
XM_017012488.1:c.13078A>T	XP_016867977.1:p.Asn4360Tyr
XM_017012489.1:c.9931A>T	XP_016867978.1:p.Asn3311Tyr
XM_017012490.2:c.9535A>T	XP_016867979.1:p.Asn3179Tyr
XM_024446852.1:c.13258A>T	XP_024302620.1:p.Asn4420Tyr
XM_024446853.1:c.13186A>T	XP_024302621.1:p.Asn4396Tyr
NM_170606.3:c.13045A>T MANE Select	NP_733751.2:p.Asn4349Tyr