Canonical Allele Identifier: CA370093271

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845937T>A (hg19) ; chr7:g.152148852T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148852T>A , CM000669.2:g.152148852T>A	GRCh38
NC_000007.13:g.151845937T>A , CM000669.1:g.151845937T>A	GRCh37
NC_000007.12:g.151476870T>A	NCBI36
NG_033948.1:g.292154A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1263A>T
ENST00000682116.1:n.2207A>T
ENST00000682283.1:c.13246A>T	ENSP00000507485.1:p.Lys4416Ter
ENST00000682629.1:n.2375A>T
ENST00000683120.1:n.8267A>T
ENST00000683178.1:c.3648A>T
ENST00000683200.1:c.10585A>T	ENSP00000508052.1:p.Lys3529Ter
ENST00000683337.1:n.4705A>T
ENST00000683502.1:c.3720A>T
ENST00000683621.1:n.1841A>T
ENST00000683640.1:n.1791A>T
ENST00000684069.1:c.1492A>T	ENSP00000507650.1:p.Lys498Ter
ENST00000684261.1:c.7972A>T	ENSP00000508097.1:p.Lys2658Ter
ENST00000684649.1:c.3720A>T
ENST00000262189.11:c.13075A>T MANE Select	ENSP00000262189.6:p.Lys4359Ter
ENST00000360104.8:c.8862A>T
ENST00000418061.2:c.3717A>T
ENST00000424877.6:c.3651A>T
ENST00000679393.1:n.7786A>T
ENST00000679560.1:c.7975A>T	ENSP00000505094.1:p.Lys2659Ter
ENST00000679882.1:c.12640A>T	ENSP00000506154.1:p.Lys4214Ter
ENST00000680029.1:c.3652A>T
ENST00000680877.1:c.7975A>T	ENSP00000505724.1:p.Lys2659Ter
ENST00000681923.1:n.2090A>T
ENST00000262189.10:c.13075A>T	ENSP00000262189.6:p.Lys4359Ter
ENST00000355193.6:c.13075A>T	ENSP00000347325.3:p.Lys4359Ter
ENST00000360104.7:c.5756A>T
ENST00000424877.5:c.2926A>T	ENSP00000410411.1:p.Lys976Ter
ENST00000473186.5:n.10957A>T
ENST00000558084.5:c.*10595A>T	ENSP00000453752.1:n.*10595A>T
NM_170606.2:c.13075A>T	NP_733751.2:p.Lys4359Ter
XM_005250025.3:c.13291A>T	XP_005250082.1:p.Lys4431Ter
XM_005250026.2:c.13288A>T	XP_005250083.1:p.Lys4430Ter
XM_005250027.3:c.13288A>T	XP_005250084.1:p.Lys4430Ter
XM_005250028.3:c.13291A>T	XP_005250085.1:p.Lys4431Ter
XM_005250031.3:c.13126A>T	XP_005250088.1:p.Lys4376Ter
XM_006716077.2:c.13288A>T	XP_006716140.1:p.Lys4430Ter
XM_006716078.2:c.13219A>T	XP_006716141.1:p.Lys4407Ter
XM_006716079.2:c.13123A>T	XP_006716142.1:p.Lys4375Ter
XM_011516450.1:c.13243A>T	XP_011514752.1:p.Lys4415Ter
XM_011516451.1:c.13171A>T	XP_011514753.1:p.Lys4391Ter
XM_011516452.1:c.13138A>T	XP_011514754.1:p.Lys4380Ter
XM_011516453.1:c.13054A>T	XP_011514755.1:p.Lys4352Ter
XM_011516454.1:c.12376A>T	XP_011514756.1:p.Lys4126Ter
XM_011516455.1:c.10837A>T	XP_011514757.1:p.Lys3613Ter
XM_011516456.1:c.13243A>T	XP_011514758.1:p.Lys4415Ter
XM_005250025.4:c.13291A>T	XP_005250082.1:p.Lys4431Ter
XM_005250026.3:c.13288A>T	XP_005250083.1:p.Lys4430Ter
XM_005250027.4:c.13288A>T	XP_005250084.1:p.Lys4430Ter
XM_005250028.4:c.13291A>T	XP_005250085.1:p.Lys4431Ter
XM_005250031.4:c.13126A>T	XP_005250088.1:p.Lys4376Ter
XM_006716077.3:c.13288A>T	XP_006716140.1:p.Lys4430Ter
XM_006716078.3:c.13219A>T	XP_006716141.1:p.Lys4407Ter
XM_006716079.3:c.13123A>T	XP_006716142.1:p.Lys4375Ter
XM_011516450.2:c.13243A>T	XP_011514752.1:p.Lys4415Ter
XM_011516451.2:c.13171A>T	XP_011514753.1:p.Lys4391Ter
XM_011516452.2:c.13138A>T	XP_011514754.1:p.Lys4380Ter
XM_011516453.2:c.13054A>T	XP_011514755.1:p.Lys4352Ter
XM_011516454.2:c.12376A>T	XP_011514756.1:p.Lys4126Ter
XM_011516456.2:c.13243A>T	XP_011514758.1:p.Lys4415Ter
XM_017012480.1:c.13291A>T	XP_016867969.1:p.Lys4431Ter
XM_017012481.1:c.13288A>T	XP_016867970.1:p.Lys4430Ter
XM_017012482.1:c.13288A>T	XP_016867971.1:p.Lys4430Ter
XM_017012483.1:c.13288A>T	XP_016867972.1:p.Lys4430Ter
XM_017012484.1:c.13258A>T	XP_016867973.1:p.Lys4420Ter
XM_017012485.1:c.13240A>T	XP_016867974.1:p.Lys4414Ter
XM_017012486.1:c.13216A>T	XP_016867975.1:p.Lys4406Ter
XM_017012487.1:c.13144A>T	XP_016867976.1:p.Lys4382Ter
XM_017012488.1:c.13108A>T	XP_016867977.1:p.Lys4370Ter
XM_017012489.1:c.9961A>T	XP_016867978.1:p.Lys3321Ter
XM_017012490.2:c.9565A>T	XP_016867979.1:p.Lys3189Ter
XM_024446852.1:c.13288A>T	XP_024302620.1:p.Lys4430Ter
XM_024446853.1:c.13216A>T	XP_024302621.1:p.Lys4406Ter
NM_170606.3:c.13075A>T MANE Select	NP_733751.2:p.Lys4359Ter