Canonical Allele Identifier: CA370093322

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845951C>A (hg19) ; chr7:g.152148866C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148866C>A , CM000669.2:g.152148866C>A	GRCh38
NC_000007.13:g.151845951C>A , CM000669.1:g.151845951C>A	GRCh37
NC_000007.12:g.151476884C>A	NCBI36
NG_033948.1:g.292140G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1249G>T
ENST00000682116.1:n.2193G>T
ENST00000682283.1:c.13232G>T	ENSP00000507485.1:p.Gly4411Val
ENST00000682629.1:n.2361G>T
ENST00000683120.1:n.8253G>T
ENST00000683178.1:c.3634G>T
ENST00000683200.1:c.10571G>T	ENSP00000508052.1:p.Gly3524Val
ENST00000683337.1:n.4691G>T
ENST00000683502.1:c.3706G>T
ENST00000683621.1:n.1827G>T
ENST00000683640.1:n.1777G>T
ENST00000684069.1:c.1478G>T	ENSP00000507650.1:p.Gly493Val
ENST00000684261.1:c.7958G>T	ENSP00000508097.1:p.Gly2653Val
ENST00000684649.1:c.3706G>T
ENST00000262189.11:c.13061G>T MANE Select	ENSP00000262189.6:p.Gly4354Val
ENST00000360104.8:c.8848G>T
ENST00000418061.2:c.3703G>T
ENST00000424877.6:c.3637G>T
ENST00000679393.1:n.7772G>T
ENST00000679560.1:c.7961G>T	ENSP00000505094.1:p.Gly2654Val
ENST00000679882.1:c.12626G>T	ENSP00000506154.1:p.Gly4209Val
ENST00000680029.1:c.3638G>T
ENST00000680877.1:c.7961G>T	ENSP00000505724.1:p.Gly2654Val
ENST00000681923.1:n.2076G>T
ENST00000262189.10:c.13061G>T	ENSP00000262189.6:p.Gly4354Val
ENST00000355193.6:c.13061G>T	ENSP00000347325.3:p.Gly4354Val
ENST00000360104.7:c.5742G>T
ENST00000424877.5:c.2912G>T	ENSP00000410411.1:p.Gly971Val
ENST00000473186.5:n.10943G>T
ENST00000558084.5:c.*10581G>T	ENSP00000453752.1:n.*10581G>T
NM_170606.2:c.13061G>T	NP_733751.2:p.Gly4354Val
XM_005250025.3:c.13277G>T	XP_005250082.1:p.Gly4426Val
XM_005250026.2:c.13274G>T	XP_005250083.1:p.Gly4425Val
XM_005250027.3:c.13274G>T	XP_005250084.1:p.Gly4425Val
XM_005250028.3:c.13277G>T	XP_005250085.1:p.Gly4426Val
XM_005250031.3:c.13112G>T	XP_005250088.1:p.Gly4371Val
XM_006716077.2:c.13274G>T	XP_006716140.1:p.Gly4425Val
XM_006716078.2:c.13205G>T	XP_006716141.1:p.Gly4402Val
XM_006716079.2:c.13109G>T	XP_006716142.1:p.Gly4370Val
XM_011516450.1:c.13229G>T	XP_011514752.1:p.Gly4410Val
XM_011516451.1:c.13157G>T	XP_011514753.1:p.Gly4386Val
XM_011516452.1:c.13124G>T	XP_011514754.1:p.Gly4375Val
XM_011516453.1:c.13040G>T	XP_011514755.1:p.Gly4347Val
XM_011516454.1:c.12362G>T	XP_011514756.1:p.Gly4121Val
XM_011516455.1:c.10823G>T	XP_011514757.1:p.Gly3608Val
XM_011516456.1:c.13229G>T	XP_011514758.1:p.Gly4410Val
XM_005250025.4:c.13277G>T	XP_005250082.1:p.Gly4426Val
XM_005250026.3:c.13274G>T	XP_005250083.1:p.Gly4425Val
XM_005250027.4:c.13274G>T	XP_005250084.1:p.Gly4425Val
XM_005250028.4:c.13277G>T	XP_005250085.1:p.Gly4426Val
XM_005250031.4:c.13112G>T	XP_005250088.1:p.Gly4371Val
XM_006716077.3:c.13274G>T	XP_006716140.1:p.Gly4425Val
XM_006716078.3:c.13205G>T	XP_006716141.1:p.Gly4402Val
XM_006716079.3:c.13109G>T	XP_006716142.1:p.Gly4370Val
XM_011516450.2:c.13229G>T	XP_011514752.1:p.Gly4410Val
XM_011516451.2:c.13157G>T	XP_011514753.1:p.Gly4386Val
XM_011516452.2:c.13124G>T	XP_011514754.1:p.Gly4375Val
XM_011516453.2:c.13040G>T	XP_011514755.1:p.Gly4347Val
XM_011516454.2:c.12362G>T	XP_011514756.1:p.Gly4121Val
XM_011516456.2:c.13229G>T	XP_011514758.1:p.Gly4410Val
XM_017012480.1:c.13277G>T	XP_016867969.1:p.Gly4426Val
XM_017012481.1:c.13274G>T	XP_016867970.1:p.Gly4425Val
XM_017012482.1:c.13274G>T	XP_016867971.1:p.Gly4425Val
XM_017012483.1:c.13274G>T	XP_016867972.1:p.Gly4425Val
XM_017012484.1:c.13244G>T	XP_016867973.1:p.Gly4415Val
XM_017012485.1:c.13226G>T	XP_016867974.1:p.Gly4409Val
XM_017012486.1:c.13202G>T	XP_016867975.1:p.Gly4401Val
XM_017012487.1:c.13130G>T	XP_016867976.1:p.Gly4377Val
XM_017012488.1:c.13094G>T	XP_016867977.1:p.Gly4365Val
XM_017012489.1:c.9947G>T	XP_016867978.1:p.Gly3316Val
XM_017012490.2:c.9551G>T	XP_016867979.1:p.Gly3184Val
XM_024446852.1:c.13274G>T	XP_024302620.1:p.Gly4425Val
XM_024446853.1:c.13202G>T	XP_024302621.1:p.Gly4401Val
NM_170606.3:c.13061G>T MANE Select	NP_733751.2:p.Gly4354Val