Canonical Allele Identifier: CA370093163

Gene: KMT2C

Linked Data

• dbSNP Id: rs2129095553
• MyVariant Identifiers: chr7:g.151845906C>A (hg19) ; chr7:g.152148821C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148821C>A , CM000669.2:g.152148821C>A	GRCh38
NC_000007.13:g.151845906C>A , CM000669.1:g.151845906C>A	GRCh37
NC_000007.12:g.151476839C>A	NCBI36
NG_033948.1:g.292185G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1294G>T
ENST00000682116.1:n.2238G>T
ENST00000682283.1:c.13277G>T	ENSP00000507485.1:p.Gly4426Val
ENST00000682629.1:n.2406G>T
ENST00000683120.1:n.8298G>T
ENST00000683178.1:c.3679G>T
ENST00000683200.1:c.10616G>T	ENSP00000508052.1:p.Gly3539Val
ENST00000683337.1:n.4736G>T
ENST00000683502.1:c.3751G>T
ENST00000683621.1:n.1872G>T
ENST00000683640.1:n.1822G>T
ENST00000684069.1:c.1523G>T	ENSP00000507650.1:p.Gly508Val
ENST00000684261.1:c.8003G>T	ENSP00000508097.1:p.Gly2668Val
ENST00000684649.1:c.3751G>T
ENST00000262189.11:c.13106G>T MANE Select	ENSP00000262189.6:p.Gly4369Val
ENST00000360104.8:c.8893G>T
ENST00000418061.2:c.3748G>T
ENST00000424877.6:c.3682G>T
ENST00000679393.1:n.7817G>T
ENST00000679560.1:c.8006G>T	ENSP00000505094.1:p.Gly2669Val
ENST00000679882.1:c.12671G>T	ENSP00000506154.1:p.Gly4224Val
ENST00000680029.1:c.3683G>T
ENST00000680877.1:c.8006G>T	ENSP00000505724.1:p.Gly2669Val
ENST00000681923.1:n.2121G>T
ENST00000262189.10:c.13106G>T	ENSP00000262189.6:p.Gly4369Val
ENST00000355193.6:c.13106G>T	ENSP00000347325.3:p.Gly4369Val
ENST00000360104.7:c.5787G>T
ENST00000424877.5:c.2957G>T	ENSP00000410411.1:p.Gly986Val
ENST00000473186.5:n.10988G>T
ENST00000558084.5:c.*10626G>T	ENSP00000453752.1:n.*10626G>T
NM_170606.2:c.13106G>T	NP_733751.2:p.Gly4369Val
XM_005250025.3:c.13322G>T	XP_005250082.1:p.Gly4441Val
XM_005250026.2:c.13319G>T	XP_005250083.1:p.Gly4440Val
XM_005250027.3:c.13319G>T	XP_005250084.1:p.Gly4440Val
XM_005250028.3:c.13322G>T	XP_005250085.1:p.Gly4441Val
XM_005250031.3:c.13157G>T	XP_005250088.1:p.Gly4386Val
XM_006716077.2:c.13319G>T	XP_006716140.1:p.Gly4440Val
XM_006716078.2:c.13250G>T	XP_006716141.1:p.Gly4417Val
XM_006716079.2:c.13154G>T	XP_006716142.1:p.Gly4385Val
XM_011516450.1:c.13274G>T	XP_011514752.1:p.Gly4425Val
XM_011516451.1:c.13202G>T	XP_011514753.1:p.Gly4401Val
XM_011516452.1:c.13169G>T	XP_011514754.1:p.Gly4390Val
XM_011516453.1:c.13085G>T	XP_011514755.1:p.Gly4362Val
XM_011516454.1:c.12407G>T	XP_011514756.1:p.Gly4136Val
XM_011516455.1:c.10868G>T	XP_011514757.1:p.Gly3623Val
XM_011516456.1:c.13274G>T	XP_011514758.1:p.Gly4425Val
XM_005250025.4:c.13322G>T	XP_005250082.1:p.Gly4441Val
XM_005250026.3:c.13319G>T	XP_005250083.1:p.Gly4440Val
XM_005250027.4:c.13319G>T	XP_005250084.1:p.Gly4440Val
XM_005250028.4:c.13322G>T	XP_005250085.1:p.Gly4441Val
XM_005250031.4:c.13157G>T	XP_005250088.1:p.Gly4386Val
XM_006716077.3:c.13319G>T	XP_006716140.1:p.Gly4440Val
XM_006716078.3:c.13250G>T	XP_006716141.1:p.Gly4417Val
XM_006716079.3:c.13154G>T	XP_006716142.1:p.Gly4385Val
XM_011516450.2:c.13274G>T	XP_011514752.1:p.Gly4425Val
XM_011516451.2:c.13202G>T	XP_011514753.1:p.Gly4401Val
XM_011516452.2:c.13169G>T	XP_011514754.1:p.Gly4390Val
XM_011516453.2:c.13085G>T	XP_011514755.1:p.Gly4362Val
XM_011516454.2:c.12407G>T	XP_011514756.1:p.Gly4136Val
XM_011516456.2:c.13274G>T	XP_011514758.1:p.Gly4425Val
XM_017012480.1:c.13322G>T	XP_016867969.1:p.Gly4441Val
XM_017012481.1:c.13319G>T	XP_016867970.1:p.Gly4440Val
XM_017012482.1:c.13319G>T	XP_016867971.1:p.Gly4440Val
XM_017012483.1:c.13319G>T	XP_016867972.1:p.Gly4440Val
XM_017012484.1:c.13289G>T	XP_016867973.1:p.Gly4430Val
XM_017012485.1:c.13271G>T	XP_016867974.1:p.Gly4424Val
XM_017012486.1:c.13247G>T	XP_016867975.1:p.Gly4416Val
XM_017012487.1:c.13175G>T	XP_016867976.1:p.Gly4392Val
XM_017012488.1:c.13139G>T	XP_016867977.1:p.Gly4380Val
XM_017012489.1:c.9992G>T	XP_016867978.1:p.Gly3331Val
XM_017012490.2:c.9596G>T	XP_016867979.1:p.Gly3199Val
XM_024446852.1:c.13319G>T	XP_024302620.1:p.Gly4440Val
XM_024446853.1:c.13247G>T	XP_024302621.1:p.Gly4416Val
NM_170606.3:c.13106G>T MANE Select	NP_733751.2:p.Gly4369Val