Canonical Allele Identifier: CA370093201

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845918A>C (hg19) ; chr7:g.152148833A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148833A>C , CM000669.2:g.152148833A>C	GRCh38
NC_000007.13:g.151845918A>C , CM000669.1:g.151845918A>C	GRCh37
NC_000007.12:g.151476851A>C	NCBI36
NG_033948.1:g.292173T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1282T>G
ENST00000682116.1:n.2226T>G
ENST00000682283.1:c.13265T>G	ENSP00000507485.1:p.Val4422Gly
ENST00000682629.1:n.2394T>G
ENST00000683120.1:n.8286T>G
ENST00000683178.1:c.3667T>G
ENST00000683200.1:c.10604T>G	ENSP00000508052.1:p.Val3535Gly
ENST00000683337.1:n.4724T>G
ENST00000683502.1:c.3739T>G
ENST00000683621.1:n.1860T>G
ENST00000683640.1:n.1810T>G
ENST00000684069.1:c.1511T>G	ENSP00000507650.1:p.Val504Gly
ENST00000684261.1:c.7991T>G	ENSP00000508097.1:p.Val2664Gly
ENST00000684649.1:c.3739T>G
ENST00000262189.11:c.13094T>G MANE Select	ENSP00000262189.6:p.Val4365Gly
ENST00000360104.8:c.8881T>G
ENST00000418061.2:c.3736T>G
ENST00000424877.6:c.3670T>G
ENST00000679393.1:n.7805T>G
ENST00000679560.1:c.7994T>G	ENSP00000505094.1:p.Val2665Gly
ENST00000679882.1:c.12659T>G	ENSP00000506154.1:p.Val4220Gly
ENST00000680029.1:c.3671T>G
ENST00000680877.1:c.7994T>G	ENSP00000505724.1:p.Val2665Gly
ENST00000681923.1:n.2109T>G
ENST00000262189.10:c.13094T>G	ENSP00000262189.6:p.Val4365Gly
ENST00000355193.6:c.13094T>G	ENSP00000347325.3:p.Val4365Gly
ENST00000360104.7:c.5775T>G
ENST00000424877.5:c.2945T>G	ENSP00000410411.1:p.Val982Gly
ENST00000473186.5:n.10976T>G
ENST00000558084.5:c.*10614T>G	ENSP00000453752.1:n.*10614T>G
NM_170606.2:c.13094T>G	NP_733751.2:p.Val4365Gly
XM_005250025.3:c.13310T>G	XP_005250082.1:p.Val4437Gly
XM_005250026.2:c.13307T>G	XP_005250083.1:p.Val4436Gly
XM_005250027.3:c.13307T>G	XP_005250084.1:p.Val4436Gly
XM_005250028.3:c.13310T>G	XP_005250085.1:p.Val4437Gly
XM_005250031.3:c.13145T>G	XP_005250088.1:p.Val4382Gly
XM_006716077.2:c.13307T>G	XP_006716140.1:p.Val4436Gly
XM_006716078.2:c.13238T>G	XP_006716141.1:p.Val4413Gly
XM_006716079.2:c.13142T>G	XP_006716142.1:p.Val4381Gly
XM_011516450.1:c.13262T>G	XP_011514752.1:p.Val4421Gly
XM_011516451.1:c.13190T>G	XP_011514753.1:p.Val4397Gly
XM_011516452.1:c.13157T>G	XP_011514754.1:p.Val4386Gly
XM_011516453.1:c.13073T>G	XP_011514755.1:p.Val4358Gly
XM_011516454.1:c.12395T>G	XP_011514756.1:p.Val4132Gly
XM_011516455.1:c.10856T>G	XP_011514757.1:p.Val3619Gly
XM_011516456.1:c.13262T>G	XP_011514758.1:p.Val4421Gly
XM_005250025.4:c.13310T>G	XP_005250082.1:p.Val4437Gly
XM_005250026.3:c.13307T>G	XP_005250083.1:p.Val4436Gly
XM_005250027.4:c.13307T>G	XP_005250084.1:p.Val4436Gly
XM_005250028.4:c.13310T>G	XP_005250085.1:p.Val4437Gly
XM_005250031.4:c.13145T>G	XP_005250088.1:p.Val4382Gly
XM_006716077.3:c.13307T>G	XP_006716140.1:p.Val4436Gly
XM_006716078.3:c.13238T>G	XP_006716141.1:p.Val4413Gly
XM_006716079.3:c.13142T>G	XP_006716142.1:p.Val4381Gly
XM_011516450.2:c.13262T>G	XP_011514752.1:p.Val4421Gly
XM_011516451.2:c.13190T>G	XP_011514753.1:p.Val4397Gly
XM_011516452.2:c.13157T>G	XP_011514754.1:p.Val4386Gly
XM_011516453.2:c.13073T>G	XP_011514755.1:p.Val4358Gly
XM_011516454.2:c.12395T>G	XP_011514756.1:p.Val4132Gly
XM_011516456.2:c.13262T>G	XP_011514758.1:p.Val4421Gly
XM_017012480.1:c.13310T>G	XP_016867969.1:p.Val4437Gly
XM_017012481.1:c.13307T>G	XP_016867970.1:p.Val4436Gly
XM_017012482.1:c.13307T>G	XP_016867971.1:p.Val4436Gly
XM_017012483.1:c.13307T>G	XP_016867972.1:p.Val4436Gly
XM_017012484.1:c.13277T>G	XP_016867973.1:p.Val4426Gly
XM_017012485.1:c.13259T>G	XP_016867974.1:p.Val4420Gly
XM_017012486.1:c.13235T>G	XP_016867975.1:p.Val4412Gly
XM_017012487.1:c.13163T>G	XP_016867976.1:p.Val4388Gly
XM_017012488.1:c.13127T>G	XP_016867977.1:p.Val4376Gly
XM_017012489.1:c.9980T>G	XP_016867978.1:p.Val3327Gly
XM_017012490.2:c.9584T>G	XP_016867979.1:p.Val3195Gly
XM_024446852.1:c.13307T>G	XP_024302620.1:p.Val4436Gly
XM_024446853.1:c.13235T>G	XP_024302621.1:p.Val4412Gly
NM_170606.3:c.13094T>G MANE Select	NP_733751.2:p.Val4365Gly