Canonical Allele Identifier: CA458885055

Gene: KMT2C

Linked Data

• dbSNP Id: rs2091364636
• MyVariant Identifiers: chr7:g.151845803G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148718G>A , CM000669.2:g.152148718G>A	GRCh38
NC_000007.13:g.151845803G>A , CM000669.1:g.151845803G>A	GRCh37
NC_000007.12:g.151476736G>A	NCBI36
NG_033948.1:g.292288C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1397C>T
ENST00000682116.1:n.2341C>T
ENST00000682283.1:c.13380C>T	ENSP00000507485.1:p.Cys4460=
ENST00000682629.1:n.2509C>T
ENST00000683120.1:n.8401C>T
ENST00000683178.1:c.3782C>T
ENST00000683200.1:c.10719C>T	ENSP00000508052.1:p.Cys3573=
ENST00000683337.1:n.4839C>T
ENST00000683502.1:c.3854C>T
ENST00000683621.1:n.1975C>T
ENST00000683640.1:n.1925C>T
ENST00000684069.1:c.1626C>T	ENSP00000507650.1:p.Cys542=
ENST00000684261.1:c.8106C>T	ENSP00000508097.1:p.Cys2702=
ENST00000684649.1:c.3854C>T
ENST00000262189.11:c.13209C>T MANE Select	ENSP00000262189.6:p.Cys4403=
ENST00000360104.8:c.8996C>T
ENST00000418061.2:c.3851C>T
ENST00000424877.6:c.3785C>T
ENST00000679393.1:n.7920C>T
ENST00000679560.1:c.8109C>T	ENSP00000505094.1:p.Cys2703=
ENST00000679882.1:c.12774C>T	ENSP00000506154.1:p.Cys4258=
ENST00000680029.1:c.3786C>T
ENST00000680877.1:c.8109C>T	ENSP00000505724.1:p.Cys2703=
ENST00000681923.1:n.2224C>T
ENST00000262189.10:c.13209C>T	ENSP00000262189.6:p.Cys4403=
ENST00000355193.6:c.13209C>T	ENSP00000347325.3:p.Cys4403=
ENST00000360104.7:c.5890C>T
ENST00000424877.5:c.3060C>T	ENSP00000410411.1:p.Cys1020=
ENST00000473186.5:n.11091C>T
ENST00000558084.5:c.*10729C>T	ENSP00000453752.1:n.*10729C>T
NM_170606.2:c.13209C>T	NP_733751.2:p.Cys4403=
XM_005250025.3:c.13425C>T	XP_005250082.1:p.Cys4475=
XM_005250026.2:c.13422C>T	XP_005250083.1:p.Cys4474=
XM_005250027.3:c.13422C>T	XP_005250084.1:p.Cys4474=
XM_005250028.3:c.13425C>T	XP_005250085.1:p.Cys4475=
XM_005250031.3:c.13260C>T	XP_005250088.1:p.Cys4420=
XM_006716077.2:c.13422C>T	XP_006716140.1:p.Cys4474=
XM_006716078.2:c.13353C>T	XP_006716141.1:p.Cys4451=
XM_006716079.2:c.13257C>T	XP_006716142.1:p.Cys4419=
XM_011516450.1:c.13377C>T	XP_011514752.1:p.Cys4459=
XM_011516451.1:c.13305C>T	XP_011514753.1:p.Cys4435=
XM_011516452.1:c.13272C>T	XP_011514754.1:p.Cys4424=
XM_011516453.1:c.13188C>T	XP_011514755.1:p.Cys4396=
XM_011516454.1:c.12510C>T	XP_011514756.1:p.Cys4170=
XM_011516455.1:c.10971C>T	XP_011514757.1:p.Cys3657=
XM_011516456.1:c.13377C>T	XP_011514758.1:p.Cys4459=
XM_005250025.4:c.13425C>T	XP_005250082.1:p.Cys4475=
XM_005250026.3:c.13422C>T	XP_005250083.1:p.Cys4474=
XM_005250027.4:c.13422C>T	XP_005250084.1:p.Cys4474=
XM_005250028.4:c.13425C>T	XP_005250085.1:p.Cys4475=
XM_005250031.4:c.13260C>T	XP_005250088.1:p.Cys4420=
XM_006716077.3:c.13422C>T	XP_006716140.1:p.Cys4474=
XM_006716078.3:c.13353C>T	XP_006716141.1:p.Cys4451=
XM_006716079.3:c.13257C>T	XP_006716142.1:p.Cys4419=
XM_011516450.2:c.13377C>T	XP_011514752.1:p.Cys4459=
XM_011516451.2:c.13305C>T	XP_011514753.1:p.Cys4435=
XM_011516452.2:c.13272C>T	XP_011514754.1:p.Cys4424=
XM_011516453.2:c.13188C>T	XP_011514755.1:p.Cys4396=
XM_011516454.2:c.12510C>T	XP_011514756.1:p.Cys4170=
XM_011516456.2:c.13377C>T	XP_011514758.1:p.Cys4459=
XM_017012480.1:c.13425C>T	XP_016867969.1:p.Cys4475=
XM_017012481.1:c.13422C>T	XP_016867970.1:p.Cys4474=
XM_017012482.1:c.13422C>T	XP_016867971.1:p.Cys4474=
XM_017012483.1:c.13422C>T	XP_016867972.1:p.Cys4474=
XM_017012484.1:c.13392C>T	XP_016867973.1:p.Cys4464=
XM_017012485.1:c.13374C>T	XP_016867974.1:p.Cys4458=
XM_017012486.1:c.13350C>T	XP_016867975.1:p.Cys4450=
XM_017012487.1:c.13278C>T	XP_016867976.1:p.Cys4426=
XM_017012488.1:c.13242C>T	XP_016867977.1:p.Cys4414=
XM_017012489.1:c.10095C>T	XP_016867978.1:p.Cys3365=
XM_017012490.2:c.9699C>T	XP_016867979.1:p.Cys3233=
XM_024446852.1:c.13422C>T	XP_024302620.1:p.Cys4474=
XM_024446853.1:c.13350C>T	XP_024302621.1:p.Cys4450=
NM_170606.3:c.13209C>T MANE Select	NP_733751.2:p.Cys4403=