Canonical Allele Identifier: CA458884909

Gene: KMT2C

Linked Data

• gnomAD v4: 7-152148868-T-C
• MyVariant Identifiers: chr7:g.151845953T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148868T>C , CM000669.2:g.152148868T>C	GRCh38
NC_000007.13:g.151845953T>C , CM000669.1:g.151845953T>C	GRCh37
NC_000007.12:g.151476886T>C	NCBI36
NG_033948.1:g.292138A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1247A>G
ENST00000682116.1:n.2191A>G
ENST00000682283.1:c.13230A>G	ENSP00000507485.1:p.Arg4410=
ENST00000682629.1:n.2359A>G
ENST00000683120.1:n.8251A>G
ENST00000683178.1:c.3632A>G
ENST00000683200.1:c.10569A>G	ENSP00000508052.1:p.Arg3523=
ENST00000683337.1:n.4689A>G
ENST00000683502.1:c.3704A>G
ENST00000683621.1:n.1825A>G
ENST00000683640.1:n.1775A>G
ENST00000684069.1:c.1476A>G	ENSP00000507650.1:p.Arg492=
ENST00000684261.1:c.7956A>G	ENSP00000508097.1:p.Arg2652=
ENST00000684649.1:c.3704A>G
ENST00000262189.11:c.13059A>G MANE Select	ENSP00000262189.6:p.Arg4353=
ENST00000360104.8:c.8846A>G
ENST00000418061.2:c.3701A>G
ENST00000424877.6:c.3635A>G
ENST00000679393.1:n.7770A>G
ENST00000679560.1:c.7959A>G	ENSP00000505094.1:p.Arg2653=
ENST00000679882.1:c.12624A>G	ENSP00000506154.1:p.Arg4208=
ENST00000680029.1:c.3636A>G
ENST00000680877.1:c.7959A>G	ENSP00000505724.1:p.Arg2653=
ENST00000681923.1:n.2074A>G
ENST00000262189.10:c.13059A>G	ENSP00000262189.6:p.Arg4353=
ENST00000355193.6:c.13059A>G	ENSP00000347325.3:p.Arg4353=
ENST00000360104.7:c.5740A>G
ENST00000424877.5:c.2910A>G	ENSP00000410411.1:p.Arg970=
ENST00000473186.5:n.10941A>G
ENST00000558084.5:c.*10579A>G	ENSP00000453752.1:n.*10579A>G
NM_170606.2:c.13059A>G	NP_733751.2:p.Arg4353=
XM_005250025.3:c.13275A>G	XP_005250082.1:p.Arg4425=
XM_005250026.2:c.13272A>G	XP_005250083.1:p.Arg4424=
XM_005250027.3:c.13272A>G	XP_005250084.1:p.Arg4424=
XM_005250028.3:c.13275A>G	XP_005250085.1:p.Arg4425=
XM_005250031.3:c.13110A>G	XP_005250088.1:p.Arg4370=
XM_006716077.2:c.13272A>G	XP_006716140.1:p.Arg4424=
XM_006716078.2:c.13203A>G	XP_006716141.1:p.Arg4401=
XM_006716079.2:c.13107A>G	XP_006716142.1:p.Arg4369=
XM_011516450.1:c.13227A>G	XP_011514752.1:p.Arg4409=
XM_011516451.1:c.13155A>G	XP_011514753.1:p.Arg4385=
XM_011516452.1:c.13122A>G	XP_011514754.1:p.Arg4374=
XM_011516453.1:c.13038A>G	XP_011514755.1:p.Arg4346=
XM_011516454.1:c.12360A>G	XP_011514756.1:p.Arg4120=
XM_011516455.1:c.10821A>G	XP_011514757.1:p.Arg3607=
XM_011516456.1:c.13227A>G	XP_011514758.1:p.Arg4409=
XM_005250025.4:c.13275A>G	XP_005250082.1:p.Arg4425=
XM_005250026.3:c.13272A>G	XP_005250083.1:p.Arg4424=
XM_005250027.4:c.13272A>G	XP_005250084.1:p.Arg4424=
XM_005250028.4:c.13275A>G	XP_005250085.1:p.Arg4425=
XM_005250031.4:c.13110A>G	XP_005250088.1:p.Arg4370=
XM_006716077.3:c.13272A>G	XP_006716140.1:p.Arg4424=
XM_006716078.3:c.13203A>G	XP_006716141.1:p.Arg4401=
XM_006716079.3:c.13107A>G	XP_006716142.1:p.Arg4369=
XM_011516450.2:c.13227A>G	XP_011514752.1:p.Arg4409=
XM_011516451.2:c.13155A>G	XP_011514753.1:p.Arg4385=
XM_011516452.2:c.13122A>G	XP_011514754.1:p.Arg4374=
XM_011516453.2:c.13038A>G	XP_011514755.1:p.Arg4346=
XM_011516454.2:c.12360A>G	XP_011514756.1:p.Arg4120=
XM_011516456.2:c.13227A>G	XP_011514758.1:p.Arg4409=
XM_017012480.1:c.13275A>G	XP_016867969.1:p.Arg4425=
XM_017012481.1:c.13272A>G	XP_016867970.1:p.Arg4424=
XM_017012482.1:c.13272A>G	XP_016867971.1:p.Arg4424=
XM_017012483.1:c.13272A>G	XP_016867972.1:p.Arg4424=
XM_017012484.1:c.13242A>G	XP_016867973.1:p.Arg4414=
XM_017012485.1:c.13224A>G	XP_016867974.1:p.Arg4408=
XM_017012486.1:c.13200A>G	XP_016867975.1:p.Arg4400=
XM_017012487.1:c.13128A>G	XP_016867976.1:p.Arg4376=
XM_017012488.1:c.13092A>G	XP_016867977.1:p.Arg4364=
XM_017012489.1:c.9945A>G	XP_016867978.1:p.Arg3315=
XM_017012490.2:c.9549A>G	XP_016867979.1:p.Arg3183=
XM_024446852.1:c.13272A>G	XP_024302620.1:p.Arg4424=
XM_024446853.1:c.13200A>G	XP_024302621.1:p.Arg4400=
NM_170606.3:c.13059A>G MANE Select	NP_733751.2:p.Arg4353=