Canonical Allele Identifier: CA458884809

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845911A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148826A>T , CM000669.2:g.152148826A>T	GRCh38
NC_000007.13:g.151845911A>T , CM000669.1:g.151845911A>T	GRCh37
NC_000007.12:g.151476844A>T	NCBI36
NG_033948.1:g.292180T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1289T>A
ENST00000682116.1:n.2233T>A
ENST00000682283.1:c.13272T>A	ENSP00000507485.1:p.Pro4424=
ENST00000682629.1:n.2401T>A
ENST00000683120.1:n.8293T>A
ENST00000683178.1:c.3674T>A
ENST00000683200.1:c.10611T>A	ENSP00000508052.1:p.Pro3537=
ENST00000683337.1:n.4731T>A
ENST00000683502.1:c.3746T>A
ENST00000683621.1:n.1867T>A
ENST00000683640.1:n.1817T>A
ENST00000684069.1:c.1518T>A	ENSP00000507650.1:p.Pro506=
ENST00000684261.1:c.7998T>A	ENSP00000508097.1:p.Pro2666=
ENST00000684649.1:c.3746T>A
ENST00000262189.11:c.13101T>A MANE Select	ENSP00000262189.6:p.Pro4367=
ENST00000360104.8:c.8888T>A
ENST00000418061.2:c.3743T>A
ENST00000424877.6:c.3677T>A
ENST00000679393.1:n.7812T>A
ENST00000679560.1:c.8001T>A	ENSP00000505094.1:p.Pro2667=
ENST00000679882.1:c.12666T>A	ENSP00000506154.1:p.Pro4222=
ENST00000680029.1:c.3678T>A
ENST00000680877.1:c.8001T>A	ENSP00000505724.1:p.Pro2667=
ENST00000681923.1:n.2116T>A
ENST00000262189.10:c.13101T>A	ENSP00000262189.6:p.Pro4367=
ENST00000355193.6:c.13101T>A	ENSP00000347325.3:p.Pro4367=
ENST00000360104.7:c.5782T>A
ENST00000424877.5:c.2952T>A	ENSP00000410411.1:p.Pro984=
ENST00000473186.5:n.10983T>A
ENST00000558084.5:c.*10621T>A	ENSP00000453752.1:n.*10621T>A
NM_170606.2:c.13101T>A	NP_733751.2:p.Pro4367=
XM_005250025.3:c.13317T>A	XP_005250082.1:p.Pro4439=
XM_005250026.2:c.13314T>A	XP_005250083.1:p.Pro4438=
XM_005250027.3:c.13314T>A	XP_005250084.1:p.Pro4438=
XM_005250028.3:c.13317T>A	XP_005250085.1:p.Pro4439=
XM_005250031.3:c.13152T>A	XP_005250088.1:p.Pro4384=
XM_006716077.2:c.13314T>A	XP_006716140.1:p.Pro4438=
XM_006716078.2:c.13245T>A	XP_006716141.1:p.Pro4415=
XM_006716079.2:c.13149T>A	XP_006716142.1:p.Pro4383=
XM_011516450.1:c.13269T>A	XP_011514752.1:p.Pro4423=
XM_011516451.1:c.13197T>A	XP_011514753.1:p.Pro4399=
XM_011516452.1:c.13164T>A	XP_011514754.1:p.Pro4388=
XM_011516453.1:c.13080T>A	XP_011514755.1:p.Pro4360=
XM_011516454.1:c.12402T>A	XP_011514756.1:p.Pro4134=
XM_011516455.1:c.10863T>A	XP_011514757.1:p.Pro3621=
XM_011516456.1:c.13269T>A	XP_011514758.1:p.Pro4423=
XM_005250025.4:c.13317T>A	XP_005250082.1:p.Pro4439=
XM_005250026.3:c.13314T>A	XP_005250083.1:p.Pro4438=
XM_005250027.4:c.13314T>A	XP_005250084.1:p.Pro4438=
XM_005250028.4:c.13317T>A	XP_005250085.1:p.Pro4439=
XM_005250031.4:c.13152T>A	XP_005250088.1:p.Pro4384=
XM_006716077.3:c.13314T>A	XP_006716140.1:p.Pro4438=
XM_006716078.3:c.13245T>A	XP_006716141.1:p.Pro4415=
XM_006716079.3:c.13149T>A	XP_006716142.1:p.Pro4383=
XM_011516450.2:c.13269T>A	XP_011514752.1:p.Pro4423=
XM_011516451.2:c.13197T>A	XP_011514753.1:p.Pro4399=
XM_011516452.2:c.13164T>A	XP_011514754.1:p.Pro4388=
XM_011516453.2:c.13080T>A	XP_011514755.1:p.Pro4360=
XM_011516454.2:c.12402T>A	XP_011514756.1:p.Pro4134=
XM_011516456.2:c.13269T>A	XP_011514758.1:p.Pro4423=
XM_017012480.1:c.13317T>A	XP_016867969.1:p.Pro4439=
XM_017012481.1:c.13314T>A	XP_016867970.1:p.Pro4438=
XM_017012482.1:c.13314T>A	XP_016867971.1:p.Pro4438=
XM_017012483.1:c.13314T>A	XP_016867972.1:p.Pro4438=
XM_017012484.1:c.13284T>A	XP_016867973.1:p.Pro4428=
XM_017012485.1:c.13266T>A	XP_016867974.1:p.Pro4422=
XM_017012486.1:c.13242T>A	XP_016867975.1:p.Pro4414=
XM_017012487.1:c.13170T>A	XP_016867976.1:p.Pro4390=
XM_017012488.1:c.13134T>A	XP_016867977.1:p.Pro4378=
XM_017012489.1:c.9987T>A	XP_016867978.1:p.Pro3329=
XM_017012490.2:c.9591T>A	XP_016867979.1:p.Pro3197=
XM_024446852.1:c.13314T>A	XP_024302620.1:p.Pro4438=
XM_024446853.1:c.13242T>A	XP_024302621.1:p.Pro4414=
NM_170606.3:c.13101T>A MANE Select	NP_733751.2:p.Pro4367=