Canonical Allele Identifier: CA370092930

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845837G>T (hg19) ; chr7:g.152148752G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148752G>T , CM000669.2:g.152148752G>T	GRCh38
NC_000007.13:g.151845837G>T , CM000669.1:g.151845837G>T	GRCh37
NC_000007.12:g.151476770G>T	NCBI36
NG_033948.1:g.292254C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1363C>A
ENST00000682116.1:n.2307C>A
ENST00000682283.1:c.13346C>A	ENSP00000507485.1:p.Pro4449His
ENST00000682629.1:n.2475C>A
ENST00000683120.1:n.8367C>A
ENST00000683178.1:c.3748C>A
ENST00000683200.1:c.10685C>A	ENSP00000508052.1:p.Pro3562His
ENST00000683337.1:n.4805C>A
ENST00000683502.1:c.3820C>A
ENST00000683621.1:n.1941C>A
ENST00000683640.1:n.1891C>A
ENST00000684069.1:c.1592C>A	ENSP00000507650.1:p.Pro531His
ENST00000684261.1:c.8072C>A	ENSP00000508097.1:p.Pro2691His
ENST00000684649.1:c.3820C>A
ENST00000262189.11:c.13175C>A MANE Select	ENSP00000262189.6:p.Pro4392His
ENST00000360104.8:c.8962C>A
ENST00000418061.2:c.3817C>A
ENST00000424877.6:c.3751C>A
ENST00000679393.1:n.7886C>A
ENST00000679560.1:c.8075C>A	ENSP00000505094.1:p.Pro2692His
ENST00000679882.1:c.12740C>A	ENSP00000506154.1:p.Pro4247His
ENST00000680029.1:c.3752C>A
ENST00000680877.1:c.8075C>A	ENSP00000505724.1:p.Pro2692His
ENST00000681923.1:n.2190C>A
ENST00000262189.10:c.13175C>A	ENSP00000262189.6:p.Pro4392His
ENST00000355193.6:c.13175C>A	ENSP00000347325.3:p.Pro4392His
ENST00000360104.7:c.5856C>A
ENST00000424877.5:c.3026C>A	ENSP00000410411.1:p.Pro1009His
ENST00000473186.5:n.11057C>A
ENST00000558084.5:c.*10695C>A	ENSP00000453752.1:n.*10695C>A
NM_170606.2:c.13175C>A	NP_733751.2:p.Pro4392His
XM_005250025.3:c.13391C>A	XP_005250082.1:p.Pro4464His
XM_005250026.2:c.13388C>A	XP_005250083.1:p.Pro4463His
XM_005250027.3:c.13388C>A	XP_005250084.1:p.Pro4463His
XM_005250028.3:c.13391C>A	XP_005250085.1:p.Pro4464His
XM_005250031.3:c.13226C>A	XP_005250088.1:p.Pro4409His
XM_006716077.2:c.13388C>A	XP_006716140.1:p.Pro4463His
XM_006716078.2:c.13319C>A	XP_006716141.1:p.Pro4440His
XM_006716079.2:c.13223C>A	XP_006716142.1:p.Pro4408His
XM_011516450.1:c.13343C>A	XP_011514752.1:p.Pro4448His
XM_011516451.1:c.13271C>A	XP_011514753.1:p.Pro4424His
XM_011516452.1:c.13238C>A	XP_011514754.1:p.Pro4413His
XM_011516453.1:c.13154C>A	XP_011514755.1:p.Pro4385His
XM_011516454.1:c.12476C>A	XP_011514756.1:p.Pro4159His
XM_011516455.1:c.10937C>A	XP_011514757.1:p.Pro3646His
XM_011516456.1:c.13343C>A	XP_011514758.1:p.Pro4448His
XM_005250025.4:c.13391C>A	XP_005250082.1:p.Pro4464His
XM_005250026.3:c.13388C>A	XP_005250083.1:p.Pro4463His
XM_005250027.4:c.13388C>A	XP_005250084.1:p.Pro4463His
XM_005250028.4:c.13391C>A	XP_005250085.1:p.Pro4464His
XM_005250031.4:c.13226C>A	XP_005250088.1:p.Pro4409His
XM_006716077.3:c.13388C>A	XP_006716140.1:p.Pro4463His
XM_006716078.3:c.13319C>A	XP_006716141.1:p.Pro4440His
XM_006716079.3:c.13223C>A	XP_006716142.1:p.Pro4408His
XM_011516450.2:c.13343C>A	XP_011514752.1:p.Pro4448His
XM_011516451.2:c.13271C>A	XP_011514753.1:p.Pro4424His
XM_011516452.2:c.13238C>A	XP_011514754.1:p.Pro4413His
XM_011516453.2:c.13154C>A	XP_011514755.1:p.Pro4385His
XM_011516454.2:c.12476C>A	XP_011514756.1:p.Pro4159His
XM_011516456.2:c.13343C>A	XP_011514758.1:p.Pro4448His
XM_017012480.1:c.13391C>A	XP_016867969.1:p.Pro4464His
XM_017012481.1:c.13388C>A	XP_016867970.1:p.Pro4463His
XM_017012482.1:c.13388C>A	XP_016867971.1:p.Pro4463His
XM_017012483.1:c.13388C>A	XP_016867972.1:p.Pro4463His
XM_017012484.1:c.13358C>A	XP_016867973.1:p.Pro4453His
XM_017012485.1:c.13340C>A	XP_016867974.1:p.Pro4447His
XM_017012486.1:c.13316C>A	XP_016867975.1:p.Pro4439His
XM_017012487.1:c.13244C>A	XP_016867976.1:p.Pro4415His
XM_017012488.1:c.13208C>A	XP_016867977.1:p.Pro4403His
XM_017012489.1:c.10061C>A	XP_016867978.1:p.Pro3354His
XM_017012490.2:c.9665C>A	XP_016867979.1:p.Pro3222His
XM_024446852.1:c.13388C>A	XP_024302620.1:p.Pro4463His
XM_024446853.1:c.13316C>A	XP_024302621.1:p.Pro4439His
NM_170606.3:c.13175C>A MANE Select	NP_733751.2:p.Pro4392His