Canonical Allele Identifier: CA375788726

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695341G>C (hg19) ; chr9:g.137800889G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800889G>C , CM000671.2:g.137800889G>C	GRCh38
NC_000009.11:g.140695341G>C , CM000671.1:g.140695341G>C	GRCh37
NC_000009.10:g.139815162G>C	NCBI36
NG_011776.1:g.186898G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2617G>C MANE Select	ENSP00000417980.1:p.Gly873Arg
ENST00000636027.1:c.2503G>C	ENSP00000489961.1:p.Gly835Arg
ENST00000637161.1:c.2524G>C	ENSP00000490328.1:p.Gly842Arg
ENST00000637261.1:c.2657G>C	ENSP00000490815.1:n.2657G>C
ENST00000637891.1:c.511G>C	ENSP00000490907.1:p.Gly171Arg
ENST00000637949.1:c.295G>C	ENSP00000489786.1:p.Gly99Arg
ENST00000460843.5:c.2617G>C	ENSP00000417980.1:p.Gly873Arg
ENST00000462942.3:c.1474G>C	ENSP00000436107.1:p.Gly492Arg
ENST00000482340.5:c.187G>C	ENSP00000486748.1:p.Gly63Arg
ENST00000486164.5:c.195G>C
ENST00000488242.2:n.143G>C
ENST00000493484.5:c.187G>C	ENSP00000486503.1:p.Gly63Arg
NM_024757.4:c.2617G>C	NP_079033.4:p.Gly873Arg
XM_005266105.3:c.2608G>C	XP_005266162.1:p.Gly870Arg
XM_005266110.1:c.2524G>C	XP_005266167.1:p.Gly842Arg
XM_006717288.2:c.2599G>C	XP_006717351.1:p.Gly867Arg
XM_011519021.1:c.2626G>C	XP_011517323.1:p.Gly876Arg
XM_011519022.1:c.2623G>C	XP_011517324.1:p.Gly875Arg
XM_011519023.1:c.2605G>C	XP_011517325.1:p.Gly869Arg
XM_011519024.1:c.2548G>C	XP_011517326.1:p.Gly850Arg
XM_011519025.1:c.2524G>C	XP_011517327.1:p.Gly842Arg
XM_011519026.1:c.2482G>C	XP_011517328.1:p.Gly828Arg
XM_011519027.1:c.2626G>C	XP_011517329.1:p.Gly876Arg
XM_011519029.1:c.1048G>C	XP_011517331.1:p.Gly350Arg
XM_011519030.1:c.400G>C	XP_011517332.1:p.Gly134Arg
XM_011519031.1:c.187G>C	XP_011517333.1:p.Gly63Arg
XM_011519032.1:c.187G>C	XP_011517334.1:p.Gly63Arg
XM_011519033.1:c.2461G>C	XP_011517335.1:p.Gly821Arg
NM_001354263.1:c.2596G>C	NP_001341192.1:p.Gly866Arg
XM_005266105.5:c.2608G>C	XP_005266162.1:p.Gly870Arg
XM_011519021.3:c.2626G>C	XP_011517323.1:p.Gly876Arg
XM_011519022.3:c.2623G>C	XP_011517324.1:p.Gly875Arg
XM_011519023.3:c.2605G>C	XP_011517325.1:p.Gly869Arg
XM_011519029.3:c.1048G>C	XP_011517331.1:p.Gly350Arg
XM_011519030.3:c.400G>C	XP_011517332.1:p.Gly134Arg
XM_017015134.1:c.2602G>C	XP_016870623.1:p.Gly868Arg
XM_017015136.2:c.2518G>C	XP_016870625.1:p.Gly840Arg
XM_017015137.1:c.2503G>C	XP_016870626.1:p.Gly835Arg
XM_017015138.1:c.2503G>C	XP_016870627.1:p.Gly835Arg
XM_024447674.1:c.2446G>C	XP_024303442.1:p.Gly816Arg
XM_024447675.1:c.2380G>C	XP_024303443.1:p.Gly794Arg
XM_024447676.1:c.1741G>C	XP_024303444.1:p.Gly581Arg
XM_024447677.1:c.1741G>C	XP_024303445.1:p.Gly581Arg
XM_024447678.1:c.2524G>C	XP_024303446.1:p.Gly842Arg
XM_024447680.1:c.2359G>C	XP_024303448.1:p.Gly787Arg
NM_024757.5:c.2617G>C MANE Select	NP_079033.4:p.Gly873Arg
NM_001354263.2:c.2596G>C	NP_001341192.1:p.Gly866Arg