Canonical Allele Identifier: CA375794479

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707951T>G (hg19) ; chr9:g.137813499T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813499T>G , CM000671.2:g.137813499T>G	GRCh38
NC_000009.11:g.140707951T>G , CM000671.1:g.140707951T>G	GRCh37
NC_000009.10:g.139827772T>G	NCBI36
NG_011776.1:g.199508T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3149T>G MANE Select	ENSP00000417980.1:p.Met1050Arg
ENST00000637161.1:c.3056T>G	ENSP00000490328.1:p.Met1019Arg
ENST00000637261.1:c.3189T>G	ENSP00000490815.1:n.3189T>G
ENST00000637891.1:c.1043T>G	ENSP00000490907.1:p.Met348Arg
ENST00000460843.5:c.3149T>G	ENSP00000417980.1:p.Met1050Arg
ENST00000462942.3:c.2006T>G	ENSP00000436107.1:p.Met669Arg
ENST00000483653.1:n.9T>G
ENST00000488242.2:n.675T>G
NM_024757.4:c.3149T>G	NP_079033.4:p.Met1050Arg
XM_005266105.3:c.3140T>G	XP_005266162.1:p.Met1047Arg
XM_005266110.1:c.3056T>G	XP_005266167.1:p.Met1019Arg
XM_006717288.2:c.3131T>G	XP_006717351.1:p.Met1044Arg
XM_011519021.1:c.3158T>G	XP_011517323.1:p.Met1053Arg
XM_011519022.1:c.3155T>G	XP_011517324.1:p.Met1052Arg
XM_011519023.1:c.3137T>G	XP_011517325.1:p.Met1046Arg
XM_011519024.1:c.3080T>G	XP_011517326.1:p.Met1027Arg
XM_011519025.1:c.3056T>G	XP_011517327.1:p.Met1019Arg
XM_011519026.1:c.3014T>G	XP_011517328.1:p.Met1005Arg
XM_011519029.1:c.1580T>G	XP_011517331.1:p.Met527Arg
XM_011519030.1:c.932T>G	XP_011517332.1:p.Met311Arg
XM_011519031.1:c.719T>G	XP_011517333.1:p.Met240Arg
XM_011519032.1:c.719T>G	XP_011517334.1:p.Met240Arg
XM_011519033.1:c.2993T>G	XP_011517335.1:p.Met998Arg
NM_001354263.1:c.3128T>G	NP_001341192.1:p.Met1043Arg
XM_005266105.5:c.3140T>G	XP_005266162.1:p.Met1047Arg
XM_011519021.3:c.3158T>G	XP_011517323.1:p.Met1053Arg
XM_011519022.3:c.3155T>G	XP_011517324.1:p.Met1052Arg
XM_011519023.3:c.3137T>G	XP_011517325.1:p.Met1046Arg
XM_011519029.3:c.1580T>G	XP_011517331.1:p.Met527Arg
XM_011519030.3:c.932T>G	XP_011517332.1:p.Met311Arg
XM_017015134.1:c.3134T>G	XP_016870623.1:p.Met1045Arg
XM_017015136.2:c.3050T>G	XP_016870625.1:p.Met1017Arg
XM_017015137.1:c.3035T>G	XP_016870626.1:p.Met1012Arg
XM_017015138.1:c.3035T>G	XP_016870627.1:p.Met1012Arg
XM_024447674.1:c.2978T>G	XP_024303442.1:p.Met993Arg
XM_024447675.1:c.2912T>G	XP_024303443.1:p.Met971Arg
XM_024447676.1:c.2273T>G	XP_024303444.1:p.Met758Arg
XM_024447677.1:c.2273T>G	XP_024303445.1:p.Met758Arg
XM_024447680.1:c.2891T>G	XP_024303448.1:p.Met964Arg
NM_024757.5:c.3149T>G MANE Select	NP_079033.4:p.Met1050Arg
NM_001354263.2:c.3128T>G	NP_001341192.1:p.Met1043Arg