Canonical Allele Identifier: CA375773474

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140712536C>G (hg19) ; chr9:g.137818084C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137818084C>G , CM000671.2:g.137818084C>G	GRCh38
NC_000009.11:g.140712536C>G , CM000671.1:g.140712536C>G	GRCh37
NC_000009.10:g.139832357C>G	NCBI36
NG_011776.1:g.204093C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3486C>G MANE Select	ENSP00000417980.1:p.Asp1162Glu
ENST00000636472.1:n.48C>G
ENST00000637161.1:c.3393C>G	ENSP00000490328.1:p.Asp1131Glu
ENST00000637261.1:c.4060C>G	ENSP00000490815.1:n.4060C>G
ENST00000637748.1:n.467C>G
ENST00000637891.1:c.1560C>G	ENSP00000490907.1:n.1560C>G
ENST00000460843.5:c.3486C>G	ENSP00000417980.1:p.Asp1162Glu
ENST00000462942.3:c.2343C>G	ENSP00000436107.1:p.Asp781Glu
ENST00000475564.5:n.1210C>G
ENST00000494249.5:n.839C>G
NM_024757.4:c.3486C>G	NP_079033.4:p.Asp1162Glu
XM_005266105.3:c.3477C>G	XP_005266162.1:p.Asp1159Glu
XM_005266110.1:c.3393C>G	XP_005266167.1:p.Asp1131Glu
XM_006717288.2:c.3468C>G	XP_006717351.1:p.Asp1156Glu
XM_011519021.1:c.3495C>G	XP_011517323.1:p.Asp1165Glu
XM_011519022.1:c.3492C>G	XP_011517324.1:p.Asp1164Glu
XM_011519023.1:c.3474C>G	XP_011517325.1:p.Asp1158Glu
XM_011519024.1:c.3417C>G	XP_011517326.1:p.Asp1139Glu
XM_011519025.1:c.3393C>G	XP_011517327.1:p.Asp1131Glu
XM_011519026.1:c.3351C>G	XP_011517328.1:p.Asp1117Glu
XM_011519029.1:c.1917C>G	XP_011517331.1:p.Asp639Glu
XM_011519030.1:c.1269C>G	XP_011517332.1:p.Asp423Glu
XM_011519031.1:c.1056C>G	XP_011517333.1:p.Asp352Glu
XM_011519032.1:c.1056C>G	XP_011517334.1:p.Asp352Glu
XM_011519033.1:c.3330C>G	XP_011517335.1:p.Asp1110Glu
XR_930459.1:n.5297-3522G>C
NM_001354263.1:c.3465C>G	NP_001341192.1:p.Asp1155Glu
XM_005266105.5:c.3477C>G	XP_005266162.1:p.Asp1159Glu
XM_011519021.3:c.3495C>G	XP_011517323.1:p.Asp1165Glu
XM_011519022.3:c.3492C>G	XP_011517324.1:p.Asp1164Glu
XM_011519023.3:c.3474C>G	XP_011517325.1:p.Asp1158Glu
XM_011519029.3:c.1917C>G	XP_011517331.1:p.Asp639Glu
XM_011519030.3:c.1269C>G	XP_011517332.1:p.Asp423Glu
XM_017015134.1:c.3471C>G	XP_016870623.1:p.Asp1157Glu
XM_017015136.2:c.3387C>G	XP_016870625.1:p.Asp1129Glu
XM_017015137.1:c.3372C>G	XP_016870626.1:p.Asp1124Glu
XM_017015138.1:c.3372C>G	XP_016870627.1:p.Asp1124Glu
XM_024447674.1:c.3315C>G	XP_024303442.1:p.Asp1105Glu
XM_024447675.1:c.3249C>G	XP_024303443.1:p.Asp1083Glu
XM_024447676.1:c.2610C>G	XP_024303444.1:p.Asp870Glu
XM_024447677.1:c.2610C>G	XP_024303445.1:p.Asp870Glu
XM_024447680.1:c.3228C>G	XP_024303448.1:p.Asp1076Glu
NM_024757.5:c.3486C>G MANE Select	NP_079033.4:p.Asp1162Glu
NM_001354263.2:c.3465C>G	NP_001341192.1:p.Asp1155Glu