Canonical Allele Identifier: CA375773905

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140712578T>G (hg19) ; chr9:g.137818126T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137818126T>G , CM000671.2:g.137818126T>G	GRCh38
NC_000009.11:g.140712578T>G , CM000671.1:g.140712578T>G	GRCh37
NC_000009.10:g.139832399T>G	NCBI36
NG_011776.1:g.204135T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3528T>G MANE Select	ENSP00000417980.1:p.Asp1176Glu
ENST00000636472.1:n.90T>G
ENST00000636526.1:n.14T>G
ENST00000637161.1:c.3435T>G	ENSP00000490328.1:p.Asp1145Glu
ENST00000637261.1:c.4102T>G	ENSP00000490815.1:n.4102T>G
ENST00000637748.1:n.509T>G
ENST00000637891.1:c.1602T>G	ENSP00000490907.1:n.1602T>G
ENST00000460843.5:c.3528T>G	ENSP00000417980.1:p.Asp1176Glu
ENST00000462942.3:c.2385T>G	ENSP00000436107.1:p.Asp795Glu
ENST00000475564.5:n.1252T>G
ENST00000494249.5:n.881T>G
NM_024757.4:c.3528T>G	NP_079033.4:p.Asp1176Glu
XM_005266105.3:c.3519T>G	XP_005266162.1:p.Asp1173Glu
XM_005266110.1:c.3435T>G	XP_005266167.1:p.Asp1145Glu
XM_006717288.2:c.3510T>G	XP_006717351.1:p.Asp1170Glu
XM_011519021.1:c.3537T>G	XP_011517323.1:p.Asp1179Glu
XM_011519022.1:c.3534T>G	XP_011517324.1:p.Asp1178Glu
XM_011519023.1:c.3516T>G	XP_011517325.1:p.Asp1172Glu
XM_011519024.1:c.3459T>G	XP_011517326.1:p.Asp1153Glu
XM_011519025.1:c.3435T>G	XP_011517327.1:p.Asp1145Glu
XM_011519026.1:c.3393T>G	XP_011517328.1:p.Asp1131Glu
XM_011519029.1:c.1959T>G	XP_011517331.1:p.Asp653Glu
XM_011519030.1:c.1311T>G	XP_011517332.1:p.Asp437Glu
XM_011519031.1:c.1098T>G	XP_011517333.1:p.Asp366Glu
XM_011519032.1:c.1098T>G	XP_011517334.1:p.Asp366Glu
XM_011519033.1:c.3372T>G	XP_011517335.1:p.Asp1124Glu
XR_930459.1:n.5297-3564A>C
NM_001354263.1:c.3507T>G	NP_001341192.1:p.Asp1169Glu
XM_005266105.5:c.3519T>G	XP_005266162.1:p.Asp1173Glu
XM_011519021.3:c.3537T>G	XP_011517323.1:p.Asp1179Glu
XM_011519022.3:c.3534T>G	XP_011517324.1:p.Asp1178Glu
XM_011519023.3:c.3516T>G	XP_011517325.1:p.Asp1172Glu
XM_011519029.3:c.1959T>G	XP_011517331.1:p.Asp653Glu
XM_011519030.3:c.1311T>G	XP_011517332.1:p.Asp437Glu
XM_017015134.1:c.3513T>G	XP_016870623.1:p.Asp1171Glu
XM_017015136.2:c.3429T>G	XP_016870625.1:p.Asp1143Glu
XM_017015137.1:c.3414T>G	XP_016870626.1:p.Asp1138Glu
XM_017015138.1:c.3414T>G	XP_016870627.1:p.Asp1138Glu
XM_024447674.1:c.3357T>G	XP_024303442.1:p.Asp1119Glu
XM_024447675.1:c.3291T>G	XP_024303443.1:p.Asp1097Glu
XM_024447676.1:c.2652T>G	XP_024303444.1:p.Asp884Glu
XM_024447677.1:c.2652T>G	XP_024303445.1:p.Asp884Glu
XM_024447680.1:c.3270T>G	XP_024303448.1:p.Asp1090Glu
NM_024757.5:c.3528T>G MANE Select	NP_079033.4:p.Asp1176Glu
NM_001354263.2:c.3507T>G	NP_001341192.1:p.Asp1169Glu