Canonical Allele Identifier: CA375773300

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140712516G>A (hg19) ; chr9:g.137818064G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137818064G>A , CM000671.2:g.137818064G>A	GRCh38
NC_000009.11:g.140712516G>A , CM000671.1:g.140712516G>A	GRCh37
NC_000009.10:g.139832337G>A	NCBI36
NG_011776.1:g.204073G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3466G>A MANE Select	ENSP00000417980.1:p.Val1156Ile
ENST00000636472.1:n.28G>A
ENST00000637161.1:c.3373G>A	ENSP00000490328.1:p.Val1125Ile
ENST00000637261.1:c.4040G>A	ENSP00000490815.1:n.4040G>A
ENST00000637748.1:n.447G>A
ENST00000637891.1:c.1540G>A	ENSP00000490907.1:n.1540G>A
ENST00000460843.5:c.3466G>A	ENSP00000417980.1:p.Val1156Ile
ENST00000462942.3:c.2323G>A	ENSP00000436107.1:p.Val775Ile
ENST00000475564.5:n.1190G>A
ENST00000494249.5:n.819G>A
NM_024757.4:c.3466G>A	NP_079033.4:p.Val1156Ile
XM_005266105.3:c.3457G>A	XP_005266162.1:p.Val1153Ile
XM_005266110.1:c.3373G>A	XP_005266167.1:p.Val1125Ile
XM_006717288.2:c.3448G>A	XP_006717351.1:p.Val1150Ile
XM_011519021.1:c.3475G>A	XP_011517323.1:p.Val1159Ile
XM_011519022.1:c.3472G>A	XP_011517324.1:p.Val1158Ile
XM_011519023.1:c.3454G>A	XP_011517325.1:p.Val1152Ile
XM_011519024.1:c.3397G>A	XP_011517326.1:p.Val1133Ile
XM_011519025.1:c.3373G>A	XP_011517327.1:p.Val1125Ile
XM_011519026.1:c.3331G>A	XP_011517328.1:p.Val1111Ile
XM_011519029.1:c.1897G>A	XP_011517331.1:p.Val633Ile
XM_011519030.1:c.1249G>A	XP_011517332.1:p.Val417Ile
XM_011519031.1:c.1036G>A	XP_011517333.1:p.Val346Ile
XM_011519032.1:c.1036G>A	XP_011517334.1:p.Val346Ile
XM_011519033.1:c.3310G>A	XP_011517335.1:p.Val1104Ile
XR_930459.1:n.5297-3502C>T
NM_001354263.1:c.3445G>A	NP_001341192.1:p.Val1149Ile
XM_005266105.5:c.3457G>A	XP_005266162.1:p.Val1153Ile
XM_011519021.3:c.3475G>A	XP_011517323.1:p.Val1159Ile
XM_011519022.3:c.3472G>A	XP_011517324.1:p.Val1158Ile
XM_011519023.3:c.3454G>A	XP_011517325.1:p.Val1152Ile
XM_011519029.3:c.1897G>A	XP_011517331.1:p.Val633Ile
XM_011519030.3:c.1249G>A	XP_011517332.1:p.Val417Ile
XM_017015134.1:c.3451G>A	XP_016870623.1:p.Val1151Ile
XM_017015136.2:c.3367G>A	XP_016870625.1:p.Val1123Ile
XM_017015137.1:c.3352G>A	XP_016870626.1:p.Val1118Ile
XM_017015138.1:c.3352G>A	XP_016870627.1:p.Val1118Ile
XM_024447674.1:c.3295G>A	XP_024303442.1:p.Val1099Ile
XM_024447675.1:c.3229G>A	XP_024303443.1:p.Val1077Ile
XM_024447676.1:c.2590G>A	XP_024303444.1:p.Val864Ile
XM_024447677.1:c.2590G>A	XP_024303445.1:p.Val864Ile
XM_024447680.1:c.3208G>A	XP_024303448.1:p.Val1070Ile
NM_024757.5:c.3466G>A MANE Select	NP_079033.4:p.Val1156Ile
NM_001354263.2:c.3445G>A	NP_001341192.1:p.Val1149Ile