Canonical Allele Identifier: CA375773730

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140712565C>A (hg19) ; chr9:g.137818113C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137818113C>A , CM000671.2:g.137818113C>A	GRCh38
NC_000009.11:g.140712565C>A , CM000671.1:g.140712565C>A	GRCh37
NC_000009.10:g.139832386C>A	NCBI36
NG_011776.1:g.204122C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3515C>A MANE Select	ENSP00000417980.1:p.Ser1172Tyr
ENST00000636472.1:n.77C>A
ENST00000636526.1:n.1C>A
ENST00000637161.1:c.3422C>A	ENSP00000490328.1:p.Ser1141Tyr
ENST00000637261.1:c.4089C>A	ENSP00000490815.1:n.4089C>A
ENST00000637748.1:n.496C>A
ENST00000637891.1:c.1589C>A	ENSP00000490907.1:n.1589C>A
ENST00000460843.5:c.3515C>A	ENSP00000417980.1:p.Ser1172Tyr
ENST00000462942.3:c.2372C>A	ENSP00000436107.1:p.Ser791Tyr
ENST00000475564.5:n.1239C>A
ENST00000494249.5:n.868C>A
NM_024757.4:c.3515C>A	NP_079033.4:p.Ser1172Tyr
XM_005266105.3:c.3506C>A	XP_005266162.1:p.Ser1169Tyr
XM_005266110.1:c.3422C>A	XP_005266167.1:p.Ser1141Tyr
XM_006717288.2:c.3497C>A	XP_006717351.1:p.Ser1166Tyr
XM_011519021.1:c.3524C>A	XP_011517323.1:p.Ser1175Tyr
XM_011519022.1:c.3521C>A	XP_011517324.1:p.Ser1174Tyr
XM_011519023.1:c.3503C>A	XP_011517325.1:p.Ser1168Tyr
XM_011519024.1:c.3446C>A	XP_011517326.1:p.Ser1149Tyr
XM_011519025.1:c.3422C>A	XP_011517327.1:p.Ser1141Tyr
XM_011519026.1:c.3380C>A	XP_011517328.1:p.Ser1127Tyr
XM_011519029.1:c.1946C>A	XP_011517331.1:p.Ser649Tyr
XM_011519030.1:c.1298C>A	XP_011517332.1:p.Ser433Tyr
XM_011519031.1:c.1085C>A	XP_011517333.1:p.Ser362Tyr
XM_011519032.1:c.1085C>A	XP_011517334.1:p.Ser362Tyr
XM_011519033.1:c.3359C>A	XP_011517335.1:p.Ser1120Tyr
XR_930459.1:n.5297-3551G>T
NM_001354263.1:c.3494C>A	NP_001341192.1:p.Ser1165Tyr
XM_005266105.5:c.3506C>A	XP_005266162.1:p.Ser1169Tyr
XM_011519021.3:c.3524C>A	XP_011517323.1:p.Ser1175Tyr
XM_011519022.3:c.3521C>A	XP_011517324.1:p.Ser1174Tyr
XM_011519023.3:c.3503C>A	XP_011517325.1:p.Ser1168Tyr
XM_011519029.3:c.1946C>A	XP_011517331.1:p.Ser649Tyr
XM_011519030.3:c.1298C>A	XP_011517332.1:p.Ser433Tyr
XM_017015134.1:c.3500C>A	XP_016870623.1:p.Ser1167Tyr
XM_017015136.2:c.3416C>A	XP_016870625.1:p.Ser1139Tyr
XM_017015137.1:c.3401C>A	XP_016870626.1:p.Ser1134Tyr
XM_017015138.1:c.3401C>A	XP_016870627.1:p.Ser1134Tyr
XM_024447674.1:c.3344C>A	XP_024303442.1:p.Ser1115Tyr
XM_024447675.1:c.3278C>A	XP_024303443.1:p.Ser1093Tyr
XM_024447676.1:c.2639C>A	XP_024303444.1:p.Ser880Tyr
XM_024447677.1:c.2639C>A	XP_024303445.1:p.Ser880Tyr
XM_024447680.1:c.3257C>A	XP_024303448.1:p.Ser1086Tyr
NM_024757.5:c.3515C>A MANE Select	NP_079033.4:p.Ser1172Tyr
NM_001354263.2:c.3494C>A	NP_001341192.1:p.Ser1165Tyr