Canonical Allele Identifier: CA468161089

Gene: EHMT1

Linked Data

• dbSNP Id: rs778296046
• MyVariant Identifiers: chr9:g.140707584G>T (hg19) ; chr9:g.137813132G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813132G>T , CM000671.2:g.137813132G>T	GRCh38
NC_000009.11:g.140707584G>T , CM000671.1:g.140707584G>T	GRCh37
NC_000009.10:g.139827405G>T	NCBI36
NG_011776.1:g.199141G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2994G>T MANE Select	ENSP00000417980.1:p.Ser998=
ENST00000636027.1:c.2880G>T	ENSP00000489961.1:p.Ser960=
ENST00000637161.1:c.2901G>T	ENSP00000490328.1:p.Ser967=
ENST00000637261.1:c.3034G>T	ENSP00000490815.1:n.3034G>T
ENST00000637891.1:c.888G>T	ENSP00000490907.1:p.Ser296=
ENST00000460843.5:c.2994G>T	ENSP00000417980.1:p.Ser998=
ENST00000462942.3:c.1851G>T	ENSP00000436107.1:p.Ser617=
ENST00000486164.5:c.681G>T
ENST00000488242.2:n.520G>T
NM_024757.4:c.2994G>T	NP_079033.4:p.Ser998=
XM_005266105.3:c.2985G>T	XP_005266162.1:p.Ser995=
XM_005266110.1:c.2901G>T	XP_005266167.1:p.Ser967=
XM_006717288.2:c.2976G>T	XP_006717351.1:p.Ser992=
XM_011519021.1:c.3003G>T	XP_011517323.1:p.Ser1001=
XM_011519022.1:c.3000G>T	XP_011517324.1:p.Ser1000=
XM_011519023.1:c.2982G>T	XP_011517325.1:p.Ser994=
XM_011519024.1:c.2925G>T	XP_011517326.1:p.Ser975=
XM_011519025.1:c.2901G>T	XP_011517327.1:p.Ser967=
XM_011519026.1:c.2859G>T	XP_011517328.1:p.Ser953=
XM_011519029.1:c.1425G>T	XP_011517331.1:p.Ser475=
XM_011519030.1:c.777G>T	XP_011517332.1:p.Ser259=
XM_011519031.1:c.564G>T	XP_011517333.1:p.Ser188=
XM_011519032.1:c.564G>T	XP_011517334.1:p.Ser188=
XM_011519033.1:c.2838G>T	XP_011517335.1:p.Ser946=
NM_001354263.1:c.2973G>T	NP_001341192.1:p.Ser991=
XM_005266105.5:c.2985G>T	XP_005266162.1:p.Ser995=
XM_011519021.3:c.3003G>T	XP_011517323.1:p.Ser1001=
XM_011519022.3:c.3000G>T	XP_011517324.1:p.Ser1000=
XM_011519023.3:c.2982G>T	XP_011517325.1:p.Ser994=
XM_011519029.3:c.1425G>T	XP_011517331.1:p.Ser475=
XM_011519030.3:c.777G>T	XP_011517332.1:p.Ser259=
XM_017015134.1:c.2979G>T	XP_016870623.1:p.Ser993=
XM_017015136.2:c.2895G>T	XP_016870625.1:p.Ser965=
XM_017015137.1:c.2880G>T	XP_016870626.1:p.Ser960=
XM_017015138.1:c.2880G>T	XP_016870627.1:p.Ser960=
XM_024447674.1:c.2823G>T	XP_024303442.1:p.Ser941=
XM_024447675.1:c.2757G>T	XP_024303443.1:p.Ser919=
XM_024447676.1:c.2118G>T	XP_024303444.1:p.Ser706=
XM_024447677.1:c.2118G>T	XP_024303445.1:p.Ser706=
XM_024447680.1:c.2736G>T	XP_024303448.1:p.Ser912=
NM_024757.5:c.2994G>T MANE Select	NP_079033.4:p.Ser998=
NM_001354263.2:c.2973G>T	NP_001341192.1:p.Ser991=