Canonical Allele Identifier: CA468161036

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707488C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813036C>G , CM000671.2:g.137813036C>G	GRCh38
NC_000009.11:g.140707488C>G , CM000671.1:g.140707488C>G	GRCh37
NC_000009.10:g.139827309C>G	NCBI36
NG_011776.1:g.199045C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2898C>G MANE Select	ENSP00000417980.1:p.Thr966=
ENST00000636027.1:c.2784C>G	ENSP00000489961.1:p.Thr928=
ENST00000637161.1:c.2805C>G	ENSP00000490328.1:p.Thr935=
ENST00000637261.1:c.2938C>G	ENSP00000490815.1:n.2938C>G
ENST00000637891.1:c.792C>G	ENSP00000490907.1:p.Thr264=
ENST00000460843.5:c.2898C>G	ENSP00000417980.1:p.Thr966=
ENST00000462942.3:c.1755C>G	ENSP00000436107.1:p.Thr585=
ENST00000486164.5:c.585C>G
ENST00000488242.2:n.424C>G
NM_024757.4:c.2898C>G	NP_079033.4:p.Thr966=
XM_005266105.3:c.2889C>G	XP_005266162.1:p.Thr963=
XM_005266110.1:c.2805C>G	XP_005266167.1:p.Thr935=
XM_006717288.2:c.2880C>G	XP_006717351.1:p.Thr960=
XM_011519021.1:c.2907C>G	XP_011517323.1:p.Thr969=
XM_011519022.1:c.2904C>G	XP_011517324.1:p.Thr968=
XM_011519023.1:c.2886C>G	XP_011517325.1:p.Thr962=
XM_011519024.1:c.2829C>G	XP_011517326.1:p.Thr943=
XM_011519025.1:c.2805C>G	XP_011517327.1:p.Thr935=
XM_011519026.1:c.2763C>G	XP_011517328.1:p.Thr921=
XM_011519029.1:c.1329C>G	XP_011517331.1:p.Thr443=
XM_011519030.1:c.681C>G	XP_011517332.1:p.Thr227=
XM_011519031.1:c.468C>G	XP_011517333.1:p.Thr156=
XM_011519032.1:c.468C>G	XP_011517334.1:p.Thr156=
XM_011519033.1:c.2742C>G	XP_011517335.1:p.Thr914=
NM_001354263.1:c.2877C>G	NP_001341192.1:p.Thr959=
XM_005266105.5:c.2889C>G	XP_005266162.1:p.Thr963=
XM_011519021.3:c.2907C>G	XP_011517323.1:p.Thr969=
XM_011519022.3:c.2904C>G	XP_011517324.1:p.Thr968=
XM_011519023.3:c.2886C>G	XP_011517325.1:p.Thr962=
XM_011519029.3:c.1329C>G	XP_011517331.1:p.Thr443=
XM_011519030.3:c.681C>G	XP_011517332.1:p.Thr227=
XM_017015134.1:c.2883C>G	XP_016870623.1:p.Thr961=
XM_017015136.2:c.2799C>G	XP_016870625.1:p.Thr933=
XM_017015137.1:c.2784C>G	XP_016870626.1:p.Thr928=
XM_017015138.1:c.2784C>G	XP_016870627.1:p.Thr928=
XM_024447674.1:c.2727C>G	XP_024303442.1:p.Thr909=
XM_024447675.1:c.2661C>G	XP_024303443.1:p.Thr887=
XM_024447676.1:c.2022C>G	XP_024303444.1:p.Thr674=
XM_024447677.1:c.2022C>G	XP_024303445.1:p.Thr674=
XM_024447680.1:c.2640C>G	XP_024303448.1:p.Thr880=
NM_024757.5:c.2898C>G MANE Select	NP_079033.4:p.Thr966=
NM_001354263.2:c.2877C>G	NP_001341192.1:p.Thr959=