Canonical Allele Identifier: CA375793687

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707597C>A (hg19) ; chr9:g.137813145C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813145C>A , CM000671.2:g.137813145C>A	GRCh38
NC_000009.11:g.140707597C>A , CM000671.1:g.140707597C>A	GRCh37
NC_000009.10:g.139827418C>A	NCBI36
NG_011776.1:g.199154C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3007C>A MANE Select	ENSP00000417980.1:p.Pro1003Thr
ENST00000636027.1:c.2893C>A	ENSP00000489961.1:p.Pro965Thr
ENST00000637161.1:c.2914C>A	ENSP00000490328.1:p.Pro972Thr
ENST00000637261.1:c.3047C>A	ENSP00000490815.1:n.3047C>A
ENST00000637891.1:c.901C>A	ENSP00000490907.1:p.Pro301Thr
ENST00000460843.5:c.3007C>A	ENSP00000417980.1:p.Pro1003Thr
ENST00000462942.3:c.1864C>A	ENSP00000436107.1:p.Pro622Thr
ENST00000486164.5:c.694C>A
ENST00000488242.2:n.533C>A
NM_024757.4:c.3007C>A	NP_079033.4:p.Pro1003Thr
XM_005266105.3:c.2998C>A	XP_005266162.1:p.Pro1000Thr
XM_005266110.1:c.2914C>A	XP_005266167.1:p.Pro972Thr
XM_006717288.2:c.2989C>A	XP_006717351.1:p.Pro997Thr
XM_011519021.1:c.3016C>A	XP_011517323.1:p.Pro1006Thr
XM_011519022.1:c.3013C>A	XP_011517324.1:p.Pro1005Thr
XM_011519023.1:c.2995C>A	XP_011517325.1:p.Pro999Thr
XM_011519024.1:c.2938C>A	XP_011517326.1:p.Pro980Thr
XM_011519025.1:c.2914C>A	XP_011517327.1:p.Pro972Thr
XM_011519026.1:c.2872C>A	XP_011517328.1:p.Pro958Thr
XM_011519029.1:c.1438C>A	XP_011517331.1:p.Pro480Thr
XM_011519030.1:c.790C>A	XP_011517332.1:p.Pro264Thr
XM_011519031.1:c.577C>A	XP_011517333.1:p.Pro193Thr
XM_011519032.1:c.577C>A	XP_011517334.1:p.Pro193Thr
XM_011519033.1:c.2851C>A	XP_011517335.1:p.Pro951Thr
NM_001354263.1:c.2986C>A	NP_001341192.1:p.Pro996Thr
XM_005266105.5:c.2998C>A	XP_005266162.1:p.Pro1000Thr
XM_011519021.3:c.3016C>A	XP_011517323.1:p.Pro1006Thr
XM_011519022.3:c.3013C>A	XP_011517324.1:p.Pro1005Thr
XM_011519023.3:c.2995C>A	XP_011517325.1:p.Pro999Thr
XM_011519029.3:c.1438C>A	XP_011517331.1:p.Pro480Thr
XM_011519030.3:c.790C>A	XP_011517332.1:p.Pro264Thr
XM_017015134.1:c.2992C>A	XP_016870623.1:p.Pro998Thr
XM_017015136.2:c.2908C>A	XP_016870625.1:p.Pro970Thr
XM_017015137.1:c.2893C>A	XP_016870626.1:p.Pro965Thr
XM_017015138.1:c.2893C>A	XP_016870627.1:p.Pro965Thr
XM_024447674.1:c.2836C>A	XP_024303442.1:p.Pro946Thr
XM_024447675.1:c.2770C>A	XP_024303443.1:p.Pro924Thr
XM_024447676.1:c.2131C>A	XP_024303444.1:p.Pro711Thr
XM_024447677.1:c.2131C>A	XP_024303445.1:p.Pro711Thr
XM_024447680.1:c.2749C>A	XP_024303448.1:p.Pro917Thr
NM_024757.5:c.3007C>A MANE Select	NP_079033.4:p.Pro1003Thr
NM_001354263.2:c.2986C>A	NP_001341192.1:p.Pro996Thr