Canonical Allele Identifier: CA375793370

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707511C>G (hg19) ; chr9:g.137813059C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813059C>G , CM000671.2:g.137813059C>G	GRCh38
NC_000009.11:g.140707511C>G , CM000671.1:g.140707511C>G	GRCh37
NC_000009.10:g.139827332C>G	NCBI36
NG_011776.1:g.199068C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2921C>G MANE Select	ENSP00000417980.1:p.Thr974Arg
ENST00000636027.1:c.2807C>G	ENSP00000489961.1:p.Thr936Arg
ENST00000637161.1:c.2828C>G	ENSP00000490328.1:p.Thr943Arg
ENST00000637261.1:c.2961C>G	ENSP00000490815.1:n.2961C>G
ENST00000637891.1:c.815C>G	ENSP00000490907.1:p.Thr272Arg
ENST00000460843.5:c.2921C>G	ENSP00000417980.1:p.Thr974Arg
ENST00000462942.3:c.1778C>G	ENSP00000436107.1:p.Thr593Arg
ENST00000486164.5:c.608C>G
ENST00000488242.2:n.447C>G
NM_024757.4:c.2921C>G	NP_079033.4:p.Thr974Arg
XM_005266105.3:c.2912C>G	XP_005266162.1:p.Thr971Arg
XM_005266110.1:c.2828C>G	XP_005266167.1:p.Thr943Arg
XM_006717288.2:c.2903C>G	XP_006717351.1:p.Thr968Arg
XM_011519021.1:c.2930C>G	XP_011517323.1:p.Thr977Arg
XM_011519022.1:c.2927C>G	XP_011517324.1:p.Thr976Arg
XM_011519023.1:c.2909C>G	XP_011517325.1:p.Thr970Arg
XM_011519024.1:c.2852C>G	XP_011517326.1:p.Thr951Arg
XM_011519025.1:c.2828C>G	XP_011517327.1:p.Thr943Arg
XM_011519026.1:c.2786C>G	XP_011517328.1:p.Thr929Arg
XM_011519029.1:c.1352C>G	XP_011517331.1:p.Thr451Arg
XM_011519030.1:c.704C>G	XP_011517332.1:p.Thr235Arg
XM_011519031.1:c.491C>G	XP_011517333.1:p.Thr164Arg
XM_011519032.1:c.491C>G	XP_011517334.1:p.Thr164Arg
XM_011519033.1:c.2765C>G	XP_011517335.1:p.Thr922Arg
NM_001354263.1:c.2900C>G	NP_001341192.1:p.Thr967Arg
XM_005266105.5:c.2912C>G	XP_005266162.1:p.Thr971Arg
XM_011519021.3:c.2930C>G	XP_011517323.1:p.Thr977Arg
XM_011519022.3:c.2927C>G	XP_011517324.1:p.Thr976Arg
XM_011519023.3:c.2909C>G	XP_011517325.1:p.Thr970Arg
XM_011519029.3:c.1352C>G	XP_011517331.1:p.Thr451Arg
XM_011519030.3:c.704C>G	XP_011517332.1:p.Thr235Arg
XM_017015134.1:c.2906C>G	XP_016870623.1:p.Thr969Arg
XM_017015136.2:c.2822C>G	XP_016870625.1:p.Thr941Arg
XM_017015137.1:c.2807C>G	XP_016870626.1:p.Thr936Arg
XM_017015138.1:c.2807C>G	XP_016870627.1:p.Thr936Arg
XM_024447674.1:c.2750C>G	XP_024303442.1:p.Thr917Arg
XM_024447675.1:c.2684C>G	XP_024303443.1:p.Thr895Arg
XM_024447676.1:c.2045C>G	XP_024303444.1:p.Thr682Arg
XM_024447677.1:c.2045C>G	XP_024303445.1:p.Thr682Arg
XM_024447680.1:c.2663C>G	XP_024303448.1:p.Thr888Arg
NM_024757.5:c.2921C>G MANE Select	NP_079033.4:p.Thr974Arg
NM_001354263.2:c.2900C>G	NP_001341192.1:p.Thr967Arg