Canonical Allele Identifier: CA375788758

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695350C>G (hg19) ; chr9:g.137800898C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800898C>G , CM000671.2:g.137800898C>G	GRCh38
NC_000009.11:g.140695350C>G , CM000671.1:g.140695350C>G	GRCh37
NC_000009.10:g.139815171C>G	NCBI36
NG_011776.1:g.186907C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2626C>G MANE Select	ENSP00000417980.1:p.Pro876Ala
ENST00000636027.1:c.2512C>G	ENSP00000489961.1:p.Pro838Ala
ENST00000637161.1:c.2533C>G	ENSP00000490328.1:p.Pro845Ala
ENST00000637261.1:c.2666C>G	ENSP00000490815.1:n.2666C>G
ENST00000637891.1:c.520C>G	ENSP00000490907.1:p.Pro174Ala
ENST00000637949.1:c.304C>G	ENSP00000489786.1:p.Pro102Ala
ENST00000460843.5:c.2626C>G	ENSP00000417980.1:p.Pro876Ala
ENST00000462942.3:c.1483C>G	ENSP00000436107.1:p.Pro495Ala
ENST00000482340.5:c.196C>G	ENSP00000486748.1:p.Pro66Ala
ENST00000486164.5:c.204C>G
ENST00000488242.2:n.152C>G
ENST00000493484.5:c.196C>G	ENSP00000486503.1:p.Pro66Ala
NM_024757.4:c.2626C>G	NP_079033.4:p.Pro876Ala
XM_005266105.3:c.2617C>G	XP_005266162.1:p.Pro873Ala
XM_005266110.1:c.2533C>G	XP_005266167.1:p.Pro845Ala
XM_006717288.2:c.2608C>G	XP_006717351.1:p.Pro870Ala
XM_011519021.1:c.2635C>G	XP_011517323.1:p.Pro879Ala
XM_011519022.1:c.2632C>G	XP_011517324.1:p.Pro878Ala
XM_011519023.1:c.2614C>G	XP_011517325.1:p.Pro872Ala
XM_011519024.1:c.2557C>G	XP_011517326.1:p.Pro853Ala
XM_011519025.1:c.2533C>G	XP_011517327.1:p.Pro845Ala
XM_011519026.1:c.2491C>G	XP_011517328.1:p.Pro831Ala
XM_011519027.1:c.2635C>G	XP_011517329.1:p.Pro879Ala
XM_011519029.1:c.1057C>G	XP_011517331.1:p.Pro353Ala
XM_011519030.1:c.409C>G	XP_011517332.1:p.Pro137Ala
XM_011519031.1:c.196C>G	XP_011517333.1:p.Pro66Ala
XM_011519032.1:c.196C>G	XP_011517334.1:p.Pro66Ala
XM_011519033.1:c.2470C>G	XP_011517335.1:p.Pro824Ala
NM_001354263.1:c.2605C>G	NP_001341192.1:p.Pro869Ala
XM_005266105.5:c.2617C>G	XP_005266162.1:p.Pro873Ala
XM_011519021.3:c.2635C>G	XP_011517323.1:p.Pro879Ala
XM_011519022.3:c.2632C>G	XP_011517324.1:p.Pro878Ala
XM_011519023.3:c.2614C>G	XP_011517325.1:p.Pro872Ala
XM_011519029.3:c.1057C>G	XP_011517331.1:p.Pro353Ala
XM_011519030.3:c.409C>G	XP_011517332.1:p.Pro137Ala
XM_017015134.1:c.2611C>G	XP_016870623.1:p.Pro871Ala
XM_017015136.2:c.2527C>G	XP_016870625.1:p.Pro843Ala
XM_017015137.1:c.2512C>G	XP_016870626.1:p.Pro838Ala
XM_017015138.1:c.2512C>G	XP_016870627.1:p.Pro838Ala
XM_024447674.1:c.2455C>G	XP_024303442.1:p.Pro819Ala
XM_024447675.1:c.2389C>G	XP_024303443.1:p.Pro797Ala
XM_024447676.1:c.1750C>G	XP_024303444.1:p.Pro584Ala
XM_024447677.1:c.1750C>G	XP_024303445.1:p.Pro584Ala
XM_024447678.1:c.2533C>G	XP_024303446.1:p.Pro845Ala
XM_024447680.1:c.2368C>G	XP_024303448.1:p.Pro790Ala
NM_024757.5:c.2626C>G MANE Select	NP_079033.4:p.Pro876Ala
NM_001354263.2:c.2605C>G	NP_001341192.1:p.Pro869Ala