Canonical Allele Identifier: CA375788761

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695351C>T (hg19) ; chr9:g.137800899C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800899C>T , CM000671.2:g.137800899C>T	GRCh38
NC_000009.11:g.140695351C>T , CM000671.1:g.140695351C>T	GRCh37
NC_000009.10:g.139815172C>T	NCBI36
NG_011776.1:g.186908C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2627C>T MANE Select	ENSP00000417980.1:p.Pro876Leu
ENST00000636027.1:c.2513C>T	ENSP00000489961.1:p.Pro838Leu
ENST00000637161.1:c.2534C>T	ENSP00000490328.1:p.Pro845Leu
ENST00000637261.1:c.2667C>T	ENSP00000490815.1:n.2667C>T
ENST00000637891.1:c.521C>T	ENSP00000490907.1:p.Pro174Leu
ENST00000637949.1:c.305C>T	ENSP00000489786.1:p.Pro102Leu
ENST00000460843.5:c.2627C>T	ENSP00000417980.1:p.Pro876Leu
ENST00000462942.3:c.1484C>T	ENSP00000436107.1:p.Pro495Leu
ENST00000482340.5:c.197C>T	ENSP00000486748.1:p.Pro66Leu
ENST00000486164.5:c.205C>T
ENST00000488242.2:n.153C>T
ENST00000493484.5:c.197C>T	ENSP00000486503.1:p.Pro66Leu
NM_024757.4:c.2627C>T	NP_079033.4:p.Pro876Leu
XM_005266105.3:c.2618C>T	XP_005266162.1:p.Pro873Leu
XM_005266110.1:c.2534C>T	XP_005266167.1:p.Pro845Leu
XM_006717288.2:c.2609C>T	XP_006717351.1:p.Pro870Leu
XM_011519021.1:c.2636C>T	XP_011517323.1:p.Pro879Leu
XM_011519022.1:c.2633C>T	XP_011517324.1:p.Pro878Leu
XM_011519023.1:c.2615C>T	XP_011517325.1:p.Pro872Leu
XM_011519024.1:c.2558C>T	XP_011517326.1:p.Pro853Leu
XM_011519025.1:c.2534C>T	XP_011517327.1:p.Pro845Leu
XM_011519026.1:c.2492C>T	XP_011517328.1:p.Pro831Leu
XM_011519027.1:c.2636C>T	XP_011517329.1:p.Pro879Leu
XM_011519029.1:c.1058C>T	XP_011517331.1:p.Pro353Leu
XM_011519030.1:c.410C>T	XP_011517332.1:p.Pro137Leu
XM_011519031.1:c.197C>T	XP_011517333.1:p.Pro66Leu
XM_011519032.1:c.197C>T	XP_011517334.1:p.Pro66Leu
XM_011519033.1:c.2471C>T	XP_011517335.1:p.Pro824Leu
NM_001354263.1:c.2606C>T	NP_001341192.1:p.Pro869Leu
XM_005266105.5:c.2618C>T	XP_005266162.1:p.Pro873Leu
XM_011519021.3:c.2636C>T	XP_011517323.1:p.Pro879Leu
XM_011519022.3:c.2633C>T	XP_011517324.1:p.Pro878Leu
XM_011519023.3:c.2615C>T	XP_011517325.1:p.Pro872Leu
XM_011519029.3:c.1058C>T	XP_011517331.1:p.Pro353Leu
XM_011519030.3:c.410C>T	XP_011517332.1:p.Pro137Leu
XM_017015134.1:c.2612C>T	XP_016870623.1:p.Pro871Leu
XM_017015136.2:c.2528C>T	XP_016870625.1:p.Pro843Leu
XM_017015137.1:c.2513C>T	XP_016870626.1:p.Pro838Leu
XM_017015138.1:c.2513C>T	XP_016870627.1:p.Pro838Leu
XM_024447674.1:c.2456C>T	XP_024303442.1:p.Pro819Leu
XM_024447675.1:c.2390C>T	XP_024303443.1:p.Pro797Leu
XM_024447676.1:c.1751C>T	XP_024303444.1:p.Pro584Leu
XM_024447677.1:c.1751C>T	XP_024303445.1:p.Pro584Leu
XM_024447678.1:c.2534C>T	XP_024303446.1:p.Pro845Leu
XM_024447680.1:c.2369C>T	XP_024303448.1:p.Pro790Leu
NM_024757.5:c.2627C>T MANE Select	NP_079033.4:p.Pro876Leu
NM_001354263.2:c.2606C>T	NP_001341192.1:p.Pro869Leu