Canonical Allele Identifier: CA375788821

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695366C>A (hg19) ; chr9:g.137800914C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800914C>A , CM000671.2:g.137800914C>A	GRCh38
NC_000009.11:g.140695366C>A , CM000671.1:g.140695366C>A	GRCh37
NC_000009.10:g.139815187C>A	NCBI36
NG_011776.1:g.186923C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2642C>A MANE Select	ENSP00000417980.1:p.Thr881Lys
ENST00000636027.1:c.2528C>A	ENSP00000489961.1:p.Thr843Lys
ENST00000637161.1:c.2549C>A	ENSP00000490328.1:p.Thr850Lys
ENST00000637261.1:c.2682C>A	ENSP00000490815.1:n.2682C>A
ENST00000637891.1:c.536C>A	ENSP00000490907.1:p.Thr179Lys
ENST00000637949.1:c.320C>A	ENSP00000489786.1:p.Thr107Lys
ENST00000460843.5:c.2642C>A	ENSP00000417980.1:p.Thr881Lys
ENST00000462942.3:c.1499C>A	ENSP00000436107.1:p.Thr500Lys
ENST00000482340.5:c.212C>A	ENSP00000486748.1:p.Thr71Lys
ENST00000486164.5:c.220C>A
ENST00000488242.2:n.168C>A
ENST00000493484.5:c.212C>A	ENSP00000486503.1:p.Thr71Lys
NM_024757.4:c.2642C>A	NP_079033.4:p.Thr881Lys
XM_005266105.3:c.2633C>A	XP_005266162.1:p.Thr878Lys
XM_005266110.1:c.2549C>A	XP_005266167.1:p.Thr850Lys
XM_006717288.2:c.2624C>A	XP_006717351.1:p.Thr875Lys
XM_011519021.1:c.2651C>A	XP_011517323.1:p.Thr884Lys
XM_011519022.1:c.2648C>A	XP_011517324.1:p.Thr883Lys
XM_011519023.1:c.2630C>A	XP_011517325.1:p.Thr877Lys
XM_011519024.1:c.2573C>A	XP_011517326.1:p.Thr858Lys
XM_011519025.1:c.2549C>A	XP_011517327.1:p.Thr850Lys
XM_011519026.1:c.2507C>A	XP_011517328.1:p.Thr836Lys
XM_011519027.1:c.2651C>A	XP_011517329.1:p.Thr884Lys
XM_011519029.1:c.1073C>A	XP_011517331.1:p.Thr358Lys
XM_011519030.1:c.425C>A	XP_011517332.1:p.Thr142Lys
XM_011519031.1:c.212C>A	XP_011517333.1:p.Thr71Lys
XM_011519032.1:c.212C>A	XP_011517334.1:p.Thr71Lys
XM_011519033.1:c.2486C>A	XP_011517335.1:p.Thr829Lys
NM_001354263.1:c.2621C>A	NP_001341192.1:p.Thr874Lys
XM_005266105.5:c.2633C>A	XP_005266162.1:p.Thr878Lys
XM_011519021.3:c.2651C>A	XP_011517323.1:p.Thr884Lys
XM_011519022.3:c.2648C>A	XP_011517324.1:p.Thr883Lys
XM_011519023.3:c.2630C>A	XP_011517325.1:p.Thr877Lys
XM_011519029.3:c.1073C>A	XP_011517331.1:p.Thr358Lys
XM_011519030.3:c.425C>A	XP_011517332.1:p.Thr142Lys
XM_017015134.1:c.2627C>A	XP_016870623.1:p.Thr876Lys
XM_017015136.2:c.2543C>A	XP_016870625.1:p.Thr848Lys
XM_017015137.1:c.2528C>A	XP_016870626.1:p.Thr843Lys
XM_017015138.1:c.2528C>A	XP_016870627.1:p.Thr843Lys
XM_024447674.1:c.2471C>A	XP_024303442.1:p.Thr824Lys
XM_024447675.1:c.2405C>A	XP_024303443.1:p.Thr802Lys
XM_024447676.1:c.1766C>A	XP_024303444.1:p.Thr589Lys
XM_024447677.1:c.1766C>A	XP_024303445.1:p.Thr589Lys
XM_024447678.1:c.2549C>A	XP_024303446.1:p.Thr850Lys
XM_024447680.1:c.2384C>A	XP_024303448.1:p.Thr795Lys
NM_024757.5:c.2642C>A MANE Select	NP_079033.4:p.Thr881Lys
NM_001354263.2:c.2621C>A	NP_001341192.1:p.Thr874Lys