Canonical Allele Identifier: CA375788828

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695368G>T (hg19) ; chr9:g.137800916G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800916G>T , CM000671.2:g.137800916G>T	GRCh38
NC_000009.11:g.140695368G>T , CM000671.1:g.140695368G>T	GRCh37
NC_000009.10:g.139815189G>T	NCBI36
NG_011776.1:g.186925G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2644G>T MANE Select	ENSP00000417980.1:p.Glu882Ter
ENST00000636027.1:c.2530G>T	ENSP00000489961.1:p.Glu844Ter
ENST00000637161.1:c.2551G>T	ENSP00000490328.1:p.Glu851Ter
ENST00000637261.1:c.2684G>T	ENSP00000490815.1:n.2684G>T
ENST00000637891.1:c.538G>T	ENSP00000490907.1:p.Glu180Ter
ENST00000637949.1:c.322G>T	ENSP00000489786.1:p.Glu108Ter
ENST00000460843.5:c.2644G>T	ENSP00000417980.1:p.Glu882Ter
ENST00000462942.3:c.1501G>T	ENSP00000436107.1:p.Glu501Ter
ENST00000482340.5:c.214G>T	ENSP00000486748.1:p.Glu72Ter
ENST00000486164.5:c.222G>T
ENST00000488242.2:n.170G>T
ENST00000493484.5:c.214G>T	ENSP00000486503.1:p.Glu72Ter
NM_024757.4:c.2644G>T	NP_079033.4:p.Glu882Ter
XM_005266105.3:c.2635G>T	XP_005266162.1:p.Glu879Ter
XM_005266110.1:c.2551G>T	XP_005266167.1:p.Glu851Ter
XM_006717288.2:c.2626G>T	XP_006717351.1:p.Glu876Ter
XM_011519021.1:c.2653G>T	XP_011517323.1:p.Glu885Ter
XM_011519022.1:c.2650G>T	XP_011517324.1:p.Glu884Ter
XM_011519023.1:c.2632G>T	XP_011517325.1:p.Glu878Ter
XM_011519024.1:c.2575G>T	XP_011517326.1:p.Glu859Ter
XM_011519025.1:c.2551G>T	XP_011517327.1:p.Glu851Ter
XM_011519026.1:c.2509G>T	XP_011517328.1:p.Glu837Ter
XM_011519027.1:c.2653G>T	XP_011517329.1:p.Glu885Ter
XM_011519029.1:c.1075G>T	XP_011517331.1:p.Glu359Ter
XM_011519030.1:c.427G>T	XP_011517332.1:p.Glu143Ter
XM_011519031.1:c.214G>T	XP_011517333.1:p.Glu72Ter
XM_011519032.1:c.214G>T	XP_011517334.1:p.Glu72Ter
XM_011519033.1:c.2488G>T	XP_011517335.1:p.Glu830Ter
NM_001354263.1:c.2623G>T	NP_001341192.1:p.Glu875Ter
XM_005266105.5:c.2635G>T	XP_005266162.1:p.Glu879Ter
XM_011519021.3:c.2653G>T	XP_011517323.1:p.Glu885Ter
XM_011519022.3:c.2650G>T	XP_011517324.1:p.Glu884Ter
XM_011519023.3:c.2632G>T	XP_011517325.1:p.Glu878Ter
XM_011519029.3:c.1075G>T	XP_011517331.1:p.Glu359Ter
XM_011519030.3:c.427G>T	XP_011517332.1:p.Glu143Ter
XM_017015134.1:c.2629G>T	XP_016870623.1:p.Glu877Ter
XM_017015136.2:c.2545G>T	XP_016870625.1:p.Glu849Ter
XM_017015137.1:c.2530G>T	XP_016870626.1:p.Glu844Ter
XM_017015138.1:c.2530G>T	XP_016870627.1:p.Glu844Ter
XM_024447674.1:c.2473G>T	XP_024303442.1:p.Glu825Ter
XM_024447675.1:c.2407G>T	XP_024303443.1:p.Glu803Ter
XM_024447676.1:c.1768G>T	XP_024303444.1:p.Glu590Ter
XM_024447677.1:c.1768G>T	XP_024303445.1:p.Glu590Ter
XM_024447678.1:c.2551G>T	XP_024303446.1:p.Glu851Ter
XM_024447680.1:c.2386G>T	XP_024303448.1:p.Glu796Ter
NM_024757.5:c.2644G>T MANE Select	NP_079033.4:p.Glu882Ter
NM_001354263.2:c.2623G>T	NP_001341192.1:p.Glu875Ter