Canonical Allele Identifier: CA375788876

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695378A>T (hg19) ; chr9:g.137800926A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800926A>T , CM000671.2:g.137800926A>T	GRCh38
NC_000009.11:g.140695378A>T , CM000671.1:g.140695378A>T	GRCh37
NC_000009.10:g.139815199A>T	NCBI36
NG_011776.1:g.186935A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2654A>T MANE Select	ENSP00000417980.1:p.His885Leu
ENST00000636027.1:c.2540A>T	ENSP00000489961.1:p.His847Leu
ENST00000637161.1:c.2561A>T	ENSP00000490328.1:p.His854Leu
ENST00000637261.1:c.2694A>T	ENSP00000490815.1:n.2694A>T
ENST00000637891.1:c.548A>T	ENSP00000490907.1:p.His183Leu
ENST00000637949.1:c.332A>T	ENSP00000489786.1:p.His111Leu
ENST00000460843.5:c.2654A>T	ENSP00000417980.1:p.His885Leu
ENST00000462942.3:c.1511A>T	ENSP00000436107.1:p.His504Leu
ENST00000482340.5:c.224A>T	ENSP00000486748.1:p.His75Leu
ENST00000486164.5:c.232A>T
ENST00000488242.2:n.180A>T
ENST00000493484.5:c.224A>T	ENSP00000486503.1:p.His75Leu
NM_024757.4:c.2654A>T	NP_079033.4:p.His885Leu
XM_005266105.3:c.2645A>T	XP_005266162.1:p.His882Leu
XM_005266110.1:c.2561A>T	XP_005266167.1:p.His854Leu
XM_006717288.2:c.2636A>T	XP_006717351.1:p.His879Leu
XM_011519021.1:c.2663A>T	XP_011517323.1:p.His888Leu
XM_011519022.1:c.2660A>T	XP_011517324.1:p.His887Leu
XM_011519023.1:c.2642A>T	XP_011517325.1:p.His881Leu
XM_011519024.1:c.2585A>T	XP_011517326.1:p.His862Leu
XM_011519025.1:c.2561A>T	XP_011517327.1:p.His854Leu
XM_011519026.1:c.2519A>T	XP_011517328.1:p.His840Leu
XM_011519027.1:c.2663A>T	XP_011517329.1:p.His888Leu
XM_011519029.1:c.1085A>T	XP_011517331.1:p.His362Leu
XM_011519030.1:c.437A>T	XP_011517332.1:p.His146Leu
XM_011519031.1:c.224A>T	XP_011517333.1:p.His75Leu
XM_011519032.1:c.224A>T	XP_011517334.1:p.His75Leu
XM_011519033.1:c.2498A>T	XP_011517335.1:p.His833Leu
NM_001354263.1:c.2633A>T	NP_001341192.1:p.His878Leu
XM_005266105.5:c.2645A>T	XP_005266162.1:p.His882Leu
XM_011519021.3:c.2663A>T	XP_011517323.1:p.His888Leu
XM_011519022.3:c.2660A>T	XP_011517324.1:p.His887Leu
XM_011519023.3:c.2642A>T	XP_011517325.1:p.His881Leu
XM_011519029.3:c.1085A>T	XP_011517331.1:p.His362Leu
XM_011519030.3:c.437A>T	XP_011517332.1:p.His146Leu
XM_017015134.1:c.2639A>T	XP_016870623.1:p.His880Leu
XM_017015136.2:c.2555A>T	XP_016870625.1:p.His852Leu
XM_017015137.1:c.2540A>T	XP_016870626.1:p.His847Leu
XM_017015138.1:c.2540A>T	XP_016870627.1:p.His847Leu
XM_024447674.1:c.2483A>T	XP_024303442.1:p.His828Leu
XM_024447675.1:c.2417A>T	XP_024303443.1:p.His806Leu
XM_024447676.1:c.1778A>T	XP_024303444.1:p.His593Leu
XM_024447677.1:c.1778A>T	XP_024303445.1:p.His593Leu
XM_024447678.1:c.2561A>T	XP_024303446.1:p.His854Leu
XM_024447680.1:c.2396A>T	XP_024303448.1:p.His799Leu
NM_024757.5:c.2654A>T MANE Select	NP_079033.4:p.His885Leu
NM_001354263.2:c.2633A>T	NP_001341192.1:p.His878Leu