Canonical Allele Identifier: CA375789014

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695418C>G (hg19) ; chr9:g.137800966C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800966C>G , CM000671.2:g.137800966C>G	GRCh38
NC_000009.11:g.140695418C>G , CM000671.1:g.140695418C>G	GRCh37
NC_000009.10:g.139815239C>G	NCBI36
NG_011776.1:g.186975C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2694C>G MANE Select	ENSP00000417980.1:p.Asp898Glu
ENST00000636027.1:c.2580C>G	ENSP00000489961.1:p.Asp860Glu
ENST00000637161.1:c.2601C>G	ENSP00000490328.1:p.Asp867Glu
ENST00000637261.1:c.2734C>G	ENSP00000490815.1:n.2734C>G
ENST00000637891.1:c.588C>G	ENSP00000490907.1:p.Asp196Glu
ENST00000637949.1:c.372C>G	ENSP00000489786.1:p.Asp124Glu
ENST00000460843.5:c.2694C>G	ENSP00000417980.1:p.Asp898Glu
ENST00000462942.3:c.1551C>G	ENSP00000436107.1:p.Asp517Glu
ENST00000482340.5:c.264C>G	ENSP00000486748.1:p.Asp88Glu
ENST00000486164.5:c.272C>G
ENST00000488242.2:n.220C>G
ENST00000493484.5:c.264C>G	ENSP00000486503.1:p.Asp88Glu
NM_024757.4:c.2694C>G	NP_079033.4:p.Asp898Glu
XM_005266105.3:c.2685C>G	XP_005266162.1:p.Asp895Glu
XM_005266110.1:c.2601C>G	XP_005266167.1:p.Asp867Glu
XM_006717288.2:c.2676C>G	XP_006717351.1:p.Asp892Glu
XM_011519021.1:c.2703C>G	XP_011517323.1:p.Asp901Glu
XM_011519022.1:c.2700C>G	XP_011517324.1:p.Asp900Glu
XM_011519023.1:c.2682C>G	XP_011517325.1:p.Asp894Glu
XM_011519024.1:c.2625C>G	XP_011517326.1:p.Asp875Glu
XM_011519025.1:c.2601C>G	XP_011517327.1:p.Asp867Glu
XM_011519026.1:c.2559C>G	XP_011517328.1:p.Asp853Glu
XM_011519027.1:c.2703C>G	XP_011517329.1:p.Asp901Glu
XM_011519029.1:c.1125C>G	XP_011517331.1:p.Asp375Glu
XM_011519030.1:c.477C>G	XP_011517332.1:p.Asp159Glu
XM_011519031.1:c.264C>G	XP_011517333.1:p.Asp88Glu
XM_011519032.1:c.264C>G	XP_011517334.1:p.Asp88Glu
XM_011519033.1:c.2538C>G	XP_011517335.1:p.Asp846Glu
NM_001354263.1:c.2673C>G	NP_001341192.1:p.Asp891Glu
XM_005266105.5:c.2685C>G	XP_005266162.1:p.Asp895Glu
XM_011519021.3:c.2703C>G	XP_011517323.1:p.Asp901Glu
XM_011519022.3:c.2700C>G	XP_011517324.1:p.Asp900Glu
XM_011519023.3:c.2682C>G	XP_011517325.1:p.Asp894Glu
XM_011519029.3:c.1125C>G	XP_011517331.1:p.Asp375Glu
XM_011519030.3:c.477C>G	XP_011517332.1:p.Asp159Glu
XM_017015134.1:c.2679C>G	XP_016870623.1:p.Asp893Glu
XM_017015136.2:c.2595C>G	XP_016870625.1:p.Asp865Glu
XM_017015137.1:c.2580C>G	XP_016870626.1:p.Asp860Glu
XM_017015138.1:c.2580C>G	XP_016870627.1:p.Asp860Glu
XM_024447674.1:c.2523C>G	XP_024303442.1:p.Asp841Glu
XM_024447675.1:c.2457C>G	XP_024303443.1:p.Asp819Glu
XM_024447676.1:c.1818C>G	XP_024303444.1:p.Asp606Glu
XM_024447677.1:c.1818C>G	XP_024303445.1:p.Asp606Glu
XM_024447678.1:c.2601C>G	XP_024303446.1:p.Asp867Glu
XM_024447680.1:c.2436C>G	XP_024303448.1:p.Asp812Glu
NM_024757.5:c.2694C>G MANE Select	NP_079033.4:p.Asp898Glu
NM_001354263.2:c.2673C>G	NP_001341192.1:p.Asp891Glu