Canonical Allele Identifier: CA375788692

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695333A>G (hg19) ; chr9:g.137800881A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800881A>G , CM000671.2:g.137800881A>G	GRCh38
NC_000009.11:g.140695333A>G , CM000671.1:g.140695333A>G	GRCh37
NC_000009.10:g.139815154A>G	NCBI36
NG_011776.1:g.186890A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2609A>G MANE Select	ENSP00000417980.1:p.Asp870Gly
ENST00000636027.1:c.2495A>G	ENSP00000489961.1:p.Asp832Gly
ENST00000637161.1:c.2516A>G	ENSP00000490328.1:p.Asp839Gly
ENST00000637261.1:c.2649A>G	ENSP00000490815.1:n.2649A>G
ENST00000637891.1:c.503A>G	ENSP00000490907.1:p.Asp168Gly
ENST00000637949.1:c.287A>G	ENSP00000489786.1:p.Asp96Gly
ENST00000460843.5:c.2609A>G	ENSP00000417980.1:p.Asp870Gly
ENST00000462942.3:c.1466A>G	ENSP00000436107.1:p.Asp489Gly
ENST00000482340.5:c.179A>G	ENSP00000486748.1:p.Asp60Gly
ENST00000486164.5:c.187A>G
ENST00000488242.2:n.135A>G
ENST00000493484.5:c.179A>G	ENSP00000486503.1:p.Asp60Gly
NM_024757.4:c.2609A>G	NP_079033.4:p.Asp870Gly
XM_005266105.3:c.2600A>G	XP_005266162.1:p.Asp867Gly
XM_005266110.1:c.2516A>G	XP_005266167.1:p.Asp839Gly
XM_006717288.2:c.2591A>G	XP_006717351.1:p.Asp864Gly
XM_011519021.1:c.2618A>G	XP_011517323.1:p.Asp873Gly
XM_011519022.1:c.2615A>G	XP_011517324.1:p.Asp872Gly
XM_011519023.1:c.2597A>G	XP_011517325.1:p.Asp866Gly
XM_011519024.1:c.2540A>G	XP_011517326.1:p.Asp847Gly
XM_011519025.1:c.2516A>G	XP_011517327.1:p.Asp839Gly
XM_011519026.1:c.2474A>G	XP_011517328.1:p.Asp825Gly
XM_011519027.1:c.2618A>G	XP_011517329.1:p.Asp873Gly
XM_011519029.1:c.1040A>G	XP_011517331.1:p.Asp347Gly
XM_011519030.1:c.392A>G	XP_011517332.1:p.Asp131Gly
XM_011519031.1:c.179A>G	XP_011517333.1:p.Asp60Gly
XM_011519032.1:c.179A>G	XP_011517334.1:p.Asp60Gly
XM_011519033.1:c.2453A>G	XP_011517335.1:p.Asp818Gly
NM_001354263.1:c.2588A>G	NP_001341192.1:p.Asp863Gly
XM_005266105.5:c.2600A>G	XP_005266162.1:p.Asp867Gly
XM_011519021.3:c.2618A>G	XP_011517323.1:p.Asp873Gly
XM_011519022.3:c.2615A>G	XP_011517324.1:p.Asp872Gly
XM_011519023.3:c.2597A>G	XP_011517325.1:p.Asp866Gly
XM_011519029.3:c.1040A>G	XP_011517331.1:p.Asp347Gly
XM_011519030.3:c.392A>G	XP_011517332.1:p.Asp131Gly
XM_017015134.1:c.2594A>G	XP_016870623.1:p.Asp865Gly
XM_017015136.2:c.2510A>G	XP_016870625.1:p.Asp837Gly
XM_017015137.1:c.2495A>G	XP_016870626.1:p.Asp832Gly
XM_017015138.1:c.2495A>G	XP_016870627.1:p.Asp832Gly
XM_024447674.1:c.2438A>G	XP_024303442.1:p.Asp813Gly
XM_024447675.1:c.2372A>G	XP_024303443.1:p.Asp791Gly
XM_024447676.1:c.1733A>G	XP_024303444.1:p.Asp578Gly
XM_024447677.1:c.1733A>G	XP_024303445.1:p.Asp578Gly
XM_024447678.1:c.2516A>G	XP_024303446.1:p.Asp839Gly
XM_024447680.1:c.2351A>G	XP_024303448.1:p.Asp784Gly
NM_024757.5:c.2609A>G MANE Select	NP_079033.4:p.Asp870Gly
NM_001354263.2:c.2588A>G	NP_001341192.1:p.Asp863Gly