Canonical Allele Identifier: CA375788690

Gene: EHMT1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2609A>C MANE Select	ENSP00000417980.1:p.Asp870Ala
ENST00000636027.1:c.2495A>C	ENSP00000489961.1:p.Asp832Ala
ENST00000637161.1:c.2516A>C	ENSP00000490328.1:p.Asp839Ala
ENST00000637261.1:c.2649A>C	ENSP00000490815.1:n.2649A>C
ENST00000637891.1:c.503A>C	ENSP00000490907.1:p.Asp168Ala
ENST00000637949.1:c.287A>C	ENSP00000489786.1:p.Asp96Ala
ENST00000460843.5:c.2609A>C	ENSP00000417980.1:p.Asp870Ala
ENST00000462942.3:c.1466A>C	ENSP00000436107.1:p.Asp489Ala
ENST00000482340.5:c.179A>C	ENSP00000486748.1:p.Asp60Ala
ENST00000486164.5:c.187A>C
ENST00000488242.2:n.135A>C
ENST00000493484.5:c.179A>C	ENSP00000486503.1:p.Asp60Ala
NM_024757.4:c.2609A>C	NP_079033.4:p.Asp870Ala
XM_005266105.3:c.2600A>C	XP_005266162.1:p.Asp867Ala
XM_005266110.1:c.2516A>C	XP_005266167.1:p.Asp839Ala
XM_006717288.2:c.2591A>C	XP_006717351.1:p.Asp864Ala
XM_011519021.1:c.2618A>C	XP_011517323.1:p.Asp873Ala
XM_011519022.1:c.2615A>C	XP_011517324.1:p.Asp872Ala
XM_011519023.1:c.2597A>C	XP_011517325.1:p.Asp866Ala
XM_011519024.1:c.2540A>C	XP_011517326.1:p.Asp847Ala
XM_011519025.1:c.2516A>C	XP_011517327.1:p.Asp839Ala
XM_011519026.1:c.2474A>C	XP_011517328.1:p.Asp825Ala
XM_011519027.1:c.2618A>C	XP_011517329.1:p.Asp873Ala
XM_011519029.1:c.1040A>C	XP_011517331.1:p.Asp347Ala
XM_011519030.1:c.392A>C	XP_011517332.1:p.Asp131Ala
XM_011519031.1:c.179A>C	XP_011517333.1:p.Asp60Ala
XM_011519032.1:c.179A>C	XP_011517334.1:p.Asp60Ala
XM_011519033.1:c.2453A>C	XP_011517335.1:p.Asp818Ala
NM_001354263.1:c.2588A>C	NP_001341192.1:p.Asp863Ala
XM_005266105.5:c.2600A>C	XP_005266162.1:p.Asp867Ala
XM_011519021.3:c.2618A>C	XP_011517323.1:p.Asp873Ala
XM_011519022.3:c.2615A>C	XP_011517324.1:p.Asp872Ala
XM_011519023.3:c.2597A>C	XP_011517325.1:p.Asp866Ala
XM_011519029.3:c.1040A>C	XP_011517331.1:p.Asp347Ala
XM_011519030.3:c.392A>C	XP_011517332.1:p.Asp131Ala
XM_017015134.1:c.2594A>C	XP_016870623.1:p.Asp865Ala
XM_017015136.2:c.2510A>C	XP_016870625.1:p.Asp837Ala
XM_017015137.1:c.2495A>C	XP_016870626.1:p.Asp832Ala
XM_017015138.1:c.2495A>C	XP_016870627.1:p.Asp832Ala
XM_024447674.1:c.2438A>C	XP_024303442.1:p.Asp813Ala
XM_024447675.1:c.2372A>C	XP_024303443.1:p.Asp791Ala
XM_024447676.1:c.1733A>C	XP_024303444.1:p.Asp578Ala
XM_024447677.1:c.1733A>C	XP_024303445.1:p.Asp578Ala
XM_024447678.1:c.2516A>C	XP_024303446.1:p.Asp839Ala
XM_024447680.1:c.2351A>C	XP_024303448.1:p.Asp784Ala
NM_024757.5:c.2609A>C MANE Select	NP_079033.4:p.Asp870Ala
NM_001354263.2:c.2588A>C	NP_001341192.1:p.Asp863Ala