Canonical Allele Identifier: CA375788931

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695393A>C (hg19) ; chr9:g.137800941A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800941A>C , CM000671.2:g.137800941A>C	GRCh38
NC_000009.11:g.140695393A>C , CM000671.1:g.140695393A>C	GRCh37
NC_000009.10:g.139815214A>C	NCBI36
NG_011776.1:g.186950A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2669A>C MANE Select	ENSP00000417980.1:p.Lys890Thr
ENST00000636027.1:c.2555A>C	ENSP00000489961.1:p.Lys852Thr
ENST00000637161.1:c.2576A>C	ENSP00000490328.1:p.Lys859Thr
ENST00000637261.1:c.2709A>C	ENSP00000490815.1:n.2709A>C
ENST00000637891.1:c.563A>C	ENSP00000490907.1:p.Lys188Thr
ENST00000637949.1:c.347A>C	ENSP00000489786.1:p.Lys116Thr
ENST00000460843.5:c.2669A>C	ENSP00000417980.1:p.Lys890Thr
ENST00000462942.3:c.1526A>C	ENSP00000436107.1:p.Lys509Thr
ENST00000482340.5:c.239A>C	ENSP00000486748.1:p.Lys80Thr
ENST00000486164.5:c.247A>C
ENST00000488242.2:n.195A>C
ENST00000493484.5:c.239A>C	ENSP00000486503.1:p.Lys80Thr
NM_024757.4:c.2669A>C	NP_079033.4:p.Lys890Thr
XM_005266105.3:c.2660A>C	XP_005266162.1:p.Lys887Thr
XM_005266110.1:c.2576A>C	XP_005266167.1:p.Lys859Thr
XM_006717288.2:c.2651A>C	XP_006717351.1:p.Lys884Thr
XM_011519021.1:c.2678A>C	XP_011517323.1:p.Lys893Thr
XM_011519022.1:c.2675A>C	XP_011517324.1:p.Lys892Thr
XM_011519023.1:c.2657A>C	XP_011517325.1:p.Lys886Thr
XM_011519024.1:c.2600A>C	XP_011517326.1:p.Lys867Thr
XM_011519025.1:c.2576A>C	XP_011517327.1:p.Lys859Thr
XM_011519026.1:c.2534A>C	XP_011517328.1:p.Lys845Thr
XM_011519027.1:c.2678A>C	XP_011517329.1:p.Lys893Thr
XM_011519029.1:c.1100A>C	XP_011517331.1:p.Lys367Thr
XM_011519030.1:c.452A>C	XP_011517332.1:p.Lys151Thr
XM_011519031.1:c.239A>C	XP_011517333.1:p.Lys80Thr
XM_011519032.1:c.239A>C	XP_011517334.1:p.Lys80Thr
XM_011519033.1:c.2513A>C	XP_011517335.1:p.Lys838Thr
NM_001354263.1:c.2648A>C	NP_001341192.1:p.Lys883Thr
XM_005266105.5:c.2660A>C	XP_005266162.1:p.Lys887Thr
XM_011519021.3:c.2678A>C	XP_011517323.1:p.Lys893Thr
XM_011519022.3:c.2675A>C	XP_011517324.1:p.Lys892Thr
XM_011519023.3:c.2657A>C	XP_011517325.1:p.Lys886Thr
XM_011519029.3:c.1100A>C	XP_011517331.1:p.Lys367Thr
XM_011519030.3:c.452A>C	XP_011517332.1:p.Lys151Thr
XM_017015134.1:c.2654A>C	XP_016870623.1:p.Lys885Thr
XM_017015136.2:c.2570A>C	XP_016870625.1:p.Lys857Thr
XM_017015137.1:c.2555A>C	XP_016870626.1:p.Lys852Thr
XM_017015138.1:c.2555A>C	XP_016870627.1:p.Lys852Thr
XM_024447674.1:c.2498A>C	XP_024303442.1:p.Lys833Thr
XM_024447675.1:c.2432A>C	XP_024303443.1:p.Lys811Thr
XM_024447676.1:c.1793A>C	XP_024303444.1:p.Lys598Thr
XM_024447677.1:c.1793A>C	XP_024303445.1:p.Lys598Thr
XM_024447678.1:c.2576A>C	XP_024303446.1:p.Lys859Thr
XM_024447680.1:c.2411A>C	XP_024303448.1:p.Lys804Thr
NM_024757.5:c.2669A>C MANE Select	NP_079033.4:p.Lys890Thr
NM_001354263.2:c.2648A>C	NP_001341192.1:p.Lys883Thr