Canonical Allele Identifier: CA375793361

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707508A>C (hg19) ; chr9:g.137813056A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813056A>C , CM000671.2:g.137813056A>C	GRCh38
NC_000009.11:g.140707508A>C , CM000671.1:g.140707508A>C	GRCh37
NC_000009.10:g.139827329A>C	NCBI36
NG_011776.1:g.199065A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2918A>C MANE Select	ENSP00000417980.1:p.Glu973Ala
ENST00000636027.1:c.2804A>C	ENSP00000489961.1:p.Glu935Ala
ENST00000637161.1:c.2825A>C	ENSP00000490328.1:p.Glu942Ala
ENST00000637261.1:c.2958A>C	ENSP00000490815.1:n.2958A>C
ENST00000637891.1:c.812A>C	ENSP00000490907.1:p.Glu271Ala
ENST00000460843.5:c.2918A>C	ENSP00000417980.1:p.Glu973Ala
ENST00000462942.3:c.1775A>C	ENSP00000436107.1:p.Glu592Ala
ENST00000486164.5:c.605A>C
ENST00000488242.2:n.444A>C
NM_024757.4:c.2918A>C	NP_079033.4:p.Glu973Ala
XM_005266105.3:c.2909A>C	XP_005266162.1:p.Glu970Ala
XM_005266110.1:c.2825A>C	XP_005266167.1:p.Glu942Ala
XM_006717288.2:c.2900A>C	XP_006717351.1:p.Glu967Ala
XM_011519021.1:c.2927A>C	XP_011517323.1:p.Glu976Ala
XM_011519022.1:c.2924A>C	XP_011517324.1:p.Glu975Ala
XM_011519023.1:c.2906A>C	XP_011517325.1:p.Glu969Ala
XM_011519024.1:c.2849A>C	XP_011517326.1:p.Glu950Ala
XM_011519025.1:c.2825A>C	XP_011517327.1:p.Glu942Ala
XM_011519026.1:c.2783A>C	XP_011517328.1:p.Glu928Ala
XM_011519029.1:c.1349A>C	XP_011517331.1:p.Glu450Ala
XM_011519030.1:c.701A>C	XP_011517332.1:p.Glu234Ala
XM_011519031.1:c.488A>C	XP_011517333.1:p.Glu163Ala
XM_011519032.1:c.488A>C	XP_011517334.1:p.Glu163Ala
XM_011519033.1:c.2762A>C	XP_011517335.1:p.Glu921Ala
NM_001354263.1:c.2897A>C	NP_001341192.1:p.Glu966Ala
XM_005266105.5:c.2909A>C	XP_005266162.1:p.Glu970Ala
XM_011519021.3:c.2927A>C	XP_011517323.1:p.Glu976Ala
XM_011519022.3:c.2924A>C	XP_011517324.1:p.Glu975Ala
XM_011519023.3:c.2906A>C	XP_011517325.1:p.Glu969Ala
XM_011519029.3:c.1349A>C	XP_011517331.1:p.Glu450Ala
XM_011519030.3:c.701A>C	XP_011517332.1:p.Glu234Ala
XM_017015134.1:c.2903A>C	XP_016870623.1:p.Glu968Ala
XM_017015136.2:c.2819A>C	XP_016870625.1:p.Glu940Ala
XM_017015137.1:c.2804A>C	XP_016870626.1:p.Glu935Ala
XM_017015138.1:c.2804A>C	XP_016870627.1:p.Glu935Ala
XM_024447674.1:c.2747A>C	XP_024303442.1:p.Glu916Ala
XM_024447675.1:c.2681A>C	XP_024303443.1:p.Glu894Ala
XM_024447676.1:c.2042A>C	XP_024303444.1:p.Glu681Ala
XM_024447677.1:c.2042A>C	XP_024303445.1:p.Glu681Ala
XM_024447680.1:c.2660A>C	XP_024303448.1:p.Glu887Ala
NM_024757.5:c.2918A>C MANE Select	NP_079033.4:p.Glu973Ala
NM_001354263.2:c.2897A>C	NP_001341192.1:p.Glu966Ala