Canonical Allele Identifier: CA375793359

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707507G>T (hg19) ; chr9:g.137813055G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813055G>T , CM000671.2:g.137813055G>T	GRCh38
NC_000009.11:g.140707507G>T , CM000671.1:g.140707507G>T	GRCh37
NC_000009.10:g.139827328G>T	NCBI36
NG_011776.1:g.199064G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2917G>T MANE Select	ENSP00000417980.1:p.Glu973Ter
ENST00000636027.1:c.2803G>T	ENSP00000489961.1:p.Glu935Ter
ENST00000637161.1:c.2824G>T	ENSP00000490328.1:p.Glu942Ter
ENST00000637261.1:c.2957G>T	ENSP00000490815.1:n.2957G>T
ENST00000637891.1:c.811G>T	ENSP00000490907.1:p.Glu271Ter
ENST00000460843.5:c.2917G>T	ENSP00000417980.1:p.Glu973Ter
ENST00000462942.3:c.1774G>T	ENSP00000436107.1:p.Glu592Ter
ENST00000486164.5:c.604G>T
ENST00000488242.2:n.443G>T
NM_024757.4:c.2917G>T	NP_079033.4:p.Glu973Ter
XM_005266105.3:c.2908G>T	XP_005266162.1:p.Glu970Ter
XM_005266110.1:c.2824G>T	XP_005266167.1:p.Glu942Ter
XM_006717288.2:c.2899G>T	XP_006717351.1:p.Glu967Ter
XM_011519021.1:c.2926G>T	XP_011517323.1:p.Glu976Ter
XM_011519022.1:c.2923G>T	XP_011517324.1:p.Glu975Ter
XM_011519023.1:c.2905G>T	XP_011517325.1:p.Glu969Ter
XM_011519024.1:c.2848G>T	XP_011517326.1:p.Glu950Ter
XM_011519025.1:c.2824G>T	XP_011517327.1:p.Glu942Ter
XM_011519026.1:c.2782G>T	XP_011517328.1:p.Glu928Ter
XM_011519029.1:c.1348G>T	XP_011517331.1:p.Glu450Ter
XM_011519030.1:c.700G>T	XP_011517332.1:p.Glu234Ter
XM_011519031.1:c.487G>T	XP_011517333.1:p.Glu163Ter
XM_011519032.1:c.487G>T	XP_011517334.1:p.Glu163Ter
XM_011519033.1:c.2761G>T	XP_011517335.1:p.Glu921Ter
NM_001354263.1:c.2896G>T	NP_001341192.1:p.Glu966Ter
XM_005266105.5:c.2908G>T	XP_005266162.1:p.Glu970Ter
XM_011519021.3:c.2926G>T	XP_011517323.1:p.Glu976Ter
XM_011519022.3:c.2923G>T	XP_011517324.1:p.Glu975Ter
XM_011519023.3:c.2905G>T	XP_011517325.1:p.Glu969Ter
XM_011519029.3:c.1348G>T	XP_011517331.1:p.Glu450Ter
XM_011519030.3:c.700G>T	XP_011517332.1:p.Glu234Ter
XM_017015134.1:c.2902G>T	XP_016870623.1:p.Glu968Ter
XM_017015136.2:c.2818G>T	XP_016870625.1:p.Glu940Ter
XM_017015137.1:c.2803G>T	XP_016870626.1:p.Glu935Ter
XM_017015138.1:c.2803G>T	XP_016870627.1:p.Glu935Ter
XM_024447674.1:c.2746G>T	XP_024303442.1:p.Glu916Ter
XM_024447675.1:c.2680G>T	XP_024303443.1:p.Glu894Ter
XM_024447676.1:c.2041G>T	XP_024303444.1:p.Glu681Ter
XM_024447677.1:c.2041G>T	XP_024303445.1:p.Glu681Ter
XM_024447680.1:c.2659G>T	XP_024303448.1:p.Glu887Ter
NM_024757.5:c.2917G>T MANE Select	NP_079033.4:p.Glu973Ter
NM_001354263.2:c.2896G>T	NP_001341192.1:p.Glu966Ter