Canonical Allele Identifier: CA375793377

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707516C>A (hg19) ; chr9:g.137813064C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813064C>A , CM000671.2:g.137813064C>A	GRCh38
NC_000009.11:g.140707516C>A , CM000671.1:g.140707516C>A	GRCh37
NC_000009.10:g.139827337C>A	NCBI36
NG_011776.1:g.199073C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2926C>A MANE Select	ENSP00000417980.1:p.Leu976Met
ENST00000636027.1:c.2812C>A	ENSP00000489961.1:p.Leu938Met
ENST00000637161.1:c.2833C>A	ENSP00000490328.1:p.Leu945Met
ENST00000637261.1:c.2966C>A	ENSP00000490815.1:n.2966C>A
ENST00000637891.1:c.820C>A	ENSP00000490907.1:p.Leu274Met
ENST00000460843.5:c.2926C>A	ENSP00000417980.1:p.Leu976Met
ENST00000462942.3:c.1783C>A	ENSP00000436107.1:p.Leu595Met
ENST00000486164.5:c.613C>A
ENST00000488242.2:n.452C>A
NM_024757.4:c.2926C>A	NP_079033.4:p.Leu976Met
XM_005266105.3:c.2917C>A	XP_005266162.1:p.Leu973Met
XM_005266110.1:c.2833C>A	XP_005266167.1:p.Leu945Met
XM_006717288.2:c.2908C>A	XP_006717351.1:p.Leu970Met
XM_011519021.1:c.2935C>A	XP_011517323.1:p.Leu979Met
XM_011519022.1:c.2932C>A	XP_011517324.1:p.Leu978Met
XM_011519023.1:c.2914C>A	XP_011517325.1:p.Leu972Met
XM_011519024.1:c.2857C>A	XP_011517326.1:p.Leu953Met
XM_011519025.1:c.2833C>A	XP_011517327.1:p.Leu945Met
XM_011519026.1:c.2791C>A	XP_011517328.1:p.Leu931Met
XM_011519029.1:c.1357C>A	XP_011517331.1:p.Leu453Met
XM_011519030.1:c.709C>A	XP_011517332.1:p.Leu237Met
XM_011519031.1:c.496C>A	XP_011517333.1:p.Leu166Met
XM_011519032.1:c.496C>A	XP_011517334.1:p.Leu166Met
XM_011519033.1:c.2770C>A	XP_011517335.1:p.Leu924Met
NM_001354263.1:c.2905C>A	NP_001341192.1:p.Leu969Met
XM_005266105.5:c.2917C>A	XP_005266162.1:p.Leu973Met
XM_011519021.3:c.2935C>A	XP_011517323.1:p.Leu979Met
XM_011519022.3:c.2932C>A	XP_011517324.1:p.Leu978Met
XM_011519023.3:c.2914C>A	XP_011517325.1:p.Leu972Met
XM_011519029.3:c.1357C>A	XP_011517331.1:p.Leu453Met
XM_011519030.3:c.709C>A	XP_011517332.1:p.Leu237Met
XM_017015134.1:c.2911C>A	XP_016870623.1:p.Leu971Met
XM_017015136.2:c.2827C>A	XP_016870625.1:p.Leu943Met
XM_017015137.1:c.2812C>A	XP_016870626.1:p.Leu938Met
XM_017015138.1:c.2812C>A	XP_016870627.1:p.Leu938Met
XM_024447674.1:c.2755C>A	XP_024303442.1:p.Leu919Met
XM_024447675.1:c.2689C>A	XP_024303443.1:p.Leu897Met
XM_024447676.1:c.2050C>A	XP_024303444.1:p.Leu684Met
XM_024447677.1:c.2050C>A	XP_024303445.1:p.Leu684Met
XM_024447680.1:c.2668C>A	XP_024303448.1:p.Leu890Met
NM_024757.5:c.2926C>A MANE Select	NP_079033.4:p.Leu976Met
NM_001354263.2:c.2905C>A	NP_001341192.1:p.Leu969Met