Canonical Allele Identifier: CA375788910

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695387T>G (hg19) ; chr9:g.137800935T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800935T>G , CM000671.2:g.137800935T>G	GRCh38
NC_000009.11:g.140695387T>G , CM000671.1:g.140695387T>G	GRCh37
NC_000009.10:g.139815208T>G	NCBI36
NG_011776.1:g.186944T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2663T>G MANE Select	ENSP00000417980.1:p.Leu888Arg
ENST00000636027.1:c.2549T>G	ENSP00000489961.1:p.Leu850Arg
ENST00000637161.1:c.2570T>G	ENSP00000490328.1:p.Leu857Arg
ENST00000637261.1:c.2703T>G	ENSP00000490815.1:n.2703T>G
ENST00000637891.1:c.557T>G	ENSP00000490907.1:p.Leu186Arg
ENST00000637949.1:c.341T>G	ENSP00000489786.1:p.Leu114Arg
ENST00000460843.5:c.2663T>G	ENSP00000417980.1:p.Leu888Arg
ENST00000462942.3:c.1520T>G	ENSP00000436107.1:p.Leu507Arg
ENST00000482340.5:c.233T>G	ENSP00000486748.1:p.Leu78Arg
ENST00000486164.5:c.241T>G
ENST00000488242.2:n.189T>G
ENST00000493484.5:c.233T>G	ENSP00000486503.1:p.Leu78Arg
NM_024757.4:c.2663T>G	NP_079033.4:p.Leu888Arg
XM_005266105.3:c.2654T>G	XP_005266162.1:p.Leu885Arg
XM_005266110.1:c.2570T>G	XP_005266167.1:p.Leu857Arg
XM_006717288.2:c.2645T>G	XP_006717351.1:p.Leu882Arg
XM_011519021.1:c.2672T>G	XP_011517323.1:p.Leu891Arg
XM_011519022.1:c.2669T>G	XP_011517324.1:p.Leu890Arg
XM_011519023.1:c.2651T>G	XP_011517325.1:p.Leu884Arg
XM_011519024.1:c.2594T>G	XP_011517326.1:p.Leu865Arg
XM_011519025.1:c.2570T>G	XP_011517327.1:p.Leu857Arg
XM_011519026.1:c.2528T>G	XP_011517328.1:p.Leu843Arg
XM_011519027.1:c.2672T>G	XP_011517329.1:p.Leu891Arg
XM_011519029.1:c.1094T>G	XP_011517331.1:p.Leu365Arg
XM_011519030.1:c.446T>G	XP_011517332.1:p.Leu149Arg
XM_011519031.1:c.233T>G	XP_011517333.1:p.Leu78Arg
XM_011519032.1:c.233T>G	XP_011517334.1:p.Leu78Arg
XM_011519033.1:c.2507T>G	XP_011517335.1:p.Leu836Arg
NM_001354263.1:c.2642T>G	NP_001341192.1:p.Leu881Arg
XM_005266105.5:c.2654T>G	XP_005266162.1:p.Leu885Arg
XM_011519021.3:c.2672T>G	XP_011517323.1:p.Leu891Arg
XM_011519022.3:c.2669T>G	XP_011517324.1:p.Leu890Arg
XM_011519023.3:c.2651T>G	XP_011517325.1:p.Leu884Arg
XM_011519029.3:c.1094T>G	XP_011517331.1:p.Leu365Arg
XM_011519030.3:c.446T>G	XP_011517332.1:p.Leu149Arg
XM_017015134.1:c.2648T>G	XP_016870623.1:p.Leu883Arg
XM_017015136.2:c.2564T>G	XP_016870625.1:p.Leu855Arg
XM_017015137.1:c.2549T>G	XP_016870626.1:p.Leu850Arg
XM_017015138.1:c.2549T>G	XP_016870627.1:p.Leu850Arg
XM_024447674.1:c.2492T>G	XP_024303442.1:p.Leu831Arg
XM_024447675.1:c.2426T>G	XP_024303443.1:p.Leu809Arg
XM_024447676.1:c.1787T>G	XP_024303444.1:p.Leu596Arg
XM_024447677.1:c.1787T>G	XP_024303445.1:p.Leu596Arg
XM_024447678.1:c.2570T>G	XP_024303446.1:p.Leu857Arg
XM_024447680.1:c.2405T>G	XP_024303448.1:p.Leu802Arg
NM_024757.5:c.2663T>G MANE Select	NP_079033.4:p.Leu888Arg
NM_001354263.2:c.2642T>G	NP_001341192.1:p.Leu881Arg