Canonical Allele Identifier: CA375793632

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707574T>G (hg19) ; chr9:g.137813122T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813122T>G , CM000671.2:g.137813122T>G	GRCh38
NC_000009.11:g.140707574T>G , CM000671.1:g.140707574T>G	GRCh37
NC_000009.10:g.139827395T>G	NCBI36
NG_011776.1:g.199131T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2984T>G MANE Select	ENSP00000417980.1:p.Leu995Arg
ENST00000636027.1:c.2870T>G	ENSP00000489961.1:p.Leu957Arg
ENST00000637161.1:c.2891T>G	ENSP00000490328.1:p.Leu964Arg
ENST00000637261.1:c.3024T>G	ENSP00000490815.1:n.3024T>G
ENST00000637891.1:c.878T>G	ENSP00000490907.1:p.Leu293Arg
ENST00000460843.5:c.2984T>G	ENSP00000417980.1:p.Leu995Arg
ENST00000462942.3:c.1841T>G	ENSP00000436107.1:p.Leu614Arg
ENST00000486164.5:c.671T>G
ENST00000488242.2:n.510T>G
NM_024757.4:c.2984T>G	NP_079033.4:p.Leu995Arg
XM_005266105.3:c.2975T>G	XP_005266162.1:p.Leu992Arg
XM_005266110.1:c.2891T>G	XP_005266167.1:p.Leu964Arg
XM_006717288.2:c.2966T>G	XP_006717351.1:p.Leu989Arg
XM_011519021.1:c.2993T>G	XP_011517323.1:p.Leu998Arg
XM_011519022.1:c.2990T>G	XP_011517324.1:p.Leu997Arg
XM_011519023.1:c.2972T>G	XP_011517325.1:p.Leu991Arg
XM_011519024.1:c.2915T>G	XP_011517326.1:p.Leu972Arg
XM_011519025.1:c.2891T>G	XP_011517327.1:p.Leu964Arg
XM_011519026.1:c.2849T>G	XP_011517328.1:p.Leu950Arg
XM_011519029.1:c.1415T>G	XP_011517331.1:p.Leu472Arg
XM_011519030.1:c.767T>G	XP_011517332.1:p.Leu256Arg
XM_011519031.1:c.554T>G	XP_011517333.1:p.Leu185Arg
XM_011519032.1:c.554T>G	XP_011517334.1:p.Leu185Arg
XM_011519033.1:c.2828T>G	XP_011517335.1:p.Leu943Arg
NM_001354263.1:c.2963T>G	NP_001341192.1:p.Leu988Arg
XM_005266105.5:c.2975T>G	XP_005266162.1:p.Leu992Arg
XM_011519021.3:c.2993T>G	XP_011517323.1:p.Leu998Arg
XM_011519022.3:c.2990T>G	XP_011517324.1:p.Leu997Arg
XM_011519023.3:c.2972T>G	XP_011517325.1:p.Leu991Arg
XM_011519029.3:c.1415T>G	XP_011517331.1:p.Leu472Arg
XM_011519030.3:c.767T>G	XP_011517332.1:p.Leu256Arg
XM_017015134.1:c.2969T>G	XP_016870623.1:p.Leu990Arg
XM_017015136.2:c.2885T>G	XP_016870625.1:p.Leu962Arg
XM_017015137.1:c.2870T>G	XP_016870626.1:p.Leu957Arg
XM_017015138.1:c.2870T>G	XP_016870627.1:p.Leu957Arg
XM_024447674.1:c.2813T>G	XP_024303442.1:p.Leu938Arg
XM_024447675.1:c.2747T>G	XP_024303443.1:p.Leu916Arg
XM_024447676.1:c.2108T>G	XP_024303444.1:p.Leu703Arg
XM_024447677.1:c.2108T>G	XP_024303445.1:p.Leu703Arg
XM_024447680.1:c.2726T>G	XP_024303448.1:p.Leu909Arg
NM_024757.5:c.2984T>G MANE Select	NP_079033.4:p.Leu995Arg
NM_001354263.2:c.2963T>G	NP_001341192.1:p.Leu988Arg