Canonical Allele Identifier: CA375793958

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707875T>G (hg19) ; chr9:g.137813423T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813423T>G , CM000671.2:g.137813423T>G	GRCh38
NC_000009.11:g.140707875T>G , CM000671.1:g.140707875T>G	GRCh37
NC_000009.10:g.139827696T>G	NCBI36
NG_011776.1:g.199432T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000460843.6:c.3073T>G MANE Select	ENSP00000417980.1:p.Cys1025Gly
ENST00000637161.1:c.2980T>G	ENSP00000490328.1:p.Cys994Gly
ENST00000637261.1:c.3113T>G	ENSP00000490815.1:n.3113T>G
ENST00000637891.1:c.967T>G	ENSP00000490907.1:p.Cys323Gly
ENST00000460843.5:c.3073T>G	ENSP00000417980.1:p.Cys1025Gly
ENST00000462942.3:c.1930T>G	ENSP00000436107.1:p.Cys644Gly
ENST00000486164.5:c.760T>G
ENST00000488242.2:n.599T>G
NM_024757.4:c.3073T>G	NP_079033.4:p.Cys1025Gly
XM_005266105.3:c.3064T>G	XP_005266162.1:p.Cys1022Gly
XM_005266110.1:c.2980T>G	XP_005266167.1:p.Cys994Gly
XM_006717288.2:c.3055T>G	XP_006717351.1:p.Cys1019Gly
XM_011519021.1:c.3082T>G	XP_011517323.1:p.Cys1028Gly
XM_011519022.1:c.3079T>G	XP_011517324.1:p.Cys1027Gly
XM_011519023.1:c.3061T>G	XP_011517325.1:p.Cys1021Gly
XM_011519024.1:c.3004T>G	XP_011517326.1:p.Cys1002Gly
XM_011519025.1:c.2980T>G	XP_011517327.1:p.Cys994Gly
XM_011519026.1:c.2938T>G	XP_011517328.1:p.Cys980Gly
XM_011519029.1:c.1504T>G	XP_011517331.1:p.Cys502Gly
XM_011519030.1:c.856T>G	XP_011517332.1:p.Cys286Gly
XM_011519031.1:c.643T>G	XP_011517333.1:p.Cys215Gly
XM_011519032.1:c.643T>G	XP_011517334.1:p.Cys215Gly
XM_011519033.1:c.2917T>G	XP_011517335.1:p.Cys973Gly
NM_001354263.1:c.3052T>G	NP_001341192.1:p.Cys1018Gly
XM_005266105.5:c.3064T>G	XP_005266162.1:p.Cys1022Gly
XM_011519021.3:c.3082T>G	XP_011517323.1:p.Cys1028Gly
XM_011519022.3:c.3079T>G	XP_011517324.1:p.Cys1027Gly
XM_011519023.3:c.3061T>G	XP_011517325.1:p.Cys1021Gly
XM_011519029.3:c.1504T>G	XP_011517331.1:p.Cys502Gly
XM_011519030.3:c.856T>G	XP_011517332.1:p.Cys286Gly
XM_017015134.1:c.3058T>G	XP_016870623.1:p.Cys1020Gly
XM_017015136.2:c.2974T>G	XP_016870625.1:p.Cys992Gly
XM_017015137.1:c.2959T>G	XP_016870626.1:p.Cys987Gly
XM_017015138.1:c.2959T>G	XP_016870627.1:p.Cys987Gly
XM_024447674.1:c.2902T>G	XP_024303442.1:p.Cys968Gly
XM_024447675.1:c.2836T>G	XP_024303443.1:p.Cys946Gly
XM_024447676.1:c.2197T>G	XP_024303444.1:p.Cys733Gly
XM_024447677.1:c.2197T>G	XP_024303445.1:p.Cys733Gly
XM_024447680.1:c.2815T>G	XP_024303448.1:p.Cys939Gly
NM_024757.5:c.3073T>G MANE Select	NP_079033.4:p.Cys1025Gly
NM_001354263.2:c.3052T>G	NP_001341192.1:p.Cys1018Gly