Canonical Allele Identifier: CA375794177

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707913C>G (hg19) ; chr9:g.137813461C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813461C>G , CM000671.2:g.137813461C>G	GRCh38
NC_000009.11:g.140707913C>G , CM000671.1:g.140707913C>G	GRCh37
NC_000009.10:g.139827734C>G	NCBI36
NG_011776.1:g.199470C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3111C>G MANE Select	ENSP00000417980.1:p.Asn1037Lys
ENST00000637161.1:c.3018C>G	ENSP00000490328.1:p.Asn1006Lys
ENST00000637261.1:c.3151C>G	ENSP00000490815.1:n.3151C>G
ENST00000637891.1:c.1005C>G	ENSP00000490907.1:p.Asn335Lys
ENST00000460843.5:c.3111C>G	ENSP00000417980.1:p.Asn1037Lys
ENST00000462942.3:c.1968C>G	ENSP00000436107.1:p.Asn656Lys
ENST00000488242.2:n.637C>G
NM_024757.4:c.3111C>G	NP_079033.4:p.Asn1037Lys
XM_005266105.3:c.3102C>G	XP_005266162.1:p.Asn1034Lys
XM_005266110.1:c.3018C>G	XP_005266167.1:p.Asn1006Lys
XM_006717288.2:c.3093C>G	XP_006717351.1:p.Asn1031Lys
XM_011519021.1:c.3120C>G	XP_011517323.1:p.Asn1040Lys
XM_011519022.1:c.3117C>G	XP_011517324.1:p.Asn1039Lys
XM_011519023.1:c.3099C>G	XP_011517325.1:p.Asn1033Lys
XM_011519024.1:c.3042C>G	XP_011517326.1:p.Asn1014Lys
XM_011519025.1:c.3018C>G	XP_011517327.1:p.Asn1006Lys
XM_011519026.1:c.2976C>G	XP_011517328.1:p.Asn992Lys
XM_011519029.1:c.1542C>G	XP_011517331.1:p.Asn514Lys
XM_011519030.1:c.894C>G	XP_011517332.1:p.Asn298Lys
XM_011519031.1:c.681C>G	XP_011517333.1:p.Asn227Lys
XM_011519032.1:c.681C>G	XP_011517334.1:p.Asn227Lys
XM_011519033.1:c.2955C>G	XP_011517335.1:p.Asn985Lys
NM_001354263.1:c.3090C>G	NP_001341192.1:p.Asn1030Lys
XM_005266105.5:c.3102C>G	XP_005266162.1:p.Asn1034Lys
XM_011519021.3:c.3120C>G	XP_011517323.1:p.Asn1040Lys
XM_011519022.3:c.3117C>G	XP_011517324.1:p.Asn1039Lys
XM_011519023.3:c.3099C>G	XP_011517325.1:p.Asn1033Lys
XM_011519029.3:c.1542C>G	XP_011517331.1:p.Asn514Lys
XM_011519030.3:c.894C>G	XP_011517332.1:p.Asn298Lys
XM_017015134.1:c.3096C>G	XP_016870623.1:p.Asn1032Lys
XM_017015136.2:c.3012C>G	XP_016870625.1:p.Asn1004Lys
XM_017015137.1:c.2997C>G	XP_016870626.1:p.Asn999Lys
XM_017015138.1:c.2997C>G	XP_016870627.1:p.Asn999Lys
XM_024447674.1:c.2940C>G	XP_024303442.1:p.Asn980Lys
XM_024447675.1:c.2874C>G	XP_024303443.1:p.Asn958Lys
XM_024447676.1:c.2235C>G	XP_024303444.1:p.Asn745Lys
XM_024447677.1:c.2235C>G	XP_024303445.1:p.Asn745Lys
XM_024447680.1:c.2853C>G	XP_024303448.1:p.Asn951Lys
NM_024757.5:c.3111C>G MANE Select	NP_079033.4:p.Asn1037Lys
NM_001354263.2:c.3090C>G	NP_001341192.1:p.Asn1030Lys