Canonical Allele Identifier: CA375794493

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707953A>G (hg19) ; chr9:g.137813501A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813501A>G , CM000671.2:g.137813501A>G	GRCh38
NC_000009.11:g.140707953A>G , CM000671.1:g.140707953A>G	GRCh37
NC_000009.10:g.139827774A>G	NCBI36
NG_011776.1:g.199510A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3151A>G MANE Select	ENSP00000417980.1:p.Asn1051Asp
ENST00000637161.1:c.3058A>G	ENSP00000490328.1:p.Asn1020Asp
ENST00000637261.1:c.3191A>G	ENSP00000490815.1:n.3191A>G
ENST00000637891.1:c.1045A>G	ENSP00000490907.1:p.Asn349Asp
ENST00000460843.5:c.3151A>G	ENSP00000417980.1:p.Asn1051Asp
ENST00000462942.3:c.2008A>G	ENSP00000436107.1:p.Asn670Asp
ENST00000483653.1:n.11A>G
ENST00000488242.2:n.677A>G
NM_024757.4:c.3151A>G	NP_079033.4:p.Asn1051Asp
XM_005266105.3:c.3142A>G	XP_005266162.1:p.Asn1048Asp
XM_005266110.1:c.3058A>G	XP_005266167.1:p.Asn1020Asp
XM_006717288.2:c.3133A>G	XP_006717351.1:p.Asn1045Asp
XM_011519021.1:c.3160A>G	XP_011517323.1:p.Asn1054Asp
XM_011519022.1:c.3157A>G	XP_011517324.1:p.Asn1053Asp
XM_011519023.1:c.3139A>G	XP_011517325.1:p.Asn1047Asp
XM_011519024.1:c.3082A>G	XP_011517326.1:p.Asn1028Asp
XM_011519025.1:c.3058A>G	XP_011517327.1:p.Asn1020Asp
XM_011519026.1:c.3016A>G	XP_011517328.1:p.Asn1006Asp
XM_011519029.1:c.1582A>G	XP_011517331.1:p.Asn528Asp
XM_011519030.1:c.934A>G	XP_011517332.1:p.Asn312Asp
XM_011519031.1:c.721A>G	XP_011517333.1:p.Asn241Asp
XM_011519032.1:c.721A>G	XP_011517334.1:p.Asn241Asp
XM_011519033.1:c.2995A>G	XP_011517335.1:p.Asn999Asp
NM_001354263.1:c.3130A>G	NP_001341192.1:p.Asn1044Asp
XM_005266105.5:c.3142A>G	XP_005266162.1:p.Asn1048Asp
XM_011519021.3:c.3160A>G	XP_011517323.1:p.Asn1054Asp
XM_011519022.3:c.3157A>G	XP_011517324.1:p.Asn1053Asp
XM_011519023.3:c.3139A>G	XP_011517325.1:p.Asn1047Asp
XM_011519029.3:c.1582A>G	XP_011517331.1:p.Asn528Asp
XM_011519030.3:c.934A>G	XP_011517332.1:p.Asn312Asp
XM_017015134.1:c.3136A>G	XP_016870623.1:p.Asn1046Asp
XM_017015136.2:c.3052A>G	XP_016870625.1:p.Asn1018Asp
XM_017015137.1:c.3037A>G	XP_016870626.1:p.Asn1013Asp
XM_017015138.1:c.3037A>G	XP_016870627.1:p.Asn1013Asp
XM_024447674.1:c.2980A>G	XP_024303442.1:p.Asn994Asp
XM_024447675.1:c.2914A>G	XP_024303443.1:p.Asn972Asp
XM_024447676.1:c.2275A>G	XP_024303444.1:p.Asn759Asp
XM_024447677.1:c.2275A>G	XP_024303445.1:p.Asn759Asp
XM_024447680.1:c.2893A>G	XP_024303448.1:p.Asn965Asp
NM_024757.5:c.3151A>G MANE Select	NP_079033.4:p.Asn1051Asp
NM_001354263.2:c.3130A>G	NP_001341192.1:p.Asn1044Asp