Canonical Allele Identifier: CA467878170

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707940G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813488G>T , CM000671.2:g.137813488G>T	GRCh38
NC_000009.11:g.140707940G>T , CM000671.1:g.140707940G>T	GRCh37
NC_000009.10:g.139827761G>T	NCBI36
NG_011776.1:g.199497G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3138G>T MANE Select	ENSP00000417980.1:p.Val1046=
ENST00000637161.1:c.3045G>T	ENSP00000490328.1:p.Val1015=
ENST00000637261.1:c.3178G>T	ENSP00000490815.1:n.3178G>T
ENST00000637891.1:c.1032G>T	ENSP00000490907.1:p.Val344=
ENST00000460843.5:c.3138G>T	ENSP00000417980.1:p.Val1046=
ENST00000462942.3:c.1995G>T	ENSP00000436107.1:p.Val665=
ENST00000488242.2:n.664G>T
NM_024757.4:c.3138G>T	NP_079033.4:p.Val1046=
XM_005266105.3:c.3129G>T	XP_005266162.1:p.Val1043=
XM_005266110.1:c.3045G>T	XP_005266167.1:p.Val1015=
XM_006717288.2:c.3120G>T	XP_006717351.1:p.Val1040=
XM_011519021.1:c.3147G>T	XP_011517323.1:p.Val1049=
XM_011519022.1:c.3144G>T	XP_011517324.1:p.Val1048=
XM_011519023.1:c.3126G>T	XP_011517325.1:p.Val1042=
XM_011519024.1:c.3069G>T	XP_011517326.1:p.Val1023=
XM_011519025.1:c.3045G>T	XP_011517327.1:p.Val1015=
XM_011519026.1:c.3003G>T	XP_011517328.1:p.Val1001=
XM_011519029.1:c.1569G>T	XP_011517331.1:p.Val523=
XM_011519030.1:c.921G>T	XP_011517332.1:p.Val307=
XM_011519031.1:c.708G>T	XP_011517333.1:p.Val236=
XM_011519032.1:c.708G>T	XP_011517334.1:p.Val236=
XM_011519033.1:c.2982G>T	XP_011517335.1:p.Val994=
NM_001354263.1:c.3117G>T	NP_001341192.1:p.Val1039=
XM_005266105.5:c.3129G>T	XP_005266162.1:p.Val1043=
XM_011519021.3:c.3147G>T	XP_011517323.1:p.Val1049=
XM_011519022.3:c.3144G>T	XP_011517324.1:p.Val1048=
XM_011519023.3:c.3126G>T	XP_011517325.1:p.Val1042=
XM_011519029.3:c.1569G>T	XP_011517331.1:p.Val523=
XM_011519030.3:c.921G>T	XP_011517332.1:p.Val307=
XM_017015134.1:c.3123G>T	XP_016870623.1:p.Val1041=
XM_017015136.2:c.3039G>T	XP_016870625.1:p.Val1013=
XM_017015137.1:c.3024G>T	XP_016870626.1:p.Val1008=
XM_017015138.1:c.3024G>T	XP_016870627.1:p.Val1008=
XM_024447674.1:c.2967G>T	XP_024303442.1:p.Val989=
XM_024447675.1:c.2901G>T	XP_024303443.1:p.Val967=
XM_024447676.1:c.2262G>T	XP_024303444.1:p.Val754=
XM_024447677.1:c.2262G>T	XP_024303445.1:p.Val754=
XM_024447680.1:c.2880G>T	XP_024303448.1:p.Val960=
NM_024757.5:c.3138G>T MANE Select	NP_079033.4:p.Val1046=
NM_001354263.2:c.3117G>T	NP_001341192.1:p.Val1039=