Canonical Allele Identifier: CA1884685733
Gene: EHMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137813154G= , CM000671.2:g.137813154G= GRCh38
NC_000009.11:g.140707606G= , CM000671.1:g.140707606G= GRCh37
NC_000009.10:g.139827427G= NCBI36
NG_011776.1:g.199163G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.3016G= MANE Select ENSP00000417980.1:p.Val1006=
ENST00000636027.1:c.2902G= ENSP00000489961.1:p.Val968=
ENST00000637161.1:c.2923G= ENSP00000490328.1:p.Val975=
ENST00000637261.1:c.3056G= ENSP00000490815.1:n.3056G=
ENST00000637891.1:c.910G= ENSP00000490907.1:p.Val304=
ENST00000460843.5:c.3016G= ENSP00000417980.1:p.Val1006=
ENST00000462942.3:c.1873G= ENSP00000436107.1:p.Val625=
ENST00000486164.5:c.703G=
ENST00000488242.2:n.542G=
NM_024757.4:c.3016G= NP_079033.4:p.Val1006=
XM_005266105.3:c.3007G= XP_005266162.1:p.Val1003=
XM_005266110.1:c.2923G= XP_005266167.1:p.Val975=
XM_006717288.2:c.2998G= XP_006717351.1:p.Val1000=
XM_011519021.1:c.3025G= XP_011517323.1:p.Val1009=
XM_011519022.1:c.3022G= XP_011517324.1:p.Val1008=
XM_011519023.1:c.3004G= XP_011517325.1:p.Val1002=
XM_011519024.1:c.2947G= XP_011517326.1:p.Val983=
XM_011519025.1:c.2923G= XP_011517327.1:p.Val975=
XM_011519026.1:c.2881G= XP_011517328.1:p.Val961=
XM_011519029.1:c.1447G= XP_011517331.1:p.Val483=
XM_011519030.1:c.799G= XP_011517332.1:p.Val267=
XM_011519031.1:c.586G= XP_011517333.1:p.Val196=
XM_011519032.1:c.586G= XP_011517334.1:p.Val196=
XM_011519033.1:c.2860G= XP_011517335.1:p.Val954=
NM_001354263.1:c.2995G= NP_001341192.1:p.Val999=
XM_005266105.5:c.3007G= XP_005266162.1:p.Val1003=
XM_011519021.3:c.3025G= XP_011517323.1:p.Val1009=
XM_011519022.3:c.3022G= XP_011517324.1:p.Val1008=
XM_011519023.3:c.3004G= XP_011517325.1:p.Val1002=
XM_011519029.3:c.1447G= XP_011517331.1:p.Val483=
XM_011519030.3:c.799G= XP_011517332.1:p.Val267=
XM_017015134.1:c.3001G= XP_016870623.1:p.Val1001=
XM_017015136.2:c.2917G= XP_016870625.1:p.Val973=
XM_017015137.1:c.2902G= XP_016870626.1:p.Val968=
XM_017015138.1:c.2902G= XP_016870627.1:p.Val968=
XM_024447674.1:c.2845G= XP_024303442.1:p.Val949=
XM_024447675.1:c.2779G= XP_024303443.1:p.Val927=
XM_024447676.1:c.2140G= XP_024303444.1:p.Val714=
XM_024447677.1:c.2140G= XP_024303445.1:p.Val714=
XM_024447680.1:c.2758G= XP_024303448.1:p.Val920=
NM_024757.5:c.3016G= MANE Select NP_079033.4:p.Val1006=
NM_001354263.2:c.2995G= NP_001341192.1:p.Val999=