Canonical Allele Identifier: CA201805274
Gene: EHMT1 HGNC NCBI

Linked Data

dbSNP Id: rs137852719

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137777892_137777893insG , CM000671.2:g.137777892_137777893insG GRCh38
NC_000009.11:g.140672344_140672345insG , CM000671.1:g.140672344_140672345insG GRCh37
NC_000009.10:g.139792165_139792166insG NCBI36
NG_011776.1:g.163901_163902insG

Transcript Alleles

HGVS Amino-acid change
ENST00000460843.6:c.2029_2030insG MANE Select ENSP00000417980.1:p.Pro677ArgfsTer21
ENST00000636027.1:c.1915_1916insG ENSP00000489961.1:p.Pro639ArgfsTer21
ENST00000637161.1:c.1936_1937insG ENSP00000490328.1:p.Pro646ArgfsTer21
ENST00000637261.1:c.2069_2070insG ENSP00000490815.1:n.2069_2070insG
ENST00000638071.1:c.1656_1657insG
ENST00000371394.6:c.*1764_*1765insG ENSP00000485945.1:n.*1764_*1765insG
ENST00000460843.5:c.2029_2030insG ENSP00000417980.1:p.Pro677ArgfsTer21
ENST00000462484.5:c.2029_2030insG ENSP00000417328.1:p.Pro677ArgfsTer21
ENST00000462942.3:c.886_887insG ENSP00000436107.1:p.Pro296ArgfsTer21
ENST00000626603.1:n.1061-505_1061-504insC
NM_001145527.1:c.2029_2030insG NP_001138999.1:p.Pro677ArgfsTer21
NM_024757.4:c.2029_2030insG NP_079033.4:p.Pro677ArgfsTer21
XM_005266105.3:c.2020_2021insG XP_005266162.1:p.Pro674ArgfsTer21
XM_005266110.1:c.1936_1937insG XP_005266167.1:p.Pro646ArgfsTer21
XM_006717288.2:c.2011_2012insG XP_006717351.1:p.Pro671ArgfsTer21
XM_011519021.1:c.2038_2039insG XP_011517323.1:p.Pro680ArgfsTer21
XM_011519022.1:c.2035_2036insG XP_011517324.1:p.Pro679ArgfsTer21
XM_011519023.1:c.2017_2018insG XP_011517325.1:p.Pro673ArgfsTer21
XM_011519024.1:c.1960_1961insG XP_011517326.1:p.Pro654ArgfsTer21
XM_011519025.1:c.1936_1937insG XP_011517327.1:p.Pro646ArgfsTer21
XM_011519026.1:c.1894_1895insG XP_011517328.1:p.Pro632ArgfsTer21
XM_011519027.1:c.2038_2039insG XP_011517329.1:p.Pro680ArgfsTer21
XM_011519028.1:c.2038_2039insG XP_011517330.1:p.Pro680ArgfsTer21
XM_011519029.1:c.460_461insG XP_011517331.1:p.Pro154ArgfsTer21
XM_011519033.1:c.1873_1874insG XP_011517335.1:p.Pro625ArgfsTer21
NM_001354259.1:c.1936_1937insG NP_001341188.1:p.Pro646ArgfsTer21
NM_001354263.1:c.2008_2009insG NP_001341192.1:p.Pro670ArgfsTer21
XM_005266105.5:c.2020_2021insG XP_005266162.1:p.Pro674ArgfsTer21
XM_011519021.3:c.2038_2039insG XP_011517323.1:p.Pro680ArgfsTer21
XM_011519022.3:c.2035_2036insG XP_011517324.1:p.Pro679ArgfsTer21
XM_011519023.3:c.2017_2018insG XP_011517325.1:p.Pro673ArgfsTer21
XM_011519029.3:c.460_461insG XP_011517331.1:p.Pro154ArgfsTer21
XM_017015134.1:c.2014_2015insG XP_016870623.1:p.Pro672ArgfsTer21
XM_017015136.2:c.1930_1931insG XP_016870625.1:p.Pro644ArgfsTer21
XM_017015137.1:c.1915_1916insG XP_016870626.1:p.Pro639ArgfsTer21
XM_017015138.1:c.1915_1916insG XP_016870627.1:p.Pro639ArgfsTer21
XM_024447674.1:c.1858_1859insG XP_024303442.1:p.Pro620ArgfsTer21
XM_024447675.1:c.1792_1793insG XP_024303443.1:p.Pro598ArgfsTer21
XM_024447676.1:c.1153_1154insG XP_024303444.1:p.Pro385ArgfsTer21
XM_024447677.1:c.1153_1154insG XP_024303445.1:p.Pro385ArgfsTer21
XM_024447678.1:c.1936_1937insG XP_024303446.1:p.Pro646ArgfsTer21
XM_024447679.1:c.1936_1937insG XP_024303447.1:p.Pro646ArgfsTer21
XM_024447680.1:c.1771_1772insG XP_024303448.1:p.Pro591ArgfsTer21
NM_024757.5:c.2029_2030insG MANE Select NP_079033.4:p.Pro677ArgfsTer21
NM_001145527.2:c.2029_2030insG NP_001138999.1:p.Pro677ArgfsTer21
NM_001354259.2:c.1936_1937insG NP_001341188.1:p.Pro646ArgfsTer21
NM_001354263.2:c.2008_2009insG NP_001341192.1:p.Pro670ArgfsTer21