Canonical Allele Identifier: CA1884685778
Gene: EHMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137813240_137813241delinsGA , CM000671.2:g.137813240_137813241delinsGA GRCh38
NC_000009.11:g.140707692_140707693delinsGA , CM000671.1:g.140707692_140707693delinsGA GRCh37
NC_000009.10:g.139827513_139827514delinsGA NCBI36
NG_011776.1:g.199249_199250delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.3035+67_3035+68delinsGA MANE Select ENSP00000417980.1:n.3035+67_3035+68delinsGA
ENST00000636027.1:c.2921+67_2921+68delinsGA ENSP00000489961.1:n.2921+67_2921+68delinsGA
ENST00000637161.1:c.2942+67_2942+68delinsGA ENSP00000490328.1:n.2942+67_2942+68delinsGA
ENST00000637261.1:c.3075+67_3075+68delinsGA ENSP00000490815.1:n.3075+67_3075+68delinsGA
ENST00000637891.1:c.929+67_929+68delinsGA ENSP00000490907.1:n.929+67_929+68delinsGA
ENST00000460843.5:c.3035+67_3035+68delinsGA ENSP00000417980.1:n.3035+67_3035+68delinsGA
ENST00000462942.3:c.1892+67_1892+68delinsGA ENSP00000436107.1:n.1892+67_1892+68delinsGA
ENST00000486164.5:c.722+67_722+68delinsGA
ENST00000488242.2:n.561+67_561+68delinsGA
NM_024757.4:c.3035+67_3035+68delinsGA NP_079033.4:n.3035+67_3035+68delinsGA
XM_005266105.3:c.3026+67_3026+68delinsGA XP_005266162.1:n.3026+67_3026+68delinsGA
XM_005266110.1:c.2942+67_2942+68delinsGA XP_005266167.1:n.2942+67_2942+68delinsGA
XM_006717288.2:c.3017+67_3017+68delinsGA XP_006717351.1:n.3017+67_3017+68delinsGA
XM_011519021.1:c.3044+67_3044+68delinsGA XP_011517323.1:n.3044+67_3044+68delinsGA
XM_011519022.1:c.3041+67_3041+68delinsGA XP_011517324.1:n.3041+67_3041+68delinsGA
XM_011519023.1:c.3023+67_3023+68delinsGA XP_011517325.1:n.3023+67_3023+68delinsGA
XM_011519024.1:c.2966+67_2966+68delinsGA XP_011517326.1:n.2966+67_2966+68delinsGA
XM_011519025.1:c.2942+67_2942+68delinsGA XP_011517327.1:n.2942+67_2942+68delinsGA
XM_011519026.1:c.2900+67_2900+68delinsGA XP_011517328.1:n.2900+67_2900+68delinsGA
XM_011519029.1:c.1466+67_1466+68delinsGA XP_011517331.1:n.1466+67_1466+68delinsGA
XM_011519030.1:c.818+67_818+68delinsGA XP_011517332.1:n.818+67_818+68delinsGA
XM_011519031.1:c.605+67_605+68delinsGA XP_011517333.1:n.605+67_605+68delinsGA
XM_011519032.1:c.605+67_605+68delinsGA XP_011517334.1:n.605+67_605+68delinsGA
XM_011519033.1:c.2879+67_2879+68delinsGA XP_011517335.1:n.2879+67_2879+68delinsGA
NM_001354263.1:c.3014+67_3014+68delinsGA NP_001341192.1:n.3014+67_3014+68delinsGA
XM_005266105.5:c.3026+67_3026+68delinsGA XP_005266162.1:n.3026+67_3026+68delinsGA
XM_011519021.3:c.3044+67_3044+68delinsGA XP_011517323.1:n.3044+67_3044+68delinsGA
XM_011519022.3:c.3041+67_3041+68delinsGA XP_011517324.1:n.3041+67_3041+68delinsGA
XM_011519023.3:c.3023+67_3023+68delinsGA XP_011517325.1:n.3023+67_3023+68delinsGA
XM_011519029.3:c.1466+67_1466+68delinsGA XP_011517331.1:n.1466+67_1466+68delinsGA
XM_011519030.3:c.818+67_818+68delinsGA XP_011517332.1:n.818+67_818+68delinsGA
XM_017015134.1:c.3020+67_3020+68delinsGA XP_016870623.1:n.3020+67_3020+68delinsGA
XM_017015136.2:c.2936+67_2936+68delinsGA XP_016870625.1:n.2936+67_2936+68delinsGA
XM_017015137.1:c.2921+67_2921+68delinsGA XP_016870626.1:n.2921+67_2921+68delinsGA
XM_017015138.1:c.2921+67_2921+68delinsGA XP_016870627.1:n.2921+67_2921+68delinsGA
XM_024447674.1:c.2864+67_2864+68delinsGA XP_024303442.1:n.2864+67_2864+68delinsGA
XM_024447675.1:c.2798+67_2798+68delinsGA XP_024303443.1:n.2798+67_2798+68delinsGA
XM_024447676.1:c.2159+67_2159+68delinsGA XP_024303444.1:n.2159+67_2159+68delinsGA
XM_024447677.1:c.2159+67_2159+68delinsGA XP_024303445.1:n.2159+67_2159+68delinsGA
XM_024447680.1:c.2777+67_2777+68delinsGA XP_024303448.1:n.2777+67_2777+68delinsGA
NM_024757.5:c.3035+67_3035+68delinsGA MANE Select NP_079033.4:n.3035+67_3035+68delinsGA
NM_001354263.2:c.3014+67_3014+68delinsGA NP_001341192.1:n.3014+67_3014+68delinsGA