Canonical Allele Identifier: CA2842411109
Gene: EHMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137813422dup , CM000671.2:g.137813422dup GRCh38
NC_000009.11:g.140707874dup , CM000671.1:g.140707874dup GRCh37
NC_000009.10:g.139827695dup NCBI36
NG_011776.1:g.199431dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.3072dup MANE Select ENSP00000417980.1:p.Cys1025LeufsTer?
ENST00000637161.1:c.2979dup ENSP00000490328.1:p.Cys994LeufsTer?
ENST00000637261.1:c.3112dup ENSP00000490815.1:n.3112dup
ENST00000637891.1:c.966dup ENSP00000490907.1:p.Cys323LeufsTer?
ENST00000460843.5:c.3072dup ENSP00000417980.1:p.Cys1025LeufsTer?
ENST00000462942.3:c.1929dup ENSP00000436107.1:p.Cys644LeufsTer?
ENST00000486164.5:c.759dup
ENST00000488242.2:n.598dup
NM_024757.4:c.3072dup NP_079033.4:p.Cys1025LeufsTer?
XM_005266105.3:c.3063dup XP_005266162.1:p.Cys1022LeufsTer?
XM_005266110.1:c.2979dup XP_005266167.1:p.Cys994LeufsTer?
XM_006717288.2:c.3054dup XP_006717351.1:p.Cys1019LeufsTer?
XM_011519021.1:c.3081dup XP_011517323.1:p.Cys1028LeufsTer?
XM_011519022.1:c.3078dup XP_011517324.1:p.Cys1027LeufsTer?
XM_011519023.1:c.3060dup XP_011517325.1:p.Cys1021LeufsTer?
XM_011519024.1:c.3003dup XP_011517326.1:p.Cys1002LeufsTer?
XM_011519025.1:c.2979dup XP_011517327.1:p.Cys994LeufsTer?
XM_011519026.1:c.2937dup XP_011517328.1:p.Cys980LeufsTer?
XM_011519029.1:c.1503dup XP_011517331.1:p.Cys502LeufsTer?
XM_011519030.1:c.855dup XP_011517332.1:p.Cys286LeufsTer?
XM_011519031.1:c.642dup XP_011517333.1:p.Cys215LeufsTer?
XM_011519032.1:c.642dup XP_011517334.1:p.Cys215LeufsTer?
XM_011519033.1:c.2916dup XP_011517335.1:p.Cys973LeufsTer?
NM_001354263.1:c.3051dup NP_001341192.1:p.Cys1018LeufsTer?
XM_005266105.5:c.3063dup XP_005266162.1:p.Cys1022LeufsTer?
XM_011519021.3:c.3081dup XP_011517323.1:p.Cys1028LeufsTer?
XM_011519022.3:c.3078dup XP_011517324.1:p.Cys1027LeufsTer?
XM_011519023.3:c.3060dup XP_011517325.1:p.Cys1021LeufsTer?
XM_011519029.3:c.1503dup XP_011517331.1:p.Cys502LeufsTer?
XM_011519030.3:c.855dup XP_011517332.1:p.Cys286LeufsTer?
XM_017015134.1:c.3057dup XP_016870623.1:p.Cys1020LeufsTer?
XM_017015136.2:c.2973dup XP_016870625.1:p.Cys992LeufsTer?
XM_017015137.1:c.2958dup XP_016870626.1:p.Cys987LeufsTer?
XM_017015138.1:c.2958dup XP_016870627.1:p.Cys987LeufsTer?
XM_024447674.1:c.2901dup XP_024303442.1:p.Cys968LeufsTer?
XM_024447675.1:c.2835dup XP_024303443.1:p.Cys946LeufsTer?
XM_024447676.1:c.2196dup XP_024303444.1:p.Cys733LeufsTer?
XM_024447677.1:c.2196dup XP_024303445.1:p.Cys733LeufsTer?
XM_024447680.1:c.2814dup XP_024303448.1:p.Cys939LeufsTer?
NM_024757.5:c.3072dup MANE Select NP_079033.4:p.Cys1025LeufsTer?
NM_001354263.2:c.3051dup NP_001341192.1:p.Cys1018LeufsTer?