Canonical Allele Identifier: CA1884657152
Gene: EHMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137758003A= , CM000671.2:g.137758003A= GRCh38
NC_000009.11:g.140652455A= , CM000671.1:g.140652455A= GRCh37
NC_000009.10:g.139772276A= NCBI36
NG_011776.1:g.144012A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.1493A= MANE Select ENSP00000417980.1:p.Gln498=
ENST00000629335.2:c.1493A= ENSP00000490056.1:p.Gln498=
ENST00000636027.1:c.1379A= ENSP00000489961.1:p.Gln460=
ENST00000637161.1:c.1400A= ENSP00000490328.1:p.Gln467=
ENST00000637261.1:c.1533A= ENSP00000490815.1:n.1533A=
ENST00000637977.1:c.1438A=
ENST00000638071.1:c.1120A=
ENST00000640639.1:c.662A= ENSP00000491823.1:p.Gln221=
ENST00000371394.6:c.*1228A= ENSP00000485945.1:n.*1228A=
ENST00000460843.5:c.1493A= ENSP00000417980.1:p.Gln498=
ENST00000462484.5:c.1493A= ENSP00000417328.1:p.Gln498=
ENST00000462942.3:c.350A= ENSP00000436107.1:p.Gln117=
ENST00000465566.2:c.185A= ENSP00000486261.1:p.Gln62=
ENST00000629808.2:c.586A=
NM_001145527.1:c.1493A= NP_001138999.1:p.Gln498=
NM_024757.4:c.1493A= NP_079033.4:p.Gln498=
XM_005266105.3:c.1484A= XP_005266162.1:p.Gln495=
XM_005266110.1:c.1400A= XP_005266167.1:p.Gln467=
XM_006717288.2:c.1475A= XP_006717351.1:p.Gln492=
XM_011519021.1:c.1502A= XP_011517323.1:p.Gln501=
XM_011519022.1:c.1499A= XP_011517324.1:p.Gln500=
XM_011519023.1:c.1481A= XP_011517325.1:p.Gln494=
XM_011519024.1:c.1424A= XP_011517326.1:p.Gln475=
XM_011519025.1:c.1400A= XP_011517327.1:p.Gln467=
XM_011519026.1:c.1502A= XP_011517328.1:p.Gln501=
XM_011519027.1:c.1502A= XP_011517329.1:p.Gln501=
XM_011519028.1:c.1502A= XP_011517330.1:p.Gln501=
XM_011519033.1:c.1481A= XP_011517335.1:p.Gln494=
NM_001354259.1:c.1400A= NP_001341188.1:p.Gln467=
NM_001354263.1:c.1472A= NP_001341192.1:p.Gln491=
NM_001354611.1:c.1493A= NP_001341540.1:p.Gln498=
NM_001354612.1:c.1400A= NP_001341541.1:p.Gln467=
XM_005266105.5:c.1484A= XP_005266162.1:p.Gln495=
XM_011519021.3:c.1502A= XP_011517323.1:p.Gln501=
XM_011519022.3:c.1499A= XP_011517324.1:p.Gln500=
XM_011519023.3:c.1481A= XP_011517325.1:p.Gln494=
XM_017015134.1:c.1478A= XP_016870623.1:p.Gln493=
XM_017015136.2:c.1394A= XP_016870625.1:p.Gln465=
XM_017015137.1:c.1379A= XP_016870626.1:p.Gln460=
XM_017015138.1:c.1379A= XP_016870627.1:p.Gln460=
XM_024447674.1:c.1322A= XP_024303442.1:p.Gln441=
XM_024447675.1:c.1400A= XP_024303443.1:p.Gln467=
XM_024447676.1:c.617A= XP_024303444.1:p.Gln206=
XM_024447677.1:c.617A= XP_024303445.1:p.Gln206=
XM_024447678.1:c.1400A= XP_024303446.1:p.Gln467=
XM_024447679.1:c.1400A= XP_024303447.1:p.Gln467=
XM_024447680.1:c.1379A= XP_024303448.1:p.Gln460=
NM_024757.5:c.1493A= MANE Select NP_079033.4:p.Gln498=
NM_001145527.2:c.1493A= NP_001138999.1:p.Gln498=
NM_001354259.2:c.1400A= NP_001341188.1:p.Gln467=
NM_001354263.2:c.1472A= NP_001341192.1:p.Gln491=
NM_001354611.2:c.1493A= NP_001341540.1:p.Gln498=
NM_001354612.2:c.1400A= NP_001341541.1:p.Gln467=