Canonical Allele Identifier: CA375776511
Gene: EHMT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137776748C>G , CM000671.2:g.137776748C>G GRCh38
NC_000009.11:g.140671200C>G , CM000671.1:g.140671200C>G GRCh37
NC_000009.10:g.139791021C>G NCBI36
NG_011776.1:g.162757C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.1922C>G MANE Select ENSP00000417980.1:p.Thr641Arg
ENST00000636027.1:c.1808C>G ENSP00000489961.1:p.Thr603Arg
ENST00000637161.1:c.1829C>G ENSP00000490328.1:p.Thr610Arg
ENST00000637261.1:c.1962C>G ENSP00000490815.1:n.1962C>G
ENST00000638071.1:c.1549C>G
ENST00000640639.1:c.1091C>G ENSP00000491823.1:p.Thr364Arg
ENST00000371394.6:c.*1657C>G ENSP00000485945.1:n.*1657C>G
ENST00000460843.5:c.1922C>G ENSP00000417980.1:p.Thr641Arg
ENST00000462484.5:c.1922C>G ENSP00000417328.1:p.Thr641Arg
ENST00000462942.3:c.779C>G ENSP00000436107.1:p.Thr260Arg
ENST00000465566.2:c.470C>G ENSP00000486261.1:p.Thr157Arg
ENST00000626603.1:n.1701G>C
NM_001145527.1:c.1922C>G NP_001138999.1:p.Thr641Arg
NM_024757.4:c.1922C>G NP_079033.4:p.Thr641Arg
XM_005266105.3:c.1913C>G XP_005266162.1:p.Thr638Arg
XM_005266110.1:c.1829C>G XP_005266167.1:p.Thr610Arg
XM_006717288.2:c.1904C>G XP_006717351.1:p.Thr635Arg
XM_011519021.1:c.1931C>G XP_011517323.1:p.Thr644Arg
XM_011519022.1:c.1928C>G XP_011517324.1:p.Thr643Arg
XM_011519023.1:c.1910C>G XP_011517325.1:p.Thr637Arg
XM_011519024.1:c.1853C>G XP_011517326.1:p.Thr618Arg
XM_011519025.1:c.1829C>G XP_011517327.1:p.Thr610Arg
XM_011519026.1:c.1787C>G XP_011517328.1:p.Thr596Arg
XM_011519027.1:c.1931C>G XP_011517329.1:p.Thr644Arg
XM_011519028.1:c.1931C>G XP_011517330.1:p.Thr644Arg
XM_011519029.1:c.353C>G XP_011517331.1:p.Thr118Arg
XM_011519033.1:c.1766C>G XP_011517335.1:p.Thr589Arg
NM_001354259.1:c.1829C>G NP_001341188.1:p.Thr610Arg
NM_001354263.1:c.1901C>G NP_001341192.1:p.Thr634Arg
XM_005266105.5:c.1913C>G XP_005266162.1:p.Thr638Arg
XM_011519021.3:c.1931C>G XP_011517323.1:p.Thr644Arg
XM_011519022.3:c.1928C>G XP_011517324.1:p.Thr643Arg
XM_011519023.3:c.1910C>G XP_011517325.1:p.Thr637Arg
XM_011519029.3:c.353C>G XP_011517331.1:p.Thr118Arg
XM_017015134.1:c.1907C>G XP_016870623.1:p.Thr636Arg
XM_017015136.2:c.1823C>G XP_016870625.1:p.Thr608Arg
XM_017015137.1:c.1808C>G XP_016870626.1:p.Thr603Arg
XM_017015138.1:c.1808C>G XP_016870627.1:p.Thr603Arg
XM_024447674.1:c.1751C>G XP_024303442.1:p.Thr584Arg
XM_024447675.1:c.1685C>G XP_024303443.1:p.Thr562Arg
XM_024447676.1:c.1046C>G XP_024303444.1:p.Thr349Arg
XM_024447677.1:c.1046C>G XP_024303445.1:p.Thr349Arg
XM_024447678.1:c.1829C>G XP_024303446.1:p.Thr610Arg
XM_024447679.1:c.1829C>G XP_024303447.1:p.Thr610Arg
XM_024447680.1:c.1664C>G XP_024303448.1:p.Thr555Arg
NM_024757.5:c.1922C>G MANE Select NP_079033.4:p.Thr641Arg
NM_001145527.2:c.1922C>G NP_001138999.1:p.Thr641Arg
NM_001354259.2:c.1829C>G NP_001341188.1:p.Thr610Arg
NM_001354263.2:c.1901C>G NP_001341192.1:p.Thr634Arg