Canonical Allele Identifier: CA1884666502
Gene: EHMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137776745T= , CM000671.2:g.137776745T= GRCh38
NC_000009.11:g.140671197T= , CM000671.1:g.140671197T= GRCh37
NC_000009.10:g.139791018T= NCBI36
NG_011776.1:g.162754T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.1919T= MANE Select ENSP00000417980.1:p.Val640=
ENST00000636027.1:c.1805T= ENSP00000489961.1:p.Val602=
ENST00000637161.1:c.1826T= ENSP00000490328.1:p.Val609=
ENST00000637261.1:c.1959T= ENSP00000490815.1:n.1959T=
ENST00000638071.1:c.1546T=
ENST00000640639.1:c.1088T= ENSP00000491823.1:p.Val363=
ENST00000371394.6:c.*1654T= ENSP00000485945.1:n.*1654T=
ENST00000460843.5:c.1919T= ENSP00000417980.1:p.Val640=
ENST00000462484.5:c.1919T= ENSP00000417328.1:p.Val640=
ENST00000462942.3:c.776T= ENSP00000436107.1:p.Val259=
ENST00000465566.2:c.467T= ENSP00000486261.1:p.Val156=
ENST00000626603.1:n.1704A=
NM_001145527.1:c.1919T= NP_001138999.1:p.Val640=
NM_024757.4:c.1919T= NP_079033.4:p.Val640=
XM_005266105.3:c.1910T= XP_005266162.1:p.Val637=
XM_005266110.1:c.1826T= XP_005266167.1:p.Val609=
XM_006717288.2:c.1901T= XP_006717351.1:p.Val634=
XM_011519021.1:c.1928T= XP_011517323.1:p.Val643=
XM_011519022.1:c.1925T= XP_011517324.1:p.Val642=
XM_011519023.1:c.1907T= XP_011517325.1:p.Val636=
XM_011519024.1:c.1850T= XP_011517326.1:p.Val617=
XM_011519025.1:c.1826T= XP_011517327.1:p.Val609=
XM_011519026.1:c.1784T= XP_011517328.1:p.Val595=
XM_011519027.1:c.1928T= XP_011517329.1:p.Val643=
XM_011519028.1:c.1928T= XP_011517330.1:p.Val643=
XM_011519029.1:c.350T= XP_011517331.1:p.Val117=
XM_011519033.1:c.1763T= XP_011517335.1:p.Val588=
NM_001354259.1:c.1826T= NP_001341188.1:p.Val609=
NM_001354263.1:c.1898T= NP_001341192.1:p.Val633=
XM_005266105.5:c.1910T= XP_005266162.1:p.Val637=
XM_011519021.3:c.1928T= XP_011517323.1:p.Val643=
XM_011519022.3:c.1925T= XP_011517324.1:p.Val642=
XM_011519023.3:c.1907T= XP_011517325.1:p.Val636=
XM_011519029.3:c.350T= XP_011517331.1:p.Val117=
XM_017015134.1:c.1904T= XP_016870623.1:p.Val635=
XM_017015136.2:c.1820T= XP_016870625.1:p.Val607=
XM_017015137.1:c.1805T= XP_016870626.1:p.Val602=
XM_017015138.1:c.1805T= XP_016870627.1:p.Val602=
XM_024447674.1:c.1748T= XP_024303442.1:p.Val583=
XM_024447675.1:c.1682T= XP_024303443.1:p.Val561=
XM_024447676.1:c.1043T= XP_024303444.1:p.Val348=
XM_024447677.1:c.1043T= XP_024303445.1:p.Val348=
XM_024447678.1:c.1826T= XP_024303446.1:p.Val609=
XM_024447679.1:c.1826T= XP_024303447.1:p.Val609=
XM_024447680.1:c.1661T= XP_024303448.1:p.Val554=
NM_024757.5:c.1919T= MANE Select NP_079033.4:p.Val640=
NM_001145527.2:c.1919T= NP_001138999.1:p.Val640=
NM_001354259.2:c.1826T= NP_001341188.1:p.Val609=
NM_001354263.2:c.1898T= NP_001341192.1:p.Val633=