Canonical Allele Identifier: CA2695211854

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776589_137776637del , CM000671.2:g.137776589_137776637del	GRCh38
NC_000009.11:g.140671041_140671089del , CM000671.1:g.140671041_140671089del	GRCh37
NC_000009.10:g.139790862_139790910del	NCBI36
NG_011776.1:g.162598_162646del

Transcript Alleles

HGVS	Amino-acid change
ENST00000460843.6:c.1792-29_1811del
ENST00000636027.1:c.1678-29_1697del
ENST00000637161.1:c.1699-29_1718del
ENST00000637261.1:c.1832-29_1851del
ENST00000638071.1:c.1419-29_1438del
ENST00000640639.1:c.961-29_980del
ENST00000371394.6:c.*1527-29_*1546del
ENST00000460843.5:c.1792-29_1811del
ENST00000462484.5:c.1792-29_1811del
ENST00000462942.3:c.649-29_668del
ENST00000465566.2:c.340-29_359del
ENST00000626603.1:n.1814_1862del
NM_001145527.1:c.1792-29_1811del
NM_024757.4:c.1792-29_1811del
XM_005266105.3:c.1783-29_1802del
XM_005266110.1:c.1699-29_1718del
XM_006717288.2:c.1774-29_1793del
XM_011519021.1:c.1801-29_1820del
XM_011519022.1:c.1798-29_1817del
XM_011519023.1:c.1780-29_1799del
XM_011519024.1:c.1723-29_1742del
XM_011519025.1:c.1699-29_1718del
XM_011519026.1:c.1657-29_1676del
XM_011519027.1:c.1801-29_1820del
XM_011519028.1:c.1801-29_1820del
XM_011519029.1:c.223-29_242del
XM_011519033.1:c.1636-29_1655del
NM_001354259.1:c.1699-29_1718del
NM_001354263.1:c.1771-29_1790del
XM_005266105.5:c.1783-29_1802del
XM_011519021.3:c.1801-29_1820del
XM_011519022.3:c.1798-29_1817del
XM_011519023.3:c.1780-29_1799del
XM_011519029.3:c.223-29_242del
XM_017015134.1:c.1777-29_1796del
XM_017015136.2:c.1693-29_1712del
XM_017015137.1:c.1678-29_1697del
XM_017015138.1:c.1678-29_1697del
XM_024447674.1:c.1621-29_1640del
XM_024447675.1:c.1555-29_1574del
XM_024447676.1:c.916-29_935del
XM_024447677.1:c.916-29_935del
XM_024447678.1:c.1699-29_1718del
XM_024447679.1:c.1699-29_1718del
XM_024447680.1:c.1534-29_1553del
NM_024757.5:c.1792-29_1811del
NM_001145527.2:c.1792-29_1811del
NM_001354259.2:c.1699-29_1718del
NM_001354263.2:c.1771-29_1790del