Canonical Allele Identifier: CA2692883402

Gene: EHMT1

Linked Data

• gnomAD v4: 9-137776493-C-CCCGA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776496_137776499dup , CM000671.2:g.137776496_137776499dup	GRCh38
NC_000009.11:g.140670948_140670951dup , CM000671.1:g.140670948_140670951dup	GRCh37
NC_000009.10:g.139790769_139790772dup	NCBI36
NG_011776.1:g.162505_162508dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1792-122_1792-119dup MANE Select	ENSP00000417980.1:n.1792-122_1792-119dup
ENST00000636027.1:c.1678-122_1678-119dup	ENSP00000489961.1:n.1678-122_1678-119dup
ENST00000637161.1:c.1699-122_1699-119dup	ENSP00000490328.1:n.1699-122_1699-119dup
ENST00000637261.1:c.1832-122_1832-119dup	ENSP00000490815.1:n.1832-122_1832-119dup
ENST00000638071.1:c.1419-122_1419-119dup
ENST00000640639.1:c.961-122_961-119dup	ENSP00000491823.1:n.961-122_961-119dup
ENST00000371394.6:c.*1527-122_*1527-119dup	ENSP00000485945.1:n.*1527-122_*1527-119dup
ENST00000460843.5:c.1792-122_1792-119dup	ENSP00000417980.1:n.1792-122_1792-119dup
ENST00000462484.5:c.1792-122_1792-119dup	ENSP00000417328.1:n.1792-122_1792-119dup
ENST00000462942.3:c.649-122_649-119dup	ENSP00000436107.1:n.649-122_649-119dup
ENST00000465566.2:c.340-122_340-119dup	ENSP00000486261.1:n.340-122_340-119dup
NM_001145527.1:c.1792-122_1792-119dup	NP_001138999.1:n.1792-122_1792-119dup
NM_024757.4:c.1792-122_1792-119dup	NP_079033.4:n.1792-122_1792-119dup
XM_005266105.3:c.1783-122_1783-119dup	XP_005266162.1:n.1783-122_1783-119dup
XM_005266110.1:c.1699-122_1699-119dup	XP_005266167.1:n.1699-122_1699-119dup
XM_006717288.2:c.1774-122_1774-119dup	XP_006717351.1:n.1774-122_1774-119dup
XM_011519021.1:c.1801-122_1801-119dup	XP_011517323.1:n.1801-122_1801-119dup
XM_011519022.1:c.1798-122_1798-119dup	XP_011517324.1:n.1798-122_1798-119dup
XM_011519023.1:c.1780-122_1780-119dup	XP_011517325.1:n.1780-122_1780-119dup
XM_011519024.1:c.1723-122_1723-119dup	XP_011517326.1:n.1723-122_1723-119dup
XM_011519025.1:c.1699-122_1699-119dup	XP_011517327.1:n.1699-122_1699-119dup
XM_011519026.1:c.1657-122_1657-119dup	XP_011517328.1:n.1657-122_1657-119dup
XM_011519027.1:c.1801-122_1801-119dup	XP_011517329.1:n.1801-122_1801-119dup
XM_011519028.1:c.1801-122_1801-119dup	XP_011517330.1:n.1801-122_1801-119dup
XM_011519029.1:c.223-122_223-119dup	XP_011517331.1:n.223-122_223-119dup
XM_011519033.1:c.1636-122_1636-119dup	XP_011517335.1:n.1636-122_1636-119dup
NM_001354259.1:c.1699-122_1699-119dup	NP_001341188.1:n.1699-122_1699-119dup
NM_001354263.1:c.1771-122_1771-119dup	NP_001341192.1:n.1771-122_1771-119dup
XM_005266105.5:c.1783-122_1783-119dup	XP_005266162.1:n.1783-122_1783-119dup
XM_011519021.3:c.1801-122_1801-119dup	XP_011517323.1:n.1801-122_1801-119dup
XM_011519022.3:c.1798-122_1798-119dup	XP_011517324.1:n.1798-122_1798-119dup
XM_011519023.3:c.1780-122_1780-119dup	XP_011517325.1:n.1780-122_1780-119dup
XM_011519029.3:c.223-122_223-119dup	XP_011517331.1:n.223-122_223-119dup
XM_017015134.1:c.1777-122_1777-119dup	XP_016870623.1:n.1777-122_1777-119dup
XM_017015136.2:c.1693-122_1693-119dup	XP_016870625.1:n.1693-122_1693-119dup
XM_017015137.1:c.1678-122_1678-119dup	XP_016870626.1:n.1678-122_1678-119dup
XM_017015138.1:c.1678-122_1678-119dup	XP_016870627.1:n.1678-122_1678-119dup
XM_024447674.1:c.1621-122_1621-119dup	XP_024303442.1:n.1621-122_1621-119dup
XM_024447675.1:c.1555-122_1555-119dup	XP_024303443.1:n.1555-122_1555-119dup
XM_024447676.1:c.916-122_916-119dup	XP_024303444.1:n.916-122_916-119dup
XM_024447677.1:c.916-122_916-119dup	XP_024303445.1:n.916-122_916-119dup
XM_024447678.1:c.1699-122_1699-119dup	XP_024303446.1:n.1699-122_1699-119dup
XM_024447679.1:c.1699-122_1699-119dup	XP_024303447.1:n.1699-122_1699-119dup
XM_024447680.1:c.1534-122_1534-119dup	XP_024303448.1:n.1534-122_1534-119dup
NM_024757.5:c.1792-122_1792-119dup MANE Select	NP_079033.4:n.1792-122_1792-119dup
NM_001145527.2:c.1792-122_1792-119dup	NP_001138999.1:n.1792-122_1792-119dup
NM_001354259.2:c.1699-122_1699-119dup	NP_001341188.1:n.1699-122_1699-119dup
NM_001354263.2:c.1771-122_1771-119dup	NP_001341192.1:n.1771-122_1771-119dup