Canonical Allele Identifier: CA2841435991
Gene: EHMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137800833dup , CM000671.2:g.137800833dup GRCh38
NC_000009.11:g.140695285dup , CM000671.1:g.140695285dup GRCh37
NC_000009.10:g.139815106dup NCBI36
NG_011776.1:g.186842dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.2608-47dup MANE Select ENSP00000417980.1:n.2608-47dup
ENST00000636027.1:c.2494-47dup ENSP00000489961.1:n.2494-47dup
ENST00000637161.1:c.2515-47dup ENSP00000490328.1:n.2515-47dup
ENST00000637261.1:c.2648-47dup ENSP00000490815.1:n.2648-47dup
ENST00000637891.1:c.502-47dup ENSP00000490907.1:n.502-47dup
ENST00000637949.1:c.286-47dup ENSP00000489786.1:n.286-47dup
ENST00000460843.5:c.2608-47dup ENSP00000417980.1:n.2608-47dup
ENST00000462942.3:c.1465-47dup ENSP00000436107.1:n.1465-47dup
ENST00000482340.5:c.178-47dup ENSP00000486748.1:n.178-47dup
ENST00000486164.5:c.186-47dup
ENST00000488242.2:n.134-47dup
ENST00000493484.5:c.178-47dup ENSP00000486503.1:n.178-47dup
NM_024757.4:c.2608-47dup NP_079033.4:n.2608-47dup
XM_005266105.3:c.2599-47dup XP_005266162.1:n.2599-47dup
XM_005266110.1:c.2515-47dup XP_005266167.1:n.2515-47dup
XM_006717288.2:c.2590-47dup XP_006717351.1:n.2590-47dup
XM_011519021.1:c.2617-47dup XP_011517323.1:n.2617-47dup
XM_011519022.1:c.2614-47dup XP_011517324.1:n.2614-47dup
XM_011519023.1:c.2596-47dup XP_011517325.1:n.2596-47dup
XM_011519024.1:c.2539-47dup XP_011517326.1:n.2539-47dup
XM_011519025.1:c.2515-47dup XP_011517327.1:n.2515-47dup
XM_011519026.1:c.2473-47dup XP_011517328.1:n.2473-47dup
XM_011519027.1:c.2617-47dup XP_011517329.1:n.2617-47dup
XM_011519029.1:c.1039-47dup XP_011517331.1:n.1039-47dup
XM_011519030.1:c.391-47dup XP_011517332.1:n.391-47dup
XM_011519031.1:c.178-47dup XP_011517333.1:n.178-47dup
XM_011519032.1:c.178-47dup XP_011517334.1:n.178-47dup
XM_011519033.1:c.2452-47dup XP_011517335.1:n.2452-47dup
NM_001354263.1:c.2587-47dup NP_001341192.1:n.2587-47dup
XM_005266105.5:c.2599-47dup XP_005266162.1:n.2599-47dup
XM_011519021.3:c.2617-47dup XP_011517323.1:n.2617-47dup
XM_011519022.3:c.2614-47dup XP_011517324.1:n.2614-47dup
XM_011519023.3:c.2596-47dup XP_011517325.1:n.2596-47dup
XM_011519029.3:c.1039-47dup XP_011517331.1:n.1039-47dup
XM_011519030.3:c.391-47dup XP_011517332.1:n.391-47dup
XM_017015134.1:c.2593-47dup XP_016870623.1:n.2593-47dup
XM_017015136.2:c.2509-47dup XP_016870625.1:n.2509-47dup
XM_017015137.1:c.2494-47dup XP_016870626.1:n.2494-47dup
XM_017015138.1:c.2494-47dup XP_016870627.1:n.2494-47dup
XM_024447674.1:c.2437-47dup XP_024303442.1:n.2437-47dup
XM_024447675.1:c.2371-47dup XP_024303443.1:n.2371-47dup
XM_024447676.1:c.1732-47dup XP_024303444.1:n.1732-47dup
XM_024447677.1:c.1732-47dup XP_024303445.1:n.1732-47dup
XM_024447678.1:c.2515-47dup XP_024303446.1:n.2515-47dup
XM_024447680.1:c.2350-47dup XP_024303448.1:n.2350-47dup
NM_024757.5:c.2608-47dup MANE Select NP_079033.4:n.2608-47dup
NM_001354263.2:c.2587-47dup NP_001341192.1:n.2587-47dup