Canonical Allele Identifier: CA1884685809

Gene: EHMT1

Linked Data

• dbSNP Id: rs1954641946

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813286dup , CM000671.2:g.137813286dup	GRCh38
NC_000009.11:g.140707738dup , CM000671.1:g.140707738dup	GRCh37
NC_000009.10:g.139827559dup	NCBI36
NG_011776.1:g.199295dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3036-100dup MANE Select	ENSP00000417980.1:n.3036-100dup
ENST00000636027.1:c.2922-100dup	ENSP00000489961.1:n.2922-100dup
ENST00000637161.1:c.2943-100dup	ENSP00000490328.1:n.2943-100dup
ENST00000637261.1:c.3076-100dup	ENSP00000490815.1:n.3076-100dup
ENST00000637891.1:c.930-100dup	ENSP00000490907.1:n.930-100dup
ENST00000460843.5:c.3036-100dup	ENSP00000417980.1:n.3036-100dup
ENST00000462942.3:c.1893-100dup	ENSP00000436107.1:n.1893-100dup
ENST00000486164.5:c.723-100dup
ENST00000488242.2:n.562-100dup
NM_024757.4:c.3036-100dup	NP_079033.4:n.3036-100dup
XM_005266105.3:c.3027-100dup	XP_005266162.1:n.3027-100dup
XM_005266110.1:c.2943-100dup	XP_005266167.1:n.2943-100dup
XM_006717288.2:c.3018-100dup	XP_006717351.1:n.3018-100dup
XM_011519021.1:c.3045-100dup	XP_011517323.1:n.3045-100dup
XM_011519022.1:c.3042-100dup	XP_011517324.1:n.3042-100dup
XM_011519023.1:c.3024-100dup	XP_011517325.1:n.3024-100dup
XM_011519024.1:c.2967-100dup	XP_011517326.1:n.2967-100dup
XM_011519025.1:c.2943-100dup	XP_011517327.1:n.2943-100dup
XM_011519026.1:c.2901-100dup	XP_011517328.1:n.2901-100dup
XM_011519029.1:c.1467-100dup	XP_011517331.1:n.1467-100dup
XM_011519030.1:c.819-100dup	XP_011517332.1:n.819-100dup
XM_011519031.1:c.606-100dup	XP_011517333.1:n.606-100dup
XM_011519032.1:c.606-100dup	XP_011517334.1:n.606-100dup
XM_011519033.1:c.2880-100dup	XP_011517335.1:n.2880-100dup
NM_001354263.1:c.3015-100dup	NP_001341192.1:n.3015-100dup
XM_005266105.5:c.3027-100dup	XP_005266162.1:n.3027-100dup
XM_011519021.3:c.3045-100dup	XP_011517323.1:n.3045-100dup
XM_011519022.3:c.3042-100dup	XP_011517324.1:n.3042-100dup
XM_011519023.3:c.3024-100dup	XP_011517325.1:n.3024-100dup
XM_011519029.3:c.1467-100dup	XP_011517331.1:n.1467-100dup
XM_011519030.3:c.819-100dup	XP_011517332.1:n.819-100dup
XM_017015134.1:c.3021-100dup	XP_016870623.1:n.3021-100dup
XM_017015136.2:c.2937-100dup	XP_016870625.1:n.2937-100dup
XM_017015137.1:c.2922-100dup	XP_016870626.1:n.2922-100dup
XM_017015138.1:c.2922-100dup	XP_016870627.1:n.2922-100dup
XM_024447674.1:c.2865-100dup	XP_024303442.1:n.2865-100dup
XM_024447675.1:c.2799-100dup	XP_024303443.1:n.2799-100dup
XM_024447676.1:c.2160-100dup	XP_024303444.1:n.2160-100dup
XM_024447677.1:c.2160-100dup	XP_024303445.1:n.2160-100dup
XM_024447680.1:c.2778-100dup	XP_024303448.1:n.2778-100dup
NM_024757.5:c.3036-100dup MANE Select	NP_079033.4:n.3036-100dup
NM_001354263.2:c.3015-100dup	NP_001341192.1:n.3015-100dup