Canonical Allele Identifier: CA1884688554

Gene: EHMT1

Linked Data

• dbSNP Id: rs1955105253

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137818467_137818468del , CM000671.2:g.137818467_137818468del	GRCh38
NC_000009.11:g.140712919_140712920del , CM000671.1:g.140712919_140712920del	GRCh37
NC_000009.10:g.139832740_139832741del	NCBI36
NG_011776.1:g.204476_204477del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3540+329_3540+330del MANE Select	ENSP00000417980.1:n.3540+329_3540+330del
ENST00000636526.1:n.26+329_26+330del
ENST00000637161.1:c.3447+329_3447+330del	ENSP00000490328.1:n.3447+329_3447+330del
ENST00000637261.1:c.4114+329_4114+330del	ENSP00000490815.1:n.4114+329_4114+330del
ENST00000637748.1:n.521+329_521+330del
ENST00000637891.1:c.1614+329_1614+330del	ENSP00000490907.1:n.1614+329_1614+330del
ENST00000460843.5:c.3540+329_3540+330del	ENSP00000417980.1:n.3540+329_3540+330del
ENST00000462942.3:c.2397+329_2397+330del	ENSP00000436107.1:n.2397+329_2397+330del
ENST00000475564.5:n.1264+329_1264+330del
ENST00000494249.5:n.893+329_893+330del
NM_024757.4:c.3540+329_3540+330del	NP_079033.4:n.3540+329_3540+330del
XM_005266105.3:c.3531+329_3531+330del	XP_005266162.1:n.3531+329_3531+330del
XM_005266110.1:c.3447+329_3447+330del	XP_005266167.1:n.3447+329_3447+330del
XM_006717288.2:c.3522+329_3522+330del	XP_006717351.1:n.3522+329_3522+330del
XM_011519021.1:c.3549+329_3549+330del	XP_011517323.1:n.3549+329_3549+330del
XM_011519022.1:c.3546+329_3546+330del	XP_011517324.1:n.3546+329_3546+330del
XM_011519023.1:c.3528+329_3528+330del	XP_011517325.1:n.3528+329_3528+330del
XM_011519024.1:c.3471+329_3471+330del	XP_011517326.1:n.3471+329_3471+330del
XM_011519025.1:c.3447+329_3447+330del	XP_011517327.1:n.3447+329_3447+330del
XM_011519026.1:c.3405+329_3405+330del	XP_011517328.1:n.3405+329_3405+330del
XM_011519029.1:c.1971+329_1971+330del	XP_011517331.1:n.1971+329_1971+330del
XM_011519030.1:c.1323+329_1323+330del	XP_011517332.1:n.1323+329_1323+330del
XM_011519031.1:c.1110+329_1110+330del	XP_011517333.1:n.1110+329_1110+330del
XM_011519032.1:c.1110+329_1110+330del	XP_011517334.1:n.1110+329_1110+330del
XM_011519033.1:c.3384+329_3384+330del	XP_011517335.1:n.3384+329_3384+330del
XR_930459.1:n.5297-3904_5297-3903del
NM_001354263.1:c.3519+329_3519+330del	NP_001341192.1:n.3519+329_3519+330del
XM_005266105.5:c.3531+329_3531+330del	XP_005266162.1:n.3531+329_3531+330del
XM_011519021.3:c.3549+329_3549+330del	XP_011517323.1:n.3549+329_3549+330del
XM_011519022.3:c.3546+329_3546+330del	XP_011517324.1:n.3546+329_3546+330del
XM_011519023.3:c.3528+329_3528+330del	XP_011517325.1:n.3528+329_3528+330del
XM_011519029.3:c.1971+329_1971+330del	XP_011517331.1:n.1971+329_1971+330del
XM_011519030.3:c.1323+329_1323+330del	XP_011517332.1:n.1323+329_1323+330del
XM_017015134.1:c.3525+329_3525+330del	XP_016870623.1:n.3525+329_3525+330del
XM_017015136.2:c.3441+329_3441+330del	XP_016870625.1:n.3441+329_3441+330del
XM_017015137.1:c.3426+329_3426+330del	XP_016870626.1:n.3426+329_3426+330del
XM_017015138.1:c.3426+329_3426+330del	XP_016870627.1:n.3426+329_3426+330del
XM_024447674.1:c.3369+329_3369+330del	XP_024303442.1:n.3369+329_3369+330del
XM_024447675.1:c.3303+329_3303+330del	XP_024303443.1:n.3303+329_3303+330del
XM_024447676.1:c.2664+329_2664+330del	XP_024303444.1:n.2664+329_2664+330del
XM_024447677.1:c.2664+329_2664+330del	XP_024303445.1:n.2664+329_2664+330del
XM_024447680.1:c.3282+329_3282+330del	XP_024303448.1:n.3282+329_3282+330del
NM_024757.5:c.3540+329_3540+330del MANE Select	NP_079033.4:n.3540+329_3540+330del
NM_001354263.2:c.3519+329_3519+330del	NP_001341192.1:n.3519+329_3519+330del