Canonical Allele Identifier: CA2692895093

Gene: EHMT1

Linked Data

• gnomAD v4: 9-137818293-CCTTGGTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137818296_137818302del , CM000671.2:g.137818296_137818302del	GRCh38
NC_000009.11:g.140712748_140712754del , CM000671.1:g.140712748_140712754del	GRCh37
NC_000009.10:g.139832569_139832575del	NCBI36
NG_011776.1:g.204305_204311del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3540+158_3540+164del MANE Select	ENSP00000417980.1:n.3540+158_3540+164del
ENST00000636526.1:n.26+158_26+164del
ENST00000637161.1:c.3447+158_3447+164del	ENSP00000490328.1:n.3447+158_3447+164del
ENST00000637261.1:c.4114+158_4114+164del	ENSP00000490815.1:n.4114+158_4114+164del
ENST00000637748.1:n.521+158_521+164del
ENST00000637891.1:c.1614+158_1614+164del	ENSP00000490907.1:n.1614+158_1614+164del
ENST00000460843.5:c.3540+158_3540+164del	ENSP00000417980.1:n.3540+158_3540+164del
ENST00000462942.3:c.2397+158_2397+164del	ENSP00000436107.1:n.2397+158_2397+164del
ENST00000475564.5:n.1264+158_1264+164del
ENST00000494249.5:n.893+158_893+164del
NM_024757.4:c.3540+158_3540+164del	NP_079033.4:n.3540+158_3540+164del
XM_005266105.3:c.3531+158_3531+164del	XP_005266162.1:n.3531+158_3531+164del
XM_005266110.1:c.3447+158_3447+164del	XP_005266167.1:n.3447+158_3447+164del
XM_006717288.2:c.3522+158_3522+164del	XP_006717351.1:n.3522+158_3522+164del
XM_011519021.1:c.3549+158_3549+164del	XP_011517323.1:n.3549+158_3549+164del
XM_011519022.1:c.3546+158_3546+164del	XP_011517324.1:n.3546+158_3546+164del
XM_011519023.1:c.3528+158_3528+164del	XP_011517325.1:n.3528+158_3528+164del
XM_011519024.1:c.3471+158_3471+164del	XP_011517326.1:n.3471+158_3471+164del
XM_011519025.1:c.3447+158_3447+164del	XP_011517327.1:n.3447+158_3447+164del
XM_011519026.1:c.3405+158_3405+164del	XP_011517328.1:n.3405+158_3405+164del
XM_011519029.1:c.1971+158_1971+164del	XP_011517331.1:n.1971+158_1971+164del
XM_011519030.1:c.1323+158_1323+164del	XP_011517332.1:n.1323+158_1323+164del
XM_011519031.1:c.1110+158_1110+164del	XP_011517333.1:n.1110+158_1110+164del
XM_011519032.1:c.1110+158_1110+164del	XP_011517334.1:n.1110+158_1110+164del
XM_011519033.1:c.3384+158_3384+164del	XP_011517335.1:n.3384+158_3384+164del
XR_930459.1:n.5297-3738_5297-3732del
NM_001354263.1:c.3519+158_3519+164del	NP_001341192.1:n.3519+158_3519+164del
XM_005266105.5:c.3531+158_3531+164del	XP_005266162.1:n.3531+158_3531+164del
XM_011519021.3:c.3549+158_3549+164del	XP_011517323.1:n.3549+158_3549+164del
XM_011519022.3:c.3546+158_3546+164del	XP_011517324.1:n.3546+158_3546+164del
XM_011519023.3:c.3528+158_3528+164del	XP_011517325.1:n.3528+158_3528+164del
XM_011519029.3:c.1971+158_1971+164del	XP_011517331.1:n.1971+158_1971+164del
XM_011519030.3:c.1323+158_1323+164del	XP_011517332.1:n.1323+158_1323+164del
XM_017015134.1:c.3525+158_3525+164del	XP_016870623.1:n.3525+158_3525+164del
XM_017015136.2:c.3441+158_3441+164del	XP_016870625.1:n.3441+158_3441+164del
XM_017015137.1:c.3426+158_3426+164del	XP_016870626.1:n.3426+158_3426+164del
XM_017015138.1:c.3426+158_3426+164del	XP_016870627.1:n.3426+158_3426+164del
XM_024447674.1:c.3369+158_3369+164del	XP_024303442.1:n.3369+158_3369+164del
XM_024447675.1:c.3303+158_3303+164del	XP_024303443.1:n.3303+158_3303+164del
XM_024447676.1:c.2664+158_2664+164del	XP_024303444.1:n.2664+158_2664+164del
XM_024447677.1:c.2664+158_2664+164del	XP_024303445.1:n.2664+158_2664+164del
XM_024447680.1:c.3282+158_3282+164del	XP_024303448.1:n.3282+158_3282+164del
NM_024757.5:c.3540+158_3540+164del MANE Select	NP_079033.4:n.3540+158_3540+164del
NM_001354263.2:c.3519+158_3519+164del	NP_001341192.1:n.3519+158_3519+164del