Canonical Allele Identifier: CA1884688558

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137818470_137818471delinsAG , CM000671.2:g.137818470_137818471delinsAG	GRCh38
NC_000009.11:g.140712922_140712923delinsAG , CM000671.1:g.140712922_140712923delinsAG	GRCh37
NC_000009.10:g.139832743_139832744delinsAG	NCBI36
NG_011776.1:g.204479_204480delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3540+332_3540+333delinsAG MANE Select	ENSP00000417980.1:n.3540+332_3540+333delinsAG
ENST00000636526.1:n.26+332_26+333delinsAG
ENST00000637161.1:c.3447+332_3447+333delinsAG	ENSP00000490328.1:n.3447+332_3447+333delinsAG
ENST00000637261.1:c.4114+332_4114+333delinsAG	ENSP00000490815.1:n.4114+332_4114+333delinsAG
ENST00000637748.1:n.521+332_521+333delinsAG
ENST00000637891.1:c.1614+332_1614+333delinsAG	ENSP00000490907.1:n.1614+332_1614+333delinsAG
ENST00000460843.5:c.3540+332_3540+333delinsAG	ENSP00000417980.1:n.3540+332_3540+333delinsAG
ENST00000462942.3:c.2397+332_2397+333delinsAG	ENSP00000436107.1:n.2397+332_2397+333delinsAG
ENST00000475564.5:n.1264+332_1264+333delinsAG
ENST00000494249.5:n.893+332_893+333delinsAG
NM_024757.4:c.3540+332_3540+333delinsAG	NP_079033.4:n.3540+332_3540+333delinsAG
XM_005266105.3:c.3531+332_3531+333delinsAG	XP_005266162.1:n.3531+332_3531+333delinsAG
XM_005266110.1:c.3447+332_3447+333delinsAG	XP_005266167.1:n.3447+332_3447+333delinsAG
XM_006717288.2:c.3522+332_3522+333delinsAG	XP_006717351.1:n.3522+332_3522+333delinsAG
XM_011519021.1:c.3549+332_3549+333delinsAG	XP_011517323.1:n.3549+332_3549+333delinsAG
XM_011519022.1:c.3546+332_3546+333delinsAG	XP_011517324.1:n.3546+332_3546+333delinsAG
XM_011519023.1:c.3528+332_3528+333delinsAG	XP_011517325.1:n.3528+332_3528+333delinsAG
XM_011519024.1:c.3471+332_3471+333delinsAG	XP_011517326.1:n.3471+332_3471+333delinsAG
XM_011519025.1:c.3447+332_3447+333delinsAG	XP_011517327.1:n.3447+332_3447+333delinsAG
XM_011519026.1:c.3405+332_3405+333delinsAG	XP_011517328.1:n.3405+332_3405+333delinsAG
XM_011519029.1:c.1971+332_1971+333delinsAG	XP_011517331.1:n.1971+332_1971+333delinsAG
XM_011519030.1:c.1323+332_1323+333delinsAG	XP_011517332.1:n.1323+332_1323+333delinsAG
XM_011519031.1:c.1110+332_1110+333delinsAG	XP_011517333.1:n.1110+332_1110+333delinsAG
XM_011519032.1:c.1110+332_1110+333delinsAG	XP_011517334.1:n.1110+332_1110+333delinsAG
XM_011519033.1:c.3384+332_3384+333delinsAG	XP_011517335.1:n.3384+332_3384+333delinsAG
XR_930459.1:n.5297-3909_5297-3908delinsCT
NM_001354263.1:c.3519+332_3519+333delinsAG	NP_001341192.1:n.3519+332_3519+333delinsAG
XM_005266105.5:c.3531+332_3531+333delinsAG	XP_005266162.1:n.3531+332_3531+333delinsAG
XM_011519021.3:c.3549+332_3549+333delinsAG	XP_011517323.1:n.3549+332_3549+333delinsAG
XM_011519022.3:c.3546+332_3546+333delinsAG	XP_011517324.1:n.3546+332_3546+333delinsAG
XM_011519023.3:c.3528+332_3528+333delinsAG	XP_011517325.1:n.3528+332_3528+333delinsAG
XM_011519029.3:c.1971+332_1971+333delinsAG	XP_011517331.1:n.1971+332_1971+333delinsAG
XM_011519030.3:c.1323+332_1323+333delinsAG	XP_011517332.1:n.1323+332_1323+333delinsAG
XM_017015134.1:c.3525+332_3525+333delinsAG	XP_016870623.1:n.3525+332_3525+333delinsAG
XM_017015136.2:c.3441+332_3441+333delinsAG	XP_016870625.1:n.3441+332_3441+333delinsAG
XM_017015137.1:c.3426+332_3426+333delinsAG	XP_016870626.1:n.3426+332_3426+333delinsAG
XM_017015138.1:c.3426+332_3426+333delinsAG	XP_016870627.1:n.3426+332_3426+333delinsAG
XM_024447674.1:c.3369+332_3369+333delinsAG	XP_024303442.1:n.3369+332_3369+333delinsAG
XM_024447675.1:c.3303+332_3303+333delinsAG	XP_024303443.1:n.3303+332_3303+333delinsAG
XM_024447676.1:c.2664+332_2664+333delinsAG	XP_024303444.1:n.2664+332_2664+333delinsAG
XM_024447677.1:c.2664+332_2664+333delinsAG	XP_024303445.1:n.2664+332_2664+333delinsAG
XM_024447680.1:c.3282+332_3282+333delinsAG	XP_024303448.1:n.3282+332_3282+333delinsAG
NM_024757.5:c.3540+332_3540+333delinsAG MANE Select	NP_079033.4:n.3540+332_3540+333delinsAG
NM_001354263.2:c.3519+332_3519+333delinsAG	NP_001341192.1:n.3519+332_3519+333delinsAG