Canonical Allele Identifier: CA1130164451

Gene: EHMT1

Linked Data

• gnomAD v3: 9-137818495-A-AAGACTGTAGAGAGGCTGAGGGGGGGCGCCATGTACCGAGACTGTAGAGAGGCCGACTGAGGGGCGCCGTGTACCG
• gnomAD v4: 9-137818495-A-AAGACTGTAGAGAGGCTGAGGGGGGGCGCCATGTACCGAGACTGTAGAGAGGCCGACTGAGGGGCGCCGTGTACCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137818500_137818574dup , CM000671.2:g.137818500_137818574dup	GRCh38
NC_000009.11:g.140712952_140713026dup , CM000671.1:g.140712952_140713026dup	GRCh37
NC_000009.10:g.139832773_139832847dup	NCBI36
NG_011776.1:g.204509_204583dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3540+362_3540+436dup MANE Select	ENSP00000417980.1:n.3540+362_3540+436dup
ENST00000636526.1:n.26+362_26+436dup
ENST00000637161.1:c.3447+362_3447+436dup	ENSP00000490328.1:n.3447+362_3447+436dup
ENST00000637261.1:c.4114+362_4114+436dup	ENSP00000490815.1:n.4114+362_4114+436dup
ENST00000637748.1:n.521+362_521+436dup
ENST00000637891.1:c.1614+362_1614+436dup	ENSP00000490907.1:n.1614+362_1614+436dup
ENST00000460843.5:c.3540+362_3540+436dup	ENSP00000417980.1:n.3540+362_3540+436dup
ENST00000462942.3:c.2397+362_2397+436dup	ENSP00000436107.1:n.2397+362_2397+436dup
ENST00000475564.5:n.1264+362_1264+436dup
ENST00000494249.5:n.893+362_893+436dup
NM_024757.4:c.3540+362_3540+436dup	NP_079033.4:n.3540+362_3540+436dup
XM_005266105.3:c.3531+362_3531+436dup	XP_005266162.1:n.3531+362_3531+436dup
XM_005266110.1:c.3447+362_3447+436dup	XP_005266167.1:n.3447+362_3447+436dup
XM_006717288.2:c.3522+362_3522+436dup	XP_006717351.1:n.3522+362_3522+436dup
XM_011519021.1:c.3549+362_3549+436dup	XP_011517323.1:n.3549+362_3549+436dup
XM_011519022.1:c.3546+362_3546+436dup	XP_011517324.1:n.3546+362_3546+436dup
XM_011519023.1:c.3528+362_3528+436dup	XP_011517325.1:n.3528+362_3528+436dup
XM_011519024.1:c.3471+362_3471+436dup	XP_011517326.1:n.3471+362_3471+436dup
XM_011519025.1:c.3447+362_3447+436dup	XP_011517327.1:n.3447+362_3447+436dup
XM_011519026.1:c.3405+362_3405+436dup	XP_011517328.1:n.3405+362_3405+436dup
XM_011519029.1:c.1971+362_1971+436dup	XP_011517331.1:n.1971+362_1971+436dup
XM_011519030.1:c.1323+362_1323+436dup	XP_011517332.1:n.1323+362_1323+436dup
XM_011519031.1:c.1110+362_1110+436dup	XP_011517333.1:n.1110+362_1110+436dup
XM_011519032.1:c.1110+362_1110+436dup	XP_011517334.1:n.1110+362_1110+436dup
XM_011519033.1:c.3384+362_3384+436dup	XP_011517335.1:n.3384+362_3384+436dup
XR_930459.1:n.5297-4008_5297-3934dup
NM_001354263.1:c.3519+362_3519+436dup	NP_001341192.1:n.3519+362_3519+436dup
XM_005266105.5:c.3531+362_3531+436dup	XP_005266162.1:n.3531+362_3531+436dup
XM_011519021.3:c.3549+362_3549+436dup	XP_011517323.1:n.3549+362_3549+436dup
XM_011519022.3:c.3546+362_3546+436dup	XP_011517324.1:n.3546+362_3546+436dup
XM_011519023.3:c.3528+362_3528+436dup	XP_011517325.1:n.3528+362_3528+436dup
XM_011519029.3:c.1971+362_1971+436dup	XP_011517331.1:n.1971+362_1971+436dup
XM_011519030.3:c.1323+362_1323+436dup	XP_011517332.1:n.1323+362_1323+436dup
XM_017015134.1:c.3525+362_3525+436dup	XP_016870623.1:n.3525+362_3525+436dup
XM_017015136.2:c.3441+362_3441+436dup	XP_016870625.1:n.3441+362_3441+436dup
XM_017015137.1:c.3426+362_3426+436dup	XP_016870626.1:n.3426+362_3426+436dup
XM_017015138.1:c.3426+362_3426+436dup	XP_016870627.1:n.3426+362_3426+436dup
XM_024447674.1:c.3369+362_3369+436dup	XP_024303442.1:n.3369+362_3369+436dup
XM_024447675.1:c.3303+362_3303+436dup	XP_024303443.1:n.3303+362_3303+436dup
XM_024447676.1:c.2664+362_2664+436dup	XP_024303444.1:n.2664+362_2664+436dup
XM_024447677.1:c.2664+362_2664+436dup	XP_024303445.1:n.2664+362_2664+436dup
XM_024447680.1:c.3282+362_3282+436dup	XP_024303448.1:n.3282+362_3282+436dup
NM_024757.5:c.3540+362_3540+436dup MANE Select	NP_079033.4:n.3540+362_3540+436dup
NM_001354263.2:c.3519+362_3519+436dup	NP_001341192.1:n.3519+362_3519+436dup