Canonical Allele Identifier: CA2786319607

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813208_137813212del , CM000671.2:g.137813208_137813212del	GRCh38
NC_000009.11:g.140707660_140707664del , CM000671.1:g.140707660_140707664del	GRCh37
NC_000009.10:g.139827481_139827485del	NCBI36
NG_011776.1:g.199217_199221del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3035+35_3035+39del MANE Select	ENSP00000417980.1:n.3035+35_3035+39del
ENST00000636027.1:c.2921+35_2921+39del	ENSP00000489961.1:n.2921+35_2921+39del
ENST00000637161.1:c.2942+35_2942+39del	ENSP00000490328.1:n.2942+35_2942+39del
ENST00000637261.1:c.3075+35_3075+39del	ENSP00000490815.1:n.3075+35_3075+39del
ENST00000637891.1:c.929+35_929+39del	ENSP00000490907.1:n.929+35_929+39del
ENST00000460843.5:c.3035+35_3035+39del	ENSP00000417980.1:n.3035+35_3035+39del
ENST00000462942.3:c.1892+35_1892+39del	ENSP00000436107.1:n.1892+35_1892+39del
ENST00000486164.5:c.722+35_722+39del
ENST00000488242.2:n.561+35_561+39del
NM_024757.4:c.3035+35_3035+39del	NP_079033.4:n.3035+35_3035+39del
XM_005266105.3:c.3026+35_3026+39del	XP_005266162.1:n.3026+35_3026+39del
XM_005266110.1:c.2942+35_2942+39del	XP_005266167.1:n.2942+35_2942+39del
XM_006717288.2:c.3017+35_3017+39del	XP_006717351.1:n.3017+35_3017+39del
XM_011519021.1:c.3044+35_3044+39del	XP_011517323.1:n.3044+35_3044+39del
XM_011519022.1:c.3041+35_3041+39del	XP_011517324.1:n.3041+35_3041+39del
XM_011519023.1:c.3023+35_3023+39del	XP_011517325.1:n.3023+35_3023+39del
XM_011519024.1:c.2966+35_2966+39del	XP_011517326.1:n.2966+35_2966+39del
XM_011519025.1:c.2942+35_2942+39del	XP_011517327.1:n.2942+35_2942+39del
XM_011519026.1:c.2900+35_2900+39del	XP_011517328.1:n.2900+35_2900+39del
XM_011519029.1:c.1466+35_1466+39del	XP_011517331.1:n.1466+35_1466+39del
XM_011519030.1:c.818+35_818+39del	XP_011517332.1:n.818+35_818+39del
XM_011519031.1:c.605+35_605+39del	XP_011517333.1:n.605+35_605+39del
XM_011519032.1:c.605+35_605+39del	XP_011517334.1:n.605+35_605+39del
XM_011519033.1:c.2879+35_2879+39del	XP_011517335.1:n.2879+35_2879+39del
NM_001354263.1:c.3014+35_3014+39del	NP_001341192.1:n.3014+35_3014+39del
XM_005266105.5:c.3026+35_3026+39del	XP_005266162.1:n.3026+35_3026+39del
XM_011519021.3:c.3044+35_3044+39del	XP_011517323.1:n.3044+35_3044+39del
XM_011519022.3:c.3041+35_3041+39del	XP_011517324.1:n.3041+35_3041+39del
XM_011519023.3:c.3023+35_3023+39del	XP_011517325.1:n.3023+35_3023+39del
XM_011519029.3:c.1466+35_1466+39del	XP_011517331.1:n.1466+35_1466+39del
XM_011519030.3:c.818+35_818+39del	XP_011517332.1:n.818+35_818+39del
XM_017015134.1:c.3020+35_3020+39del	XP_016870623.1:n.3020+35_3020+39del
XM_017015136.2:c.2936+35_2936+39del	XP_016870625.1:n.2936+35_2936+39del
XM_017015137.1:c.2921+35_2921+39del	XP_016870626.1:n.2921+35_2921+39del
XM_017015138.1:c.2921+35_2921+39del	XP_016870627.1:n.2921+35_2921+39del
XM_024447674.1:c.2864+35_2864+39del	XP_024303442.1:n.2864+35_2864+39del
XM_024447675.1:c.2798+35_2798+39del	XP_024303443.1:n.2798+35_2798+39del
XM_024447676.1:c.2159+35_2159+39del	XP_024303444.1:n.2159+35_2159+39del
XM_024447677.1:c.2159+35_2159+39del	XP_024303445.1:n.2159+35_2159+39del
XM_024447680.1:c.2777+35_2777+39del	XP_024303448.1:n.2777+35_2777+39del
NM_024757.5:c.3035+35_3035+39del MANE Select	NP_079033.4:n.3035+35_3035+39del
NM_001354263.2:c.3014+35_3014+39del	NP_001341192.1:n.3014+35_3014+39del