Canonical Allele Identifier: CA2692890755
Gene: EHMT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137813318_137813319del , CM000671.2:g.137813318_137813319del GRCh38
NC_000009.11:g.140707770_140707771del , CM000671.1:g.140707770_140707771del GRCh37
NC_000009.10:g.139827591_139827592del NCBI36
NG_011776.1:g.199327_199328del

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.3036-68_3036-67del MANE Select ENSP00000417980.1:n.3036-68_3036-67del
ENST00000636027.1:c.2922-68_2922-67del ENSP00000489961.1:n.2922-68_2922-67del
ENST00000637161.1:c.2943-68_2943-67del ENSP00000490328.1:n.2943-68_2943-67del
ENST00000637261.1:c.3076-68_3076-67del ENSP00000490815.1:n.3076-68_3076-67del
ENST00000637891.1:c.930-68_930-67del ENSP00000490907.1:n.930-68_930-67del
ENST00000460843.5:c.3036-68_3036-67del ENSP00000417980.1:n.3036-68_3036-67del
ENST00000462942.3:c.1893-68_1893-67del ENSP00000436107.1:n.1893-68_1893-67del
ENST00000486164.5:c.723-68_723-67del
ENST00000488242.2:n.562-68_562-67del
NM_024757.4:c.3036-68_3036-67del NP_079033.4:n.3036-68_3036-67del
XM_005266105.3:c.3027-68_3027-67del XP_005266162.1:n.3027-68_3027-67del
XM_005266110.1:c.2943-68_2943-67del XP_005266167.1:n.2943-68_2943-67del
XM_006717288.2:c.3018-68_3018-67del XP_006717351.1:n.3018-68_3018-67del
XM_011519021.1:c.3045-68_3045-67del XP_011517323.1:n.3045-68_3045-67del
XM_011519022.1:c.3042-68_3042-67del XP_011517324.1:n.3042-68_3042-67del
XM_011519023.1:c.3024-68_3024-67del XP_011517325.1:n.3024-68_3024-67del
XM_011519024.1:c.2967-68_2967-67del XP_011517326.1:n.2967-68_2967-67del
XM_011519025.1:c.2943-68_2943-67del XP_011517327.1:n.2943-68_2943-67del
XM_011519026.1:c.2901-68_2901-67del XP_011517328.1:n.2901-68_2901-67del
XM_011519029.1:c.1467-68_1467-67del XP_011517331.1:n.1467-68_1467-67del
XM_011519030.1:c.819-68_819-67del XP_011517332.1:n.819-68_819-67del
XM_011519031.1:c.606-68_606-67del XP_011517333.1:n.606-68_606-67del
XM_011519032.1:c.606-68_606-67del XP_011517334.1:n.606-68_606-67del
XM_011519033.1:c.2880-68_2880-67del XP_011517335.1:n.2880-68_2880-67del
NM_001354263.1:c.3015-68_3015-67del NP_001341192.1:n.3015-68_3015-67del
XM_005266105.5:c.3027-68_3027-67del XP_005266162.1:n.3027-68_3027-67del
XM_011519021.3:c.3045-68_3045-67del XP_011517323.1:n.3045-68_3045-67del
XM_011519022.3:c.3042-68_3042-67del XP_011517324.1:n.3042-68_3042-67del
XM_011519023.3:c.3024-68_3024-67del XP_011517325.1:n.3024-68_3024-67del
XM_011519029.3:c.1467-68_1467-67del XP_011517331.1:n.1467-68_1467-67del
XM_011519030.3:c.819-68_819-67del XP_011517332.1:n.819-68_819-67del
XM_017015134.1:c.3021-68_3021-67del XP_016870623.1:n.3021-68_3021-67del
XM_017015136.2:c.2937-68_2937-67del XP_016870625.1:n.2937-68_2937-67del
XM_017015137.1:c.2922-68_2922-67del XP_016870626.1:n.2922-68_2922-67del
XM_017015138.1:c.2922-68_2922-67del XP_016870627.1:n.2922-68_2922-67del
XM_024447674.1:c.2865-68_2865-67del XP_024303442.1:n.2865-68_2865-67del
XM_024447675.1:c.2799-68_2799-67del XP_024303443.1:n.2799-68_2799-67del
XM_024447676.1:c.2160-68_2160-67del XP_024303444.1:n.2160-68_2160-67del
XM_024447677.1:c.2160-68_2160-67del XP_024303445.1:n.2160-68_2160-67del
XM_024447680.1:c.2778-68_2778-67del XP_024303448.1:n.2778-68_2778-67del
NM_024757.5:c.3036-68_3036-67del MANE Select NP_079033.4:n.3036-68_3036-67del
NM_001354263.2:c.3015-68_3015-67del NP_001341192.1:n.3015-68_3015-67del