Canonical Allele Identifier: CA1884684987
Gene: EHMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137811618G= , CM000671.2:g.137811618G= GRCh38
NC_000009.11:g.140706070G= , CM000671.1:g.140706070G= GRCh37
NC_000009.10:g.139825891G= NCBI36
NG_011776.1:g.197627G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.2867+3G= MANE Select ENSP00000417980.1:n.2867+3G=
ENST00000636027.1:c.2753+3G= ENSP00000489961.1:n.2753+3G=
ENST00000637161.1:c.2774+3G= ENSP00000490328.1:n.2774+3G=
ENST00000637261.1:c.2907+3G= ENSP00000490815.1:n.2907+3G=
ENST00000637891.1:c.761+3G= ENSP00000490907.1:n.761+3G=
ENST00000460843.5:c.2867+3G= ENSP00000417980.1:n.2867+3G=
ENST00000462942.3:c.1724+3G= ENSP00000436107.1:n.1724+3G=
ENST00000486164.5:c.554+3G=
ENST00000488242.2:n.393+3G=
NM_024757.4:c.2867+3G= NP_079033.4:n.2867+3G=
XM_005266105.3:c.2858+3G= XP_005266162.1:n.2858+3G=
XM_005266110.1:c.2774+3G= XP_005266167.1:n.2774+3G=
XM_006717288.2:c.2849+3G= XP_006717351.1:n.2849+3G=
XM_011519021.1:c.2876+3G= XP_011517323.1:n.2876+3G=
XM_011519022.1:c.2873+3G= XP_011517324.1:n.2873+3G=
XM_011519023.1:c.2855+3G= XP_011517325.1:n.2855+3G=
XM_011519024.1:c.2798+3G= XP_011517326.1:n.2798+3G=
XM_011519025.1:c.2774+3G= XP_011517327.1:n.2774+3G=
XM_011519026.1:c.2732+3G= XP_011517328.1:n.2732+3G=
XM_011519029.1:c.1298+3G= XP_011517331.1:n.1298+3G=
XM_011519030.1:c.650+3G= XP_011517332.1:n.650+3G=
XM_011519031.1:c.437+3G= XP_011517333.1:n.437+3G=
XM_011519032.1:c.437+3G= XP_011517334.1:n.437+3G=
XM_011519033.1:c.2711+3G= XP_011517335.1:n.2711+3G=
NM_001354263.1:c.2846+3G= NP_001341192.1:n.2846+3G=
XM_005266105.5:c.2858+3G= XP_005266162.1:n.2858+3G=
XM_011519021.3:c.2876+3G= XP_011517323.1:n.2876+3G=
XM_011519022.3:c.2873+3G= XP_011517324.1:n.2873+3G=
XM_011519023.3:c.2855+3G= XP_011517325.1:n.2855+3G=
XM_011519029.3:c.1298+3G= XP_011517331.1:n.1298+3G=
XM_011519030.3:c.650+3G= XP_011517332.1:n.650+3G=
XM_017015134.1:c.2852+3G= XP_016870623.1:n.2852+3G=
XM_017015136.2:c.2768+3G= XP_016870625.1:n.2768+3G=
XM_017015137.1:c.2753+3G= XP_016870626.1:n.2753+3G=
XM_017015138.1:c.2753+3G= XP_016870627.1:n.2753+3G=
XM_024447674.1:c.2696+3G= XP_024303442.1:n.2696+3G=
XM_024447675.1:c.2630+3G= XP_024303443.1:n.2630+3G=
XM_024447676.1:c.1991+3G= XP_024303444.1:n.1991+3G=
XM_024447677.1:c.1991+3G= XP_024303445.1:n.1991+3G=
XM_024447680.1:c.2609+3G= XP_024303448.1:n.2609+3G=
NM_024757.5:c.2867+3G= MANE Select NP_079033.4:n.2867+3G=
NM_001354263.2:c.2846+3G= NP_001341192.1:n.2846+3G=