Canonical Allele Identifier: CA1884666544

Gene: EHMT1

Linked Data

• dbSNP Id: rs1950998968

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776858_137776877del , CM000671.2:g.137776858_137776877del	GRCh38
NC_000009.11:g.140671310_140671329del , CM000671.1:g.140671310_140671329del	GRCh37
NC_000009.10:g.139791131_139791150del	NCBI36
NG_011776.1:g.162867_162886del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2018+14_2018+33del MANE Select	ENSP00000417980.1:n.2018+14_2018+33del
ENST00000636027.1:c.1904+14_1904+33del	ENSP00000489961.1:n.1904+14_1904+33del
ENST00000637161.1:c.1925+14_1925+33del	ENSP00000490328.1:n.1925+14_1925+33del
ENST00000637261.1:c.2058+14_2058+33del	ENSP00000490815.1:n.2058+14_2058+33del
ENST00000638071.1:c.1645+14_1645+33del
ENST00000371394.6:c.*1753+14_*1753+33del	ENSP00000485945.1:n.*1753+14_*1753+33del
ENST00000460843.5:c.2018+14_2018+33del	ENSP00000417980.1:n.2018+14_2018+33del
ENST00000462484.5:c.2018+14_2018+33del	ENSP00000417328.1:n.2018+14_2018+33del
ENST00000462942.3:c.875+14_875+33del	ENSP00000436107.1:n.875+14_875+33del
ENST00000626603.1:n.1575_1594del
NM_001145527.1:c.2018+14_2018+33del	NP_001138999.1:n.2018+14_2018+33del
NM_024757.4:c.2018+14_2018+33del	NP_079033.4:n.2018+14_2018+33del
XM_005266105.3:c.2009+14_2009+33del	XP_005266162.1:n.2009+14_2009+33del
XM_005266110.1:c.1925+14_1925+33del	XP_005266167.1:n.1925+14_1925+33del
XM_006717288.2:c.2000+14_2000+33del	XP_006717351.1:n.2000+14_2000+33del
XM_011519021.1:c.2027+14_2027+33del	XP_011517323.1:n.2027+14_2027+33del
XM_011519022.1:c.2024+14_2024+33del	XP_011517324.1:n.2024+14_2024+33del
XM_011519023.1:c.2006+14_2006+33del	XP_011517325.1:n.2006+14_2006+33del
XM_011519024.1:c.1949+14_1949+33del	XP_011517326.1:n.1949+14_1949+33del
XM_011519025.1:c.1925+14_1925+33del	XP_011517327.1:n.1925+14_1925+33del
XM_011519026.1:c.1883+14_1883+33del	XP_011517328.1:n.1883+14_1883+33del
XM_011519027.1:c.2027+14_2027+33del	XP_011517329.1:n.2027+14_2027+33del
XM_011519028.1:c.2027+14_2027+33del	XP_011517330.1:n.2027+14_2027+33del
XM_011519029.1:c.449+14_449+33del	XP_011517331.1:n.449+14_449+33del
XM_011519033.1:c.1862+14_1862+33del	XP_011517335.1:n.1862+14_1862+33del
NM_001354259.1:c.1925+14_1925+33del	NP_001341188.1:n.1925+14_1925+33del
NM_001354263.1:c.1997+14_1997+33del	NP_001341192.1:n.1997+14_1997+33del
XM_005266105.5:c.2009+14_2009+33del	XP_005266162.1:n.2009+14_2009+33del
XM_011519021.3:c.2027+14_2027+33del	XP_011517323.1:n.2027+14_2027+33del
XM_011519022.3:c.2024+14_2024+33del	XP_011517324.1:n.2024+14_2024+33del
XM_011519023.3:c.2006+14_2006+33del	XP_011517325.1:n.2006+14_2006+33del
XM_011519029.3:c.449+14_449+33del	XP_011517331.1:n.449+14_449+33del
XM_017015134.1:c.2003+14_2003+33del	XP_016870623.1:n.2003+14_2003+33del
XM_017015136.2:c.1919+14_1919+33del	XP_016870625.1:n.1919+14_1919+33del
XM_017015137.1:c.1904+14_1904+33del	XP_016870626.1:n.1904+14_1904+33del
XM_017015138.1:c.1904+14_1904+33del	XP_016870627.1:n.1904+14_1904+33del
XM_024447674.1:c.1847+14_1847+33del	XP_024303442.1:n.1847+14_1847+33del
XM_024447675.1:c.1781+14_1781+33del	XP_024303443.1:n.1781+14_1781+33del
XM_024447676.1:c.1142+14_1142+33del	XP_024303444.1:n.1142+14_1142+33del
XM_024447677.1:c.1142+14_1142+33del	XP_024303445.1:n.1142+14_1142+33del
XM_024447678.1:c.1925+14_1925+33del	XP_024303446.1:n.1925+14_1925+33del
XM_024447679.1:c.1925+14_1925+33del	XP_024303447.1:n.1925+14_1925+33del
XM_024447680.1:c.1760+14_1760+33del	XP_024303448.1:n.1760+14_1760+33del
NM_024757.5:c.2018+14_2018+33del MANE Select	NP_079033.4:n.2018+14_2018+33del
NM_001145527.2:c.2018+14_2018+33del	NP_001138999.1:n.2018+14_2018+33del
NM_001354259.2:c.1925+14_1925+33del	NP_001341188.1:n.1925+14_1925+33del
NM_001354263.2:c.1997+14_1997+33del	NP_001341192.1:n.1997+14_1997+33del