Canonical Allele Identifier: CA2692883567

Gene: EHMT1

Linked Data

• gnomAD v4: 9-137776988-GAC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776989_137776990del , CM000671.2:g.137776989_137776990del	GRCh38
NC_000009.11:g.140671441_140671442del , CM000671.1:g.140671441_140671442del	GRCh37
NC_000009.10:g.139791262_139791263del	NCBI36
NG_011776.1:g.162998_162999del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2018+145_2018+146del MANE Select	ENSP00000417980.1:n.2018+145_2018+146del
ENST00000636027.1:c.1904+145_1904+146del	ENSP00000489961.1:n.1904+145_1904+146del
ENST00000637161.1:c.1925+145_1925+146del	ENSP00000490328.1:n.1925+145_1925+146del
ENST00000637261.1:c.2058+145_2058+146del	ENSP00000490815.1:n.2058+145_2058+146del
ENST00000638071.1:c.1645+145_1645+146del
ENST00000371394.6:c.*1753+145_*1753+146del	ENSP00000485945.1:n.*1753+145_*1753+146del
ENST00000460843.5:c.2018+145_2018+146del	ENSP00000417980.1:n.2018+145_2018+146del
ENST00000462484.5:c.2018+145_2018+146del	ENSP00000417328.1:n.2018+145_2018+146del
ENST00000462942.3:c.875+145_875+146del	ENSP00000436107.1:n.875+145_875+146del
ENST00000626603.1:n.1459_1460del
NM_001145527.1:c.2018+145_2018+146del	NP_001138999.1:n.2018+145_2018+146del
NM_024757.4:c.2018+145_2018+146del	NP_079033.4:n.2018+145_2018+146del
XM_005266105.3:c.2009+145_2009+146del	XP_005266162.1:n.2009+145_2009+146del
XM_005266110.1:c.1925+145_1925+146del	XP_005266167.1:n.1925+145_1925+146del
XM_006717288.2:c.2000+145_2000+146del	XP_006717351.1:n.2000+145_2000+146del
XM_011519021.1:c.2027+145_2027+146del	XP_011517323.1:n.2027+145_2027+146del
XM_011519022.1:c.2024+145_2024+146del	XP_011517324.1:n.2024+145_2024+146del
XM_011519023.1:c.2006+145_2006+146del	XP_011517325.1:n.2006+145_2006+146del
XM_011519024.1:c.1949+145_1949+146del	XP_011517326.1:n.1949+145_1949+146del
XM_011519025.1:c.1925+145_1925+146del	XP_011517327.1:n.1925+145_1925+146del
XM_011519026.1:c.1883+145_1883+146del	XP_011517328.1:n.1883+145_1883+146del
XM_011519027.1:c.2027+145_2027+146del	XP_011517329.1:n.2027+145_2027+146del
XM_011519028.1:c.2027+145_2027+146del	XP_011517330.1:n.2027+145_2027+146del
XM_011519029.1:c.449+145_449+146del	XP_011517331.1:n.449+145_449+146del
XM_011519033.1:c.1862+145_1862+146del	XP_011517335.1:n.1862+145_1862+146del
NM_001354259.1:c.1925+145_1925+146del	NP_001341188.1:n.1925+145_1925+146del
NM_001354263.1:c.1997+145_1997+146del	NP_001341192.1:n.1997+145_1997+146del
XM_005266105.5:c.2009+145_2009+146del	XP_005266162.1:n.2009+145_2009+146del
XM_011519021.3:c.2027+145_2027+146del	XP_011517323.1:n.2027+145_2027+146del
XM_011519022.3:c.2024+145_2024+146del	XP_011517324.1:n.2024+145_2024+146del
XM_011519023.3:c.2006+145_2006+146del	XP_011517325.1:n.2006+145_2006+146del
XM_011519029.3:c.449+145_449+146del	XP_011517331.1:n.449+145_449+146del
XM_017015134.1:c.2003+145_2003+146del	XP_016870623.1:n.2003+145_2003+146del
XM_017015136.2:c.1919+145_1919+146del	XP_016870625.1:n.1919+145_1919+146del
XM_017015137.1:c.1904+145_1904+146del	XP_016870626.1:n.1904+145_1904+146del
XM_017015138.1:c.1904+145_1904+146del	XP_016870627.1:n.1904+145_1904+146del
XM_024447674.1:c.1847+145_1847+146del	XP_024303442.1:n.1847+145_1847+146del
XM_024447675.1:c.1781+145_1781+146del	XP_024303443.1:n.1781+145_1781+146del
XM_024447676.1:c.1142+145_1142+146del	XP_024303444.1:n.1142+145_1142+146del
XM_024447677.1:c.1142+145_1142+146del	XP_024303445.1:n.1142+145_1142+146del
XM_024447678.1:c.1925+145_1925+146del	XP_024303446.1:n.1925+145_1925+146del
XM_024447679.1:c.1925+145_1925+146del	XP_024303447.1:n.1925+145_1925+146del
XM_024447680.1:c.1760+145_1760+146del	XP_024303448.1:n.1760+145_1760+146del
NM_024757.5:c.2018+145_2018+146del MANE Select	NP_079033.4:n.2018+145_2018+146del
NM_001145527.2:c.2018+145_2018+146del	NP_001138999.1:n.2018+145_2018+146del
NM_001354259.2:c.1925+145_1925+146del	NP_001341188.1:n.1925+145_1925+146del
NM_001354263.2:c.1997+145_1997+146del	NP_001341192.1:n.1997+145_1997+146del