Canonical Allele Identifier: CA375775419

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671071G>C (hg19) ; chr9:g.137776619G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776619G>C , CM000671.2:g.137776619G>C	GRCh38
NC_000009.11:g.140671071G>C , CM000671.1:g.140671071G>C	GRCh37
NC_000009.10:g.139790892G>C	NCBI36
NG_011776.1:g.162628G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1793G>C MANE Select	ENSP00000417980.1:p.Gly598Ala
ENST00000636027.1:c.1679G>C	ENSP00000489961.1:p.Gly560Ala
ENST00000637161.1:c.1700G>C	ENSP00000490328.1:p.Gly567Ala
ENST00000637261.1:c.1833G>C	ENSP00000490815.1:n.1833G>C
ENST00000638071.1:c.1420G>C
ENST00000640639.1:c.962G>C	ENSP00000491823.1:p.Gly321Ala
ENST00000371394.6:c.*1528G>C	ENSP00000485945.1:n.*1528G>C
ENST00000460843.5:c.1793G>C	ENSP00000417980.1:p.Gly598Ala
ENST00000462484.5:c.1793G>C	ENSP00000417328.1:p.Gly598Ala
ENST00000462942.3:c.650G>C	ENSP00000436107.1:p.Gly217Ala
ENST00000465566.2:c.341G>C	ENSP00000486261.1:p.Gly114Ala
ENST00000626603.1:n.1830C>G
NM_001145527.1:c.1793G>C	NP_001138999.1:p.Gly598Ala
NM_024757.4:c.1793G>C	NP_079033.4:p.Gly598Ala
XM_005266105.3:c.1784G>C	XP_005266162.1:p.Gly595Ala
XM_005266110.1:c.1700G>C	XP_005266167.1:p.Gly567Ala
XM_006717288.2:c.1775G>C	XP_006717351.1:p.Gly592Ala
XM_011519021.1:c.1802G>C	XP_011517323.1:p.Gly601Ala
XM_011519022.1:c.1799G>C	XP_011517324.1:p.Gly600Ala
XM_011519023.1:c.1781G>C	XP_011517325.1:p.Gly594Ala
XM_011519024.1:c.1724G>C	XP_011517326.1:p.Gly575Ala
XM_011519025.1:c.1700G>C	XP_011517327.1:p.Gly567Ala
XM_011519026.1:c.1658G>C	XP_011517328.1:p.Gly553Ala
XM_011519027.1:c.1802G>C	XP_011517329.1:p.Gly601Ala
XM_011519028.1:c.1802G>C	XP_011517330.1:p.Gly601Ala
XM_011519029.1:c.224G>C	XP_011517331.1:p.Gly75Ala
XM_011519033.1:c.1637G>C	XP_011517335.1:p.Gly546Ala
NM_001354259.1:c.1700G>C	NP_001341188.1:p.Gly567Ala
NM_001354263.1:c.1772G>C	NP_001341192.1:p.Gly591Ala
XM_005266105.5:c.1784G>C	XP_005266162.1:p.Gly595Ala
XM_011519021.3:c.1802G>C	XP_011517323.1:p.Gly601Ala
XM_011519022.3:c.1799G>C	XP_011517324.1:p.Gly600Ala
XM_011519023.3:c.1781G>C	XP_011517325.1:p.Gly594Ala
XM_011519029.3:c.224G>C	XP_011517331.1:p.Gly75Ala
XM_017015134.1:c.1778G>C	XP_016870623.1:p.Gly593Ala
XM_017015136.2:c.1694G>C	XP_016870625.1:p.Gly565Ala
XM_017015137.1:c.1679G>C	XP_016870626.1:p.Gly560Ala
XM_017015138.1:c.1679G>C	XP_016870627.1:p.Gly560Ala
XM_024447674.1:c.1622G>C	XP_024303442.1:p.Gly541Ala
XM_024447675.1:c.1556G>C	XP_024303443.1:p.Gly519Ala
XM_024447676.1:c.917G>C	XP_024303444.1:p.Gly306Ala
XM_024447677.1:c.917G>C	XP_024303445.1:p.Gly306Ala
XM_024447678.1:c.1700G>C	XP_024303446.1:p.Gly567Ala
XM_024447679.1:c.1700G>C	XP_024303447.1:p.Gly567Ala
XM_024447680.1:c.1535G>C	XP_024303448.1:p.Gly512Ala
NM_024757.5:c.1793G>C MANE Select	NP_079033.4:p.Gly598Ala
NM_001145527.2:c.1793G>C	NP_001138999.1:p.Gly598Ala
NM_001354259.2:c.1700G>C	NP_001341188.1:p.Gly567Ala
NM_001354263.2:c.1772G>C	NP_001341192.1:p.Gly591Ala