Canonical Allele Identifier: CA375776578

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671208A>C (hg19) ; chr9:g.137776756A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776756A>C , CM000671.2:g.137776756A>C	GRCh38
NC_000009.11:g.140671208A>C , CM000671.1:g.140671208A>C	GRCh37
NC_000009.10:g.139791029A>C	NCBI36
NG_011776.1:g.162765A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1930A>C MANE Select	ENSP00000417980.1:p.Lys644Gln
ENST00000636027.1:c.1816A>C	ENSP00000489961.1:p.Lys606Gln
ENST00000637161.1:c.1837A>C	ENSP00000490328.1:p.Lys613Gln
ENST00000637261.1:c.1970A>C	ENSP00000490815.1:n.1970A>C
ENST00000638071.1:c.1557A>C
ENST00000640639.1:c.1099A>C	ENSP00000491823.1:p.Lys367Gln
ENST00000371394.6:c.*1665A>C	ENSP00000485945.1:n.*1665A>C
ENST00000460843.5:c.1930A>C	ENSP00000417980.1:p.Lys644Gln
ENST00000462484.5:c.1930A>C	ENSP00000417328.1:p.Lys644Gln
ENST00000462942.3:c.787A>C	ENSP00000436107.1:p.Lys263Gln
ENST00000465566.2:c.478A>C	ENSP00000486261.1:p.Lys160Gln
ENST00000626603.1:n.1693T>G
NM_001145527.1:c.1930A>C	NP_001138999.1:p.Lys644Gln
NM_024757.4:c.1930A>C	NP_079033.4:p.Lys644Gln
XM_005266105.3:c.1921A>C	XP_005266162.1:p.Lys641Gln
XM_005266110.1:c.1837A>C	XP_005266167.1:p.Lys613Gln
XM_006717288.2:c.1912A>C	XP_006717351.1:p.Lys638Gln
XM_011519021.1:c.1939A>C	XP_011517323.1:p.Lys647Gln
XM_011519022.1:c.1936A>C	XP_011517324.1:p.Lys646Gln
XM_011519023.1:c.1918A>C	XP_011517325.1:p.Lys640Gln
XM_011519024.1:c.1861A>C	XP_011517326.1:p.Lys621Gln
XM_011519025.1:c.1837A>C	XP_011517327.1:p.Lys613Gln
XM_011519026.1:c.1795A>C	XP_011517328.1:p.Lys599Gln
XM_011519027.1:c.1939A>C	XP_011517329.1:p.Lys647Gln
XM_011519028.1:c.1939A>C	XP_011517330.1:p.Lys647Gln
XM_011519029.1:c.361A>C	XP_011517331.1:p.Lys121Gln
XM_011519033.1:c.1774A>C	XP_011517335.1:p.Lys592Gln
NM_001354259.1:c.1837A>C	NP_001341188.1:p.Lys613Gln
NM_001354263.1:c.1909A>C	NP_001341192.1:p.Lys637Gln
XM_005266105.5:c.1921A>C	XP_005266162.1:p.Lys641Gln
XM_011519021.3:c.1939A>C	XP_011517323.1:p.Lys647Gln
XM_011519022.3:c.1936A>C	XP_011517324.1:p.Lys646Gln
XM_011519023.3:c.1918A>C	XP_011517325.1:p.Lys640Gln
XM_011519029.3:c.361A>C	XP_011517331.1:p.Lys121Gln
XM_017015134.1:c.1915A>C	XP_016870623.1:p.Lys639Gln
XM_017015136.2:c.1831A>C	XP_016870625.1:p.Lys611Gln
XM_017015137.1:c.1816A>C	XP_016870626.1:p.Lys606Gln
XM_017015138.1:c.1816A>C	XP_016870627.1:p.Lys606Gln
XM_024447674.1:c.1759A>C	XP_024303442.1:p.Lys587Gln
XM_024447675.1:c.1693A>C	XP_024303443.1:p.Lys565Gln
XM_024447676.1:c.1054A>C	XP_024303444.1:p.Lys352Gln
XM_024447677.1:c.1054A>C	XP_024303445.1:p.Lys352Gln
XM_024447678.1:c.1837A>C	XP_024303446.1:p.Lys613Gln
XM_024447679.1:c.1837A>C	XP_024303447.1:p.Lys613Gln
XM_024447680.1:c.1672A>C	XP_024303448.1:p.Lys558Gln
NM_024757.5:c.1930A>C MANE Select	NP_079033.4:p.Lys644Gln
NM_001145527.2:c.1930A>C	NP_001138999.1:p.Lys644Gln
NM_001354259.2:c.1837A>C	NP_001341188.1:p.Lys613Gln
NM_001354263.2:c.1909A>C	NP_001341192.1:p.Lys637Gln