Canonical Allele Identifier: CA375776584

Gene: EHMT1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1930A>T MANE Select	ENSP00000417980.1:p.Lys644Ter
ENST00000636027.1:c.1816A>T	ENSP00000489961.1:p.Lys606Ter
ENST00000637161.1:c.1837A>T	ENSP00000490328.1:p.Lys613Ter
ENST00000637261.1:c.1970A>T	ENSP00000490815.1:n.1970A>T
ENST00000638071.1:c.1557A>T
ENST00000640639.1:c.1099A>T	ENSP00000491823.1:p.Lys367Ter
ENST00000371394.6:c.*1665A>T	ENSP00000485945.1:n.*1665A>T
ENST00000460843.5:c.1930A>T	ENSP00000417980.1:p.Lys644Ter
ENST00000462484.5:c.1930A>T	ENSP00000417328.1:p.Lys644Ter
ENST00000462942.3:c.787A>T	ENSP00000436107.1:p.Lys263Ter
ENST00000465566.2:c.478A>T	ENSP00000486261.1:p.Lys160Ter
ENST00000626603.1:n.1693T>A
NM_001145527.1:c.1930A>T	NP_001138999.1:p.Lys644Ter
NM_024757.4:c.1930A>T	NP_079033.4:p.Lys644Ter
XM_005266105.3:c.1921A>T	XP_005266162.1:p.Lys641Ter
XM_005266110.1:c.1837A>T	XP_005266167.1:p.Lys613Ter
XM_006717288.2:c.1912A>T	XP_006717351.1:p.Lys638Ter
XM_011519021.1:c.1939A>T	XP_011517323.1:p.Lys647Ter
XM_011519022.1:c.1936A>T	XP_011517324.1:p.Lys646Ter
XM_011519023.1:c.1918A>T	XP_011517325.1:p.Lys640Ter
XM_011519024.1:c.1861A>T	XP_011517326.1:p.Lys621Ter
XM_011519025.1:c.1837A>T	XP_011517327.1:p.Lys613Ter
XM_011519026.1:c.1795A>T	XP_011517328.1:p.Lys599Ter
XM_011519027.1:c.1939A>T	XP_011517329.1:p.Lys647Ter
XM_011519028.1:c.1939A>T	XP_011517330.1:p.Lys647Ter
XM_011519029.1:c.361A>T	XP_011517331.1:p.Lys121Ter
XM_011519033.1:c.1774A>T	XP_011517335.1:p.Lys592Ter
NM_001354259.1:c.1837A>T	NP_001341188.1:p.Lys613Ter
NM_001354263.1:c.1909A>T	NP_001341192.1:p.Lys637Ter
XM_005266105.5:c.1921A>T	XP_005266162.1:p.Lys641Ter
XM_011519021.3:c.1939A>T	XP_011517323.1:p.Lys647Ter
XM_011519022.3:c.1936A>T	XP_011517324.1:p.Lys646Ter
XM_011519023.3:c.1918A>T	XP_011517325.1:p.Lys640Ter
XM_011519029.3:c.361A>T	XP_011517331.1:p.Lys121Ter
XM_017015134.1:c.1915A>T	XP_016870623.1:p.Lys639Ter
XM_017015136.2:c.1831A>T	XP_016870625.1:p.Lys611Ter
XM_017015137.1:c.1816A>T	XP_016870626.1:p.Lys606Ter
XM_017015138.1:c.1816A>T	XP_016870627.1:p.Lys606Ter
XM_024447674.1:c.1759A>T	XP_024303442.1:p.Lys587Ter
XM_024447675.1:c.1693A>T	XP_024303443.1:p.Lys565Ter
XM_024447676.1:c.1054A>T	XP_024303444.1:p.Lys352Ter
XM_024447677.1:c.1054A>T	XP_024303445.1:p.Lys352Ter
XM_024447678.1:c.1837A>T	XP_024303446.1:p.Lys613Ter
XM_024447679.1:c.1837A>T	XP_024303447.1:p.Lys613Ter
XM_024447680.1:c.1672A>T	XP_024303448.1:p.Lys558Ter
NM_024757.5:c.1930A>T MANE Select	NP_079033.4:p.Lys644Ter
NM_001145527.2:c.1930A>T	NP_001138999.1:p.Lys644Ter
NM_001354259.2:c.1837A>T	NP_001341188.1:p.Lys613Ter
NM_001354263.2:c.1909A>T	NP_001341192.1:p.Lys637Ter