Canonical Allele Identifier: CA375776476

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671197T>A (hg19) ; chr9:g.137776745T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776745T>A , CM000671.2:g.137776745T>A	GRCh38
NC_000009.11:g.140671197T>A , CM000671.1:g.140671197T>A	GRCh37
NC_000009.10:g.139791018T>A	NCBI36
NG_011776.1:g.162754T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1919T>A MANE Select	ENSP00000417980.1:p.Val640Glu
ENST00000636027.1:c.1805T>A	ENSP00000489961.1:p.Val602Glu
ENST00000637161.1:c.1826T>A	ENSP00000490328.1:p.Val609Glu
ENST00000637261.1:c.1959T>A	ENSP00000490815.1:n.1959T>A
ENST00000638071.1:c.1546T>A
ENST00000640639.1:c.1088T>A	ENSP00000491823.1:p.Val363Glu
ENST00000371394.6:c.*1654T>A	ENSP00000485945.1:n.*1654T>A
ENST00000460843.5:c.1919T>A	ENSP00000417980.1:p.Val640Glu
ENST00000462484.5:c.1919T>A	ENSP00000417328.1:p.Val640Glu
ENST00000462942.3:c.776T>A	ENSP00000436107.1:p.Val259Glu
ENST00000465566.2:c.467T>A	ENSP00000486261.1:p.Val156Glu
ENST00000626603.1:n.1704A>T
NM_001145527.1:c.1919T>A	NP_001138999.1:p.Val640Glu
NM_024757.4:c.1919T>A	NP_079033.4:p.Val640Glu
XM_005266105.3:c.1910T>A	XP_005266162.1:p.Val637Glu
XM_005266110.1:c.1826T>A	XP_005266167.1:p.Val609Glu
XM_006717288.2:c.1901T>A	XP_006717351.1:p.Val634Glu
XM_011519021.1:c.1928T>A	XP_011517323.1:p.Val643Glu
XM_011519022.1:c.1925T>A	XP_011517324.1:p.Val642Glu
XM_011519023.1:c.1907T>A	XP_011517325.1:p.Val636Glu
XM_011519024.1:c.1850T>A	XP_011517326.1:p.Val617Glu
XM_011519025.1:c.1826T>A	XP_011517327.1:p.Val609Glu
XM_011519026.1:c.1784T>A	XP_011517328.1:p.Val595Glu
XM_011519027.1:c.1928T>A	XP_011517329.1:p.Val643Glu
XM_011519028.1:c.1928T>A	XP_011517330.1:p.Val643Glu
XM_011519029.1:c.350T>A	XP_011517331.1:p.Val117Glu
XM_011519033.1:c.1763T>A	XP_011517335.1:p.Val588Glu
NM_001354259.1:c.1826T>A	NP_001341188.1:p.Val609Glu
NM_001354263.1:c.1898T>A	NP_001341192.1:p.Val633Glu
XM_005266105.5:c.1910T>A	XP_005266162.1:p.Val637Glu
XM_011519021.3:c.1928T>A	XP_011517323.1:p.Val643Glu
XM_011519022.3:c.1925T>A	XP_011517324.1:p.Val642Glu
XM_011519023.3:c.1907T>A	XP_011517325.1:p.Val636Glu
XM_011519029.3:c.350T>A	XP_011517331.1:p.Val117Glu
XM_017015134.1:c.1904T>A	XP_016870623.1:p.Val635Glu
XM_017015136.2:c.1820T>A	XP_016870625.1:p.Val607Glu
XM_017015137.1:c.1805T>A	XP_016870626.1:p.Val602Glu
XM_017015138.1:c.1805T>A	XP_016870627.1:p.Val602Glu
XM_024447674.1:c.1748T>A	XP_024303442.1:p.Val583Glu
XM_024447675.1:c.1682T>A	XP_024303443.1:p.Val561Glu
XM_024447676.1:c.1043T>A	XP_024303444.1:p.Val348Glu
XM_024447677.1:c.1043T>A	XP_024303445.1:p.Val348Glu
XM_024447678.1:c.1826T>A	XP_024303446.1:p.Val609Glu
XM_024447679.1:c.1826T>A	XP_024303447.1:p.Val609Glu
XM_024447680.1:c.1661T>A	XP_024303448.1:p.Val554Glu
NM_024757.5:c.1919T>A MANE Select	NP_079033.4:p.Val640Glu
NM_001145527.2:c.1919T>A	NP_001138999.1:p.Val640Glu
NM_001354259.2:c.1826T>A	NP_001341188.1:p.Val609Glu
NM_001354263.2:c.1898T>A	NP_001341192.1:p.Val633Glu