Canonical Allele Identifier: CA375776876

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671256G>A (hg19) ; chr9:g.137776804G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776804G>A , CM000671.2:g.137776804G>A	GRCh38
NC_000009.11:g.140671256G>A , CM000671.1:g.140671256G>A	GRCh37
NC_000009.10:g.139791077G>A	NCBI36
NG_011776.1:g.162813G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1978G>A MANE Select	ENSP00000417980.1:p.Gly660Ser
ENST00000636027.1:c.1864G>A	ENSP00000489961.1:p.Gly622Ser
ENST00000637161.1:c.1885G>A	ENSP00000490328.1:p.Gly629Ser
ENST00000637261.1:c.2018G>A	ENSP00000490815.1:n.2018G>A
ENST00000638071.1:c.1605G>A
ENST00000640639.1:c.1147G>A	ENSP00000491823.1:p.Gly383Ser
ENST00000371394.6:c.*1713G>A	ENSP00000485945.1:n.*1713G>A
ENST00000460843.5:c.1978G>A	ENSP00000417980.1:p.Gly660Ser
ENST00000462484.5:c.1978G>A	ENSP00000417328.1:p.Gly660Ser
ENST00000462942.3:c.835G>A	ENSP00000436107.1:p.Gly279Ser
ENST00000626603.1:n.1645C>T
NM_001145527.1:c.1978G>A	NP_001138999.1:p.Gly660Ser
NM_024757.4:c.1978G>A	NP_079033.4:p.Gly660Ser
XM_005266105.3:c.1969G>A	XP_005266162.1:p.Gly657Ser
XM_005266110.1:c.1885G>A	XP_005266167.1:p.Gly629Ser
XM_006717288.2:c.1960G>A	XP_006717351.1:p.Gly654Ser
XM_011519021.1:c.1987G>A	XP_011517323.1:p.Gly663Ser
XM_011519022.1:c.1984G>A	XP_011517324.1:p.Gly662Ser
XM_011519023.1:c.1966G>A	XP_011517325.1:p.Gly656Ser
XM_011519024.1:c.1909G>A	XP_011517326.1:p.Gly637Ser
XM_011519025.1:c.1885G>A	XP_011517327.1:p.Gly629Ser
XM_011519026.1:c.1843G>A	XP_011517328.1:p.Gly615Ser
XM_011519027.1:c.1987G>A	XP_011517329.1:p.Gly663Ser
XM_011519028.1:c.1987G>A	XP_011517330.1:p.Gly663Ser
XM_011519029.1:c.409G>A	XP_011517331.1:p.Gly137Ser
XM_011519033.1:c.1822G>A	XP_011517335.1:p.Gly608Ser
NM_001354259.1:c.1885G>A	NP_001341188.1:p.Gly629Ser
NM_001354263.1:c.1957G>A	NP_001341192.1:p.Gly653Ser
XM_005266105.5:c.1969G>A	XP_005266162.1:p.Gly657Ser
XM_011519021.3:c.1987G>A	XP_011517323.1:p.Gly663Ser
XM_011519022.3:c.1984G>A	XP_011517324.1:p.Gly662Ser
XM_011519023.3:c.1966G>A	XP_011517325.1:p.Gly656Ser
XM_011519029.3:c.409G>A	XP_011517331.1:p.Gly137Ser
XM_017015134.1:c.1963G>A	XP_016870623.1:p.Gly655Ser
XM_017015136.2:c.1879G>A	XP_016870625.1:p.Gly627Ser
XM_017015137.1:c.1864G>A	XP_016870626.1:p.Gly622Ser
XM_017015138.1:c.1864G>A	XP_016870627.1:p.Gly622Ser
XM_024447674.1:c.1807G>A	XP_024303442.1:p.Gly603Ser
XM_024447675.1:c.1741G>A	XP_024303443.1:p.Gly581Ser
XM_024447676.1:c.1102G>A	XP_024303444.1:p.Gly368Ser
XM_024447677.1:c.1102G>A	XP_024303445.1:p.Gly368Ser
XM_024447678.1:c.1885G>A	XP_024303446.1:p.Gly629Ser
XM_024447679.1:c.1885G>A	XP_024303447.1:p.Gly629Ser
XM_024447680.1:c.1720G>A	XP_024303448.1:p.Gly574Ser
NM_024757.5:c.1978G>A MANE Select	NP_079033.4:p.Gly660Ser
NM_001145527.2:c.1978G>A	NP_001138999.1:p.Gly660Ser
NM_001354259.2:c.1885G>A	NP_001341188.1:p.Gly629Ser
NM_001354263.2:c.1957G>A	NP_001341192.1:p.Gly653Ser