Canonical Allele Identifier: CA375776760

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671235C>A (hg19) ; chr9:g.137776783C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776783C>A , CM000671.2:g.137776783C>A	GRCh38
NC_000009.11:g.140671235C>A , CM000671.1:g.140671235C>A	GRCh37
NC_000009.10:g.139791056C>A	NCBI36
NG_011776.1:g.162792C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1957C>A MANE Select	ENSP00000417980.1:p.Pro653Thr
ENST00000636027.1:c.1843C>A	ENSP00000489961.1:p.Pro615Thr
ENST00000637161.1:c.1864C>A	ENSP00000490328.1:p.Pro622Thr
ENST00000637261.1:c.1997C>A	ENSP00000490815.1:n.1997C>A
ENST00000638071.1:c.1584C>A
ENST00000640639.1:c.1126C>A	ENSP00000491823.1:p.Pro376Thr
ENST00000371394.6:c.*1692C>A	ENSP00000485945.1:n.*1692C>A
ENST00000460843.5:c.1957C>A	ENSP00000417980.1:p.Pro653Thr
ENST00000462484.5:c.1957C>A	ENSP00000417328.1:p.Pro653Thr
ENST00000462942.3:c.814C>A	ENSP00000436107.1:p.Pro272Thr
ENST00000626603.1:n.1666G>T
NM_001145527.1:c.1957C>A	NP_001138999.1:p.Pro653Thr
NM_024757.4:c.1957C>A	NP_079033.4:p.Pro653Thr
XM_005266105.3:c.1948C>A	XP_005266162.1:p.Pro650Thr
XM_005266110.1:c.1864C>A	XP_005266167.1:p.Pro622Thr
XM_006717288.2:c.1939C>A	XP_006717351.1:p.Pro647Thr
XM_011519021.1:c.1966C>A	XP_011517323.1:p.Pro656Thr
XM_011519022.1:c.1963C>A	XP_011517324.1:p.Pro655Thr
XM_011519023.1:c.1945C>A	XP_011517325.1:p.Pro649Thr
XM_011519024.1:c.1888C>A	XP_011517326.1:p.Pro630Thr
XM_011519025.1:c.1864C>A	XP_011517327.1:p.Pro622Thr
XM_011519026.1:c.1822C>A	XP_011517328.1:p.Pro608Thr
XM_011519027.1:c.1966C>A	XP_011517329.1:p.Pro656Thr
XM_011519028.1:c.1966C>A	XP_011517330.1:p.Pro656Thr
XM_011519029.1:c.388C>A	XP_011517331.1:p.Pro130Thr
XM_011519033.1:c.1801C>A	XP_011517335.1:p.Pro601Thr
NM_001354259.1:c.1864C>A	NP_001341188.1:p.Pro622Thr
NM_001354263.1:c.1936C>A	NP_001341192.1:p.Pro646Thr
XM_005266105.5:c.1948C>A	XP_005266162.1:p.Pro650Thr
XM_011519021.3:c.1966C>A	XP_011517323.1:p.Pro656Thr
XM_011519022.3:c.1963C>A	XP_011517324.1:p.Pro655Thr
XM_011519023.3:c.1945C>A	XP_011517325.1:p.Pro649Thr
XM_011519029.3:c.388C>A	XP_011517331.1:p.Pro130Thr
XM_017015134.1:c.1942C>A	XP_016870623.1:p.Pro648Thr
XM_017015136.2:c.1858C>A	XP_016870625.1:p.Pro620Thr
XM_017015137.1:c.1843C>A	XP_016870626.1:p.Pro615Thr
XM_017015138.1:c.1843C>A	XP_016870627.1:p.Pro615Thr
XM_024447674.1:c.1786C>A	XP_024303442.1:p.Pro596Thr
XM_024447675.1:c.1720C>A	XP_024303443.1:p.Pro574Thr
XM_024447676.1:c.1081C>A	XP_024303444.1:p.Pro361Thr
XM_024447677.1:c.1081C>A	XP_024303445.1:p.Pro361Thr
XM_024447678.1:c.1864C>A	XP_024303446.1:p.Pro622Thr
XM_024447679.1:c.1864C>A	XP_024303447.1:p.Pro622Thr
XM_024447680.1:c.1699C>A	XP_024303448.1:p.Pro567Thr
NM_024757.5:c.1957C>A MANE Select	NP_079033.4:p.Pro653Thr
NM_001145527.2:c.1957C>A	NP_001138999.1:p.Pro653Thr
NM_001354259.2:c.1864C>A	NP_001341188.1:p.Pro622Thr
NM_001354263.2:c.1936C>A	NP_001341192.1:p.Pro646Thr