Canonical Allele Identifier: CA375776789

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671241C>A (hg19) ; chr9:g.137776789C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776789C>A , CM000671.2:g.137776789C>A	GRCh38
NC_000009.11:g.140671241C>A , CM000671.1:g.140671241C>A	GRCh37
NC_000009.10:g.139791062C>A	NCBI36
NG_011776.1:g.162798C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1963C>A MANE Select	ENSP00000417980.1:p.Pro655Thr
ENST00000636027.1:c.1849C>A	ENSP00000489961.1:p.Pro617Thr
ENST00000637161.1:c.1870C>A	ENSP00000490328.1:p.Pro624Thr
ENST00000637261.1:c.2003C>A	ENSP00000490815.1:n.2003C>A
ENST00000638071.1:c.1590C>A
ENST00000640639.1:c.1132C>A	ENSP00000491823.1:p.Pro378Thr
ENST00000371394.6:c.*1698C>A	ENSP00000485945.1:n.*1698C>A
ENST00000460843.5:c.1963C>A	ENSP00000417980.1:p.Pro655Thr
ENST00000462484.5:c.1963C>A	ENSP00000417328.1:p.Pro655Thr
ENST00000462942.3:c.820C>A	ENSP00000436107.1:p.Pro274Thr
ENST00000626603.1:n.1660G>T
NM_001145527.1:c.1963C>A	NP_001138999.1:p.Pro655Thr
NM_024757.4:c.1963C>A	NP_079033.4:p.Pro655Thr
XM_005266105.3:c.1954C>A	XP_005266162.1:p.Pro652Thr
XM_005266110.1:c.1870C>A	XP_005266167.1:p.Pro624Thr
XM_006717288.2:c.1945C>A	XP_006717351.1:p.Pro649Thr
XM_011519021.1:c.1972C>A	XP_011517323.1:p.Pro658Thr
XM_011519022.1:c.1969C>A	XP_011517324.1:p.Pro657Thr
XM_011519023.1:c.1951C>A	XP_011517325.1:p.Pro651Thr
XM_011519024.1:c.1894C>A	XP_011517326.1:p.Pro632Thr
XM_011519025.1:c.1870C>A	XP_011517327.1:p.Pro624Thr
XM_011519026.1:c.1828C>A	XP_011517328.1:p.Pro610Thr
XM_011519027.1:c.1972C>A	XP_011517329.1:p.Pro658Thr
XM_011519028.1:c.1972C>A	XP_011517330.1:p.Pro658Thr
XM_011519029.1:c.394C>A	XP_011517331.1:p.Pro132Thr
XM_011519033.1:c.1807C>A	XP_011517335.1:p.Pro603Thr
NM_001354259.1:c.1870C>A	NP_001341188.1:p.Pro624Thr
NM_001354263.1:c.1942C>A	NP_001341192.1:p.Pro648Thr
XM_005266105.5:c.1954C>A	XP_005266162.1:p.Pro652Thr
XM_011519021.3:c.1972C>A	XP_011517323.1:p.Pro658Thr
XM_011519022.3:c.1969C>A	XP_011517324.1:p.Pro657Thr
XM_011519023.3:c.1951C>A	XP_011517325.1:p.Pro651Thr
XM_011519029.3:c.394C>A	XP_011517331.1:p.Pro132Thr
XM_017015134.1:c.1948C>A	XP_016870623.1:p.Pro650Thr
XM_017015136.2:c.1864C>A	XP_016870625.1:p.Pro622Thr
XM_017015137.1:c.1849C>A	XP_016870626.1:p.Pro617Thr
XM_017015138.1:c.1849C>A	XP_016870627.1:p.Pro617Thr
XM_024447674.1:c.1792C>A	XP_024303442.1:p.Pro598Thr
XM_024447675.1:c.1726C>A	XP_024303443.1:p.Pro576Thr
XM_024447676.1:c.1087C>A	XP_024303444.1:p.Pro363Thr
XM_024447677.1:c.1087C>A	XP_024303445.1:p.Pro363Thr
XM_024447678.1:c.1870C>A	XP_024303446.1:p.Pro624Thr
XM_024447679.1:c.1870C>A	XP_024303447.1:p.Pro624Thr
XM_024447680.1:c.1705C>A	XP_024303448.1:p.Pro569Thr
NM_024757.5:c.1963C>A MANE Select	NP_079033.4:p.Pro655Thr
NM_001145527.2:c.1963C>A	NP_001138999.1:p.Pro655Thr
NM_001354259.2:c.1870C>A	NP_001341188.1:p.Pro624Thr
NM_001354263.2:c.1942C>A	NP_001341192.1:p.Pro648Thr