Canonical Allele Identifier: CA467878056

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140712575T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137818123T>C , CM000671.2:g.137818123T>C	GRCh38
NC_000009.11:g.140712575T>C , CM000671.1:g.140712575T>C	GRCh37
NC_000009.10:g.139832396T>C	NCBI36
NG_011776.1:g.204132T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3525T>C MANE Select	ENSP00000417980.1:p.Phe1175=
ENST00000636472.1:n.87T>C
ENST00000636526.1:n.11T>C
ENST00000637161.1:c.3432T>C	ENSP00000490328.1:p.Phe1144=
ENST00000637261.1:c.4099T>C	ENSP00000490815.1:n.4099T>C
ENST00000637748.1:n.506T>C
ENST00000637891.1:c.1599T>C	ENSP00000490907.1:n.1599T>C
ENST00000460843.5:c.3525T>C	ENSP00000417980.1:p.Phe1175=
ENST00000462942.3:c.2382T>C	ENSP00000436107.1:p.Phe794=
ENST00000475564.5:n.1249T>C
ENST00000494249.5:n.878T>C
NM_024757.4:c.3525T>C	NP_079033.4:p.Phe1175=
XM_005266105.3:c.3516T>C	XP_005266162.1:p.Phe1172=
XM_005266110.1:c.3432T>C	XP_005266167.1:p.Phe1144=
XM_006717288.2:c.3507T>C	XP_006717351.1:p.Phe1169=
XM_011519021.1:c.3534T>C	XP_011517323.1:p.Phe1178=
XM_011519022.1:c.3531T>C	XP_011517324.1:p.Phe1177=
XM_011519023.1:c.3513T>C	XP_011517325.1:p.Phe1171=
XM_011519024.1:c.3456T>C	XP_011517326.1:p.Phe1152=
XM_011519025.1:c.3432T>C	XP_011517327.1:p.Phe1144=
XM_011519026.1:c.3390T>C	XP_011517328.1:p.Phe1130=
XM_011519029.1:c.1956T>C	XP_011517331.1:p.Phe652=
XM_011519030.1:c.1308T>C	XP_011517332.1:p.Phe436=
XM_011519031.1:c.1095T>C	XP_011517333.1:p.Phe365=
XM_011519032.1:c.1095T>C	XP_011517334.1:p.Phe365=
XM_011519033.1:c.3369T>C	XP_011517335.1:p.Phe1123=
XR_930459.1:n.5297-3561A>G
NM_001354263.1:c.3504T>C	NP_001341192.1:p.Phe1168=
XM_005266105.5:c.3516T>C	XP_005266162.1:p.Phe1172=
XM_011519021.3:c.3534T>C	XP_011517323.1:p.Phe1178=
XM_011519022.3:c.3531T>C	XP_011517324.1:p.Phe1177=
XM_011519023.3:c.3513T>C	XP_011517325.1:p.Phe1171=
XM_011519029.3:c.1956T>C	XP_011517331.1:p.Phe652=
XM_011519030.3:c.1308T>C	XP_011517332.1:p.Phe436=
XM_017015134.1:c.3510T>C	XP_016870623.1:p.Phe1170=
XM_017015136.2:c.3426T>C	XP_016870625.1:p.Phe1142=
XM_017015137.1:c.3411T>C	XP_016870626.1:p.Phe1137=
XM_017015138.1:c.3411T>C	XP_016870627.1:p.Phe1137=
XM_024447674.1:c.3354T>C	XP_024303442.1:p.Phe1118=
XM_024447675.1:c.3288T>C	XP_024303443.1:p.Phe1096=
XM_024447676.1:c.2649T>C	XP_024303444.1:p.Phe883=
XM_024447677.1:c.2649T>C	XP_024303445.1:p.Phe883=
XM_024447680.1:c.3267T>C	XP_024303448.1:p.Phe1089=
NM_024757.5:c.3525T>C MANE Select	NP_079033.4:p.Phe1175=
NM_001354263.2:c.3504T>C	NP_001341192.1:p.Phe1168=