Canonical Allele Identifier: CA375773879

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140712576G>C (hg19) ; chr9:g.137818124G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137818124G>C , CM000671.2:g.137818124G>C	GRCh38
NC_000009.11:g.140712576G>C , CM000671.1:g.140712576G>C	GRCh37
NC_000009.10:g.139832397G>C	NCBI36
NG_011776.1:g.204133G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3526G>C MANE Select	ENSP00000417980.1:p.Asp1176His
ENST00000636472.1:n.88G>C
ENST00000636526.1:n.12G>C
ENST00000637161.1:c.3433G>C	ENSP00000490328.1:p.Asp1145His
ENST00000637261.1:c.4100G>C	ENSP00000490815.1:n.4100G>C
ENST00000637748.1:n.507G>C
ENST00000637891.1:c.1600G>C	ENSP00000490907.1:n.1600G>C
ENST00000460843.5:c.3526G>C	ENSP00000417980.1:p.Asp1176His
ENST00000462942.3:c.2383G>C	ENSP00000436107.1:p.Asp795His
ENST00000475564.5:n.1250G>C
ENST00000494249.5:n.879G>C
NM_024757.4:c.3526G>C	NP_079033.4:p.Asp1176His
XM_005266105.3:c.3517G>C	XP_005266162.1:p.Asp1173His
XM_005266110.1:c.3433G>C	XP_005266167.1:p.Asp1145His
XM_006717288.2:c.3508G>C	XP_006717351.1:p.Asp1170His
XM_011519021.1:c.3535G>C	XP_011517323.1:p.Asp1179His
XM_011519022.1:c.3532G>C	XP_011517324.1:p.Asp1178His
XM_011519023.1:c.3514G>C	XP_011517325.1:p.Asp1172His
XM_011519024.1:c.3457G>C	XP_011517326.1:p.Asp1153His
XM_011519025.1:c.3433G>C	XP_011517327.1:p.Asp1145His
XM_011519026.1:c.3391G>C	XP_011517328.1:p.Asp1131His
XM_011519029.1:c.1957G>C	XP_011517331.1:p.Asp653His
XM_011519030.1:c.1309G>C	XP_011517332.1:p.Asp437His
XM_011519031.1:c.1096G>C	XP_011517333.1:p.Asp366His
XM_011519032.1:c.1096G>C	XP_011517334.1:p.Asp366His
XM_011519033.1:c.3370G>C	XP_011517335.1:p.Asp1124His
XR_930459.1:n.5297-3562C>G
NM_001354263.1:c.3505G>C	NP_001341192.1:p.Asp1169His
XM_005266105.5:c.3517G>C	XP_005266162.1:p.Asp1173His
XM_011519021.3:c.3535G>C	XP_011517323.1:p.Asp1179His
XM_011519022.3:c.3532G>C	XP_011517324.1:p.Asp1178His
XM_011519023.3:c.3514G>C	XP_011517325.1:p.Asp1172His
XM_011519029.3:c.1957G>C	XP_011517331.1:p.Asp653His
XM_011519030.3:c.1309G>C	XP_011517332.1:p.Asp437His
XM_017015134.1:c.3511G>C	XP_016870623.1:p.Asp1171His
XM_017015136.2:c.3427G>C	XP_016870625.1:p.Asp1143His
XM_017015137.1:c.3412G>C	XP_016870626.1:p.Asp1138His
XM_017015138.1:c.3412G>C	XP_016870627.1:p.Asp1138His
XM_024447674.1:c.3355G>C	XP_024303442.1:p.Asp1119His
XM_024447675.1:c.3289G>C	XP_024303443.1:p.Asp1097His
XM_024447676.1:c.2650G>C	XP_024303444.1:p.Asp884His
XM_024447677.1:c.2650G>C	XP_024303445.1:p.Asp884His
XM_024447680.1:c.3268G>C	XP_024303448.1:p.Asp1090His
NM_024757.5:c.3526G>C MANE Select	NP_079033.4:p.Asp1176His
NM_001354263.2:c.3505G>C	NP_001341192.1:p.Asp1169His