Canonical Allele Identifier: CA375793886

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707859G>C (hg19) ; chr9:g.137813407G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813407G>C , CM000671.2:g.137813407G>C	GRCh38
NC_000009.11:g.140707859G>C , CM000671.1:g.140707859G>C	GRCh37
NC_000009.10:g.139827680G>C	NCBI36
NG_011776.1:g.199416G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3057G>C MANE Select	ENSP00000417980.1:p.Glu1019Asp
ENST00000636027.1:c.2943G>C	ENSP00000489961.1:p.Glu981Asp
ENST00000637161.1:c.2964G>C	ENSP00000490328.1:p.Glu988Asp
ENST00000637261.1:c.3097G>C	ENSP00000490815.1:n.3097G>C
ENST00000637891.1:c.951G>C	ENSP00000490907.1:p.Glu317Asp
ENST00000460843.5:c.3057G>C	ENSP00000417980.1:p.Glu1019Asp
ENST00000462942.3:c.1914G>C	ENSP00000436107.1:p.Glu638Asp
ENST00000486164.5:c.744G>C
ENST00000488242.2:n.583G>C
NM_024757.4:c.3057G>C	NP_079033.4:p.Glu1019Asp
XM_005266105.3:c.3048G>C	XP_005266162.1:p.Glu1016Asp
XM_005266110.1:c.2964G>C	XP_005266167.1:p.Glu988Asp
XM_006717288.2:c.3039G>C	XP_006717351.1:p.Glu1013Asp
XM_011519021.1:c.3066G>C	XP_011517323.1:p.Glu1022Asp
XM_011519022.1:c.3063G>C	XP_011517324.1:p.Glu1021Asp
XM_011519023.1:c.3045G>C	XP_011517325.1:p.Glu1015Asp
XM_011519024.1:c.2988G>C	XP_011517326.1:p.Glu996Asp
XM_011519025.1:c.2964G>C	XP_011517327.1:p.Glu988Asp
XM_011519026.1:c.2922G>C	XP_011517328.1:p.Glu974Asp
XM_011519029.1:c.1488G>C	XP_011517331.1:p.Glu496Asp
XM_011519030.1:c.840G>C	XP_011517332.1:p.Glu280Asp
XM_011519031.1:c.627G>C	XP_011517333.1:p.Glu209Asp
XM_011519032.1:c.627G>C	XP_011517334.1:p.Glu209Asp
XM_011519033.1:c.2901G>C	XP_011517335.1:p.Glu967Asp
NM_001354263.1:c.3036G>C	NP_001341192.1:p.Glu1012Asp
XM_005266105.5:c.3048G>C	XP_005266162.1:p.Glu1016Asp
XM_011519021.3:c.3066G>C	XP_011517323.1:p.Glu1022Asp
XM_011519022.3:c.3063G>C	XP_011517324.1:p.Glu1021Asp
XM_011519023.3:c.3045G>C	XP_011517325.1:p.Glu1015Asp
XM_011519029.3:c.1488G>C	XP_011517331.1:p.Glu496Asp
XM_011519030.3:c.840G>C	XP_011517332.1:p.Glu280Asp
XM_017015134.1:c.3042G>C	XP_016870623.1:p.Glu1014Asp
XM_017015136.2:c.2958G>C	XP_016870625.1:p.Glu986Asp
XM_017015137.1:c.2943G>C	XP_016870626.1:p.Glu981Asp
XM_017015138.1:c.2943G>C	XP_016870627.1:p.Glu981Asp
XM_024447674.1:c.2886G>C	XP_024303442.1:p.Glu962Asp
XM_024447675.1:c.2820G>C	XP_024303443.1:p.Glu940Asp
XM_024447676.1:c.2181G>C	XP_024303444.1:p.Glu727Asp
XM_024447677.1:c.2181G>C	XP_024303445.1:p.Glu727Asp
XM_024447680.1:c.2799G>C	XP_024303448.1:p.Glu933Asp
NM_024757.5:c.3057G>C MANE Select	NP_079033.4:p.Glu1019Asp
NM_001354263.2:c.3036G>C	NP_001341192.1:p.Glu1012Asp