Canonical Allele Identifier: CA375793364

Gene: EHMT1

Linked Data

• dbSNP Id: rs2137711171
• MyVariant Identifiers: chr9:g.140707509G>C (hg19) ; chr9:g.137813057G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813057G>C , CM000671.2:g.137813057G>C	GRCh38
NC_000009.11:g.140707509G>C , CM000671.1:g.140707509G>C	GRCh37
NC_000009.10:g.139827330G>C	NCBI36
NG_011776.1:g.199066G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2919G>C MANE Select	ENSP00000417980.1:p.Glu973Asp
ENST00000636027.1:c.2805G>C	ENSP00000489961.1:p.Glu935Asp
ENST00000637161.1:c.2826G>C	ENSP00000490328.1:p.Glu942Asp
ENST00000637261.1:c.2959G>C	ENSP00000490815.1:n.2959G>C
ENST00000637891.1:c.813G>C	ENSP00000490907.1:p.Glu271Asp
ENST00000460843.5:c.2919G>C	ENSP00000417980.1:p.Glu973Asp
ENST00000462942.3:c.1776G>C	ENSP00000436107.1:p.Glu592Asp
ENST00000486164.5:c.606G>C
ENST00000488242.2:n.445G>C
NM_024757.4:c.2919G>C	NP_079033.4:p.Glu973Asp
XM_005266105.3:c.2910G>C	XP_005266162.1:p.Glu970Asp
XM_005266110.1:c.2826G>C	XP_005266167.1:p.Glu942Asp
XM_006717288.2:c.2901G>C	XP_006717351.1:p.Glu967Asp
XM_011519021.1:c.2928G>C	XP_011517323.1:p.Glu976Asp
XM_011519022.1:c.2925G>C	XP_011517324.1:p.Glu975Asp
XM_011519023.1:c.2907G>C	XP_011517325.1:p.Glu969Asp
XM_011519024.1:c.2850G>C	XP_011517326.1:p.Glu950Asp
XM_011519025.1:c.2826G>C	XP_011517327.1:p.Glu942Asp
XM_011519026.1:c.2784G>C	XP_011517328.1:p.Glu928Asp
XM_011519029.1:c.1350G>C	XP_011517331.1:p.Glu450Asp
XM_011519030.1:c.702G>C	XP_011517332.1:p.Glu234Asp
XM_011519031.1:c.489G>C	XP_011517333.1:p.Glu163Asp
XM_011519032.1:c.489G>C	XP_011517334.1:p.Glu163Asp
XM_011519033.1:c.2763G>C	XP_011517335.1:p.Glu921Asp
NM_001354263.1:c.2898G>C	NP_001341192.1:p.Glu966Asp
XM_005266105.5:c.2910G>C	XP_005266162.1:p.Glu970Asp
XM_011519021.3:c.2928G>C	XP_011517323.1:p.Glu976Asp
XM_011519022.3:c.2925G>C	XP_011517324.1:p.Glu975Asp
XM_011519023.3:c.2907G>C	XP_011517325.1:p.Glu969Asp
XM_011519029.3:c.1350G>C	XP_011517331.1:p.Glu450Asp
XM_011519030.3:c.702G>C	XP_011517332.1:p.Glu234Asp
XM_017015134.1:c.2904G>C	XP_016870623.1:p.Glu968Asp
XM_017015136.2:c.2820G>C	XP_016870625.1:p.Glu940Asp
XM_017015137.1:c.2805G>C	XP_016870626.1:p.Glu935Asp
XM_017015138.1:c.2805G>C	XP_016870627.1:p.Glu935Asp
XM_024447674.1:c.2748G>C	XP_024303442.1:p.Glu916Asp
XM_024447675.1:c.2682G>C	XP_024303443.1:p.Glu894Asp
XM_024447676.1:c.2043G>C	XP_024303444.1:p.Glu681Asp
XM_024447677.1:c.2043G>C	XP_024303445.1:p.Glu681Asp
XM_024447680.1:c.2661G>C	XP_024303448.1:p.Glu887Asp
NM_024757.5:c.2919G>C MANE Select	NP_079033.4:p.Glu973Asp
NM_001354263.2:c.2898G>C	NP_001341192.1:p.Glu966Asp