Canonical Allele Identifier: CA375796778

Gene: EHMT1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137816034C>T , CM000671.2:g.137816034C>T	GRCh38
NC_000009.11:g.140710486C>T , CM000671.1:g.140710486C>T	GRCh37
NC_000009.10:g.139830307C>T	NCBI36
NG_011776.1:g.202043C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3346C>T MANE Select	ENSP00000417980.1:p.Arg1116Ter
ENST00000635741.1:n.35C>T
ENST00000637161.1:c.3253C>T	ENSP00000490328.1:p.Arg1085Ter
ENST00000637261.1:c.3386C>T	ENSP00000490815.1:n.3386C>T
ENST00000637748.1:n.283C>T
ENST00000637891.1:c.1420C>T	ENSP00000490907.1:n.1420C>T
ENST00000460843.5:c.3346C>T	ENSP00000417980.1:p.Arg1116Ter
ENST00000462942.3:c.2203C>T	ENSP00000436107.1:p.Arg735Ter
ENST00000494249.5:n.699C>T
NM_024757.4:c.3346C>T	NP_079033.4:p.Arg1116Ter
XM_005266105.3:c.3337C>T	XP_005266162.1:p.Arg1113Ter
XM_005266110.1:c.3253C>T	XP_005266167.1:p.Arg1085Ter
XM_006717288.2:c.3328C>T	XP_006717351.1:p.Arg1110Ter
XM_011519021.1:c.3355C>T	XP_011517323.1:p.Arg1119Ter
XM_011519022.1:c.3352C>T	XP_011517324.1:p.Arg1118Ter
XM_011519023.1:c.3334C>T	XP_011517325.1:p.Arg1112Ter
XM_011519024.1:c.3277C>T	XP_011517326.1:p.Arg1093Ter
XM_011519025.1:c.3253C>T	XP_011517327.1:p.Arg1085Ter
XM_011519026.1:c.3211C>T	XP_011517328.1:p.Arg1071Ter
XM_011519029.1:c.1777C>T	XP_011517331.1:p.Arg593Ter
XM_011519030.1:c.1129C>T	XP_011517332.1:p.Arg377Ter
XM_011519031.1:c.916C>T	XP_011517333.1:p.Arg306Ter
XM_011519032.1:c.916C>T	XP_011517334.1:p.Arg306Ter
XM_011519033.1:c.3190C>T	XP_011517335.1:p.Arg1064Ter
XR_930459.1:n.5297-1472G>A
NM_001354263.1:c.3325C>T	NP_001341192.1:p.Arg1109Ter
XM_005266105.5:c.3337C>T	XP_005266162.1:p.Arg1113Ter
XM_011519021.3:c.3355C>T	XP_011517323.1:p.Arg1119Ter
XM_011519022.3:c.3352C>T	XP_011517324.1:p.Arg1118Ter
XM_011519023.3:c.3334C>T	XP_011517325.1:p.Arg1112Ter
XM_011519029.3:c.1777C>T	XP_011517331.1:p.Arg593Ter
XM_011519030.3:c.1129C>T	XP_011517332.1:p.Arg377Ter
XM_017015134.1:c.3331C>T	XP_016870623.1:p.Arg1111Ter
XM_017015136.2:c.3247C>T	XP_016870625.1:p.Arg1083Ter
XM_017015137.1:c.3232C>T	XP_016870626.1:p.Arg1078Ter
XM_017015138.1:c.3232C>T	XP_016870627.1:p.Arg1078Ter
XM_024447674.1:c.3175C>T	XP_024303442.1:p.Arg1059Ter
XM_024447675.1:c.3109C>T	XP_024303443.1:p.Arg1037Ter
XM_024447676.1:c.2470C>T	XP_024303444.1:p.Arg824Ter
XM_024447677.1:c.2470C>T	XP_024303445.1:p.Arg824Ter
XM_024447680.1:c.3088C>T	XP_024303448.1:p.Arg1030Ter
NM_024757.5:c.3346C>T MANE Select	NP_079033.4:p.Arg1116Ter
NM_001354263.2:c.3325C>T	NP_001341192.1:p.Arg1109Ter