Canonical Allele Identifier: CA375793354

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707504G>T (hg19) ; chr9:g.137813052G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813052G>T , CM000671.2:g.137813052G>T	GRCh38
NC_000009.11:g.140707504G>T , CM000671.1:g.140707504G>T	GRCh37
NC_000009.10:g.139827325G>T	NCBI36
NG_011776.1:g.199061G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2914G>T MANE Select	ENSP00000417980.1:p.Gly972Ter
ENST00000636027.1:c.2800G>T	ENSP00000489961.1:p.Gly934Ter
ENST00000637161.1:c.2821G>T	ENSP00000490328.1:p.Gly941Ter
ENST00000637261.1:c.2954G>T	ENSP00000490815.1:n.2954G>T
ENST00000637891.1:c.808G>T	ENSP00000490907.1:p.Gly270Ter
ENST00000460843.5:c.2914G>T	ENSP00000417980.1:p.Gly972Ter
ENST00000462942.3:c.1771G>T	ENSP00000436107.1:p.Gly591Ter
ENST00000486164.5:c.601G>T
ENST00000488242.2:n.440G>T
NM_024757.4:c.2914G>T	NP_079033.4:p.Gly972Ter
XM_005266105.3:c.2905G>T	XP_005266162.1:p.Gly969Ter
XM_005266110.1:c.2821G>T	XP_005266167.1:p.Gly941Ter
XM_006717288.2:c.2896G>T	XP_006717351.1:p.Gly966Ter
XM_011519021.1:c.2923G>T	XP_011517323.1:p.Gly975Ter
XM_011519022.1:c.2920G>T	XP_011517324.1:p.Gly974Ter
XM_011519023.1:c.2902G>T	XP_011517325.1:p.Gly968Ter
XM_011519024.1:c.2845G>T	XP_011517326.1:p.Gly949Ter
XM_011519025.1:c.2821G>T	XP_011517327.1:p.Gly941Ter
XM_011519026.1:c.2779G>T	XP_011517328.1:p.Gly927Ter
XM_011519029.1:c.1345G>T	XP_011517331.1:p.Gly449Ter
XM_011519030.1:c.697G>T	XP_011517332.1:p.Gly233Ter
XM_011519031.1:c.484G>T	XP_011517333.1:p.Gly162Ter
XM_011519032.1:c.484G>T	XP_011517334.1:p.Gly162Ter
XM_011519033.1:c.2758G>T	XP_011517335.1:p.Gly920Ter
NM_001354263.1:c.2893G>T	NP_001341192.1:p.Gly965Ter
XM_005266105.5:c.2905G>T	XP_005266162.1:p.Gly969Ter
XM_011519021.3:c.2923G>T	XP_011517323.1:p.Gly975Ter
XM_011519022.3:c.2920G>T	XP_011517324.1:p.Gly974Ter
XM_011519023.3:c.2902G>T	XP_011517325.1:p.Gly968Ter
XM_011519029.3:c.1345G>T	XP_011517331.1:p.Gly449Ter
XM_011519030.3:c.697G>T	XP_011517332.1:p.Gly233Ter
XM_017015134.1:c.2899G>T	XP_016870623.1:p.Gly967Ter
XM_017015136.2:c.2815G>T	XP_016870625.1:p.Gly939Ter
XM_017015137.1:c.2800G>T	XP_016870626.1:p.Gly934Ter
XM_017015138.1:c.2800G>T	XP_016870627.1:p.Gly934Ter
XM_024447674.1:c.2743G>T	XP_024303442.1:p.Gly915Ter
XM_024447675.1:c.2677G>T	XP_024303443.1:p.Gly893Ter
XM_024447676.1:c.2038G>T	XP_024303444.1:p.Gly680Ter
XM_024447677.1:c.2038G>T	XP_024303445.1:p.Gly680Ter
XM_024447680.1:c.2656G>T	XP_024303448.1:p.Gly886Ter
NM_024757.5:c.2914G>T MANE Select	NP_079033.4:p.Gly972Ter
NM_001354263.2:c.2893G>T	NP_001341192.1:p.Gly965Ter