Canonical Allele Identifier: CA375791476

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140705970A>G (hg19) ; chr9:g.137811518A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137811518A>G , CM000671.2:g.137811518A>G	GRCh38
NC_000009.11:g.140705970A>G , CM000671.1:g.140705970A>G	GRCh37
NC_000009.10:g.139825791A>G	NCBI36
NG_011776.1:g.197527A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000460843.6:c.2770A>G MANE Select	ENSP00000417980.1:p.Ile924Val
ENST00000636027.1:c.2656A>G	ENSP00000489961.1:p.Ile886Val
ENST00000637161.1:c.2677A>G	ENSP00000490328.1:p.Ile893Val
ENST00000637261.1:c.2810A>G	ENSP00000490815.1:n.2810A>G
ENST00000637891.1:c.664A>G	ENSP00000490907.1:p.Ile222Val
ENST00000460843.5:c.2770A>G	ENSP00000417980.1:p.Ile924Val
ENST00000462942.3:c.1627A>G	ENSP00000436107.1:p.Ile543Val
ENST00000486164.5:c.457A>G
ENST00000488242.2:n.296A>G
NM_024757.4:c.2770A>G	NP_079033.4:p.Ile924Val
XM_005266105.3:c.2761A>G	XP_005266162.1:p.Ile921Val
XM_005266110.1:c.2677A>G	XP_005266167.1:p.Ile893Val
XM_006717288.2:c.2752A>G	XP_006717351.1:p.Ile918Val
XM_011519021.1:c.2779A>G	XP_011517323.1:p.Ile927Val
XM_011519022.1:c.2776A>G	XP_011517324.1:p.Ile926Val
XM_011519023.1:c.2758A>G	XP_011517325.1:p.Ile920Val
XM_011519024.1:c.2701A>G	XP_011517326.1:p.Ile901Val
XM_011519025.1:c.2677A>G	XP_011517327.1:p.Ile893Val
XM_011519026.1:c.2635A>G	XP_011517328.1:p.Ile879Val
XM_011519029.1:c.1201A>G	XP_011517331.1:p.Ile401Val
XM_011519030.1:c.553A>G	XP_011517332.1:p.Ile185Val
XM_011519031.1:c.340A>G	XP_011517333.1:p.Ile114Val
XM_011519032.1:c.340A>G	XP_011517334.1:p.Ile114Val
XM_011519033.1:c.2614A>G	XP_011517335.1:p.Ile872Val
NM_001354263.1:c.2749A>G	NP_001341192.1:p.Ile917Val
XM_005266105.5:c.2761A>G	XP_005266162.1:p.Ile921Val
XM_011519021.3:c.2779A>G	XP_011517323.1:p.Ile927Val
XM_011519022.3:c.2776A>G	XP_011517324.1:p.Ile926Val
XM_011519023.3:c.2758A>G	XP_011517325.1:p.Ile920Val
XM_011519029.3:c.1201A>G	XP_011517331.1:p.Ile401Val
XM_011519030.3:c.553A>G	XP_011517332.1:p.Ile185Val
XM_017015134.1:c.2755A>G	XP_016870623.1:p.Ile919Val
XM_017015136.2:c.2671A>G	XP_016870625.1:p.Ile891Val
XM_017015137.1:c.2656A>G	XP_016870626.1:p.Ile886Val
XM_017015138.1:c.2656A>G	XP_016870627.1:p.Ile886Val
XM_024447674.1:c.2599A>G	XP_024303442.1:p.Ile867Val
XM_024447675.1:c.2533A>G	XP_024303443.1:p.Ile845Val
XM_024447676.1:c.1894A>G	XP_024303444.1:p.Ile632Val
XM_024447677.1:c.1894A>G	XP_024303445.1:p.Ile632Val
XM_024447680.1:c.2512A>G	XP_024303448.1:p.Ile838Val
NM_024757.5:c.2770A>G MANE Select	NP_079033.4:p.Ile924Val
NM_001354263.2:c.2749A>G	NP_001341192.1:p.Ile917Val