Canonical Allele Identifier: CA375793175

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707462T>G (hg19) ; chr9:g.137813010T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813010T>G , CM000671.2:g.137813010T>G	GRCh38
NC_000009.11:g.140707462T>G , CM000671.1:g.140707462T>G	GRCh37
NC_000009.10:g.139827283T>G	NCBI36
NG_011776.1:g.199019T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2872T>G MANE Select	ENSP00000417980.1:p.Phe958Val
ENST00000636027.1:c.2758T>G	ENSP00000489961.1:p.Phe920Val
ENST00000637161.1:c.2779T>G	ENSP00000490328.1:p.Phe927Val
ENST00000637261.1:c.2912T>G	ENSP00000490815.1:n.2912T>G
ENST00000637891.1:c.766T>G	ENSP00000490907.1:p.Phe256Val
ENST00000460843.5:c.2872T>G	ENSP00000417980.1:p.Phe958Val
ENST00000462942.3:c.1729T>G	ENSP00000436107.1:p.Phe577Val
ENST00000486164.5:c.559T>G
ENST00000488242.2:n.398T>G
NM_024757.4:c.2872T>G	NP_079033.4:p.Phe958Val
XM_005266105.3:c.2863T>G	XP_005266162.1:p.Phe955Val
XM_005266110.1:c.2779T>G	XP_005266167.1:p.Phe927Val
XM_006717288.2:c.2854T>G	XP_006717351.1:p.Phe952Val
XM_011519021.1:c.2881T>G	XP_011517323.1:p.Phe961Val
XM_011519022.1:c.2878T>G	XP_011517324.1:p.Phe960Val
XM_011519023.1:c.2860T>G	XP_011517325.1:p.Phe954Val
XM_011519024.1:c.2803T>G	XP_011517326.1:p.Phe935Val
XM_011519025.1:c.2779T>G	XP_011517327.1:p.Phe927Val
XM_011519026.1:c.2737T>G	XP_011517328.1:p.Phe913Val
XM_011519029.1:c.1303T>G	XP_011517331.1:p.Phe435Val
XM_011519030.1:c.655T>G	XP_011517332.1:p.Phe219Val
XM_011519031.1:c.442T>G	XP_011517333.1:p.Phe148Val
XM_011519032.1:c.442T>G	XP_011517334.1:p.Phe148Val
XM_011519033.1:c.2716T>G	XP_011517335.1:p.Phe906Val
NM_001354263.1:c.2851T>G	NP_001341192.1:p.Phe951Val
XM_005266105.5:c.2863T>G	XP_005266162.1:p.Phe955Val
XM_011519021.3:c.2881T>G	XP_011517323.1:p.Phe961Val
XM_011519022.3:c.2878T>G	XP_011517324.1:p.Phe960Val
XM_011519023.3:c.2860T>G	XP_011517325.1:p.Phe954Val
XM_011519029.3:c.1303T>G	XP_011517331.1:p.Phe435Val
XM_011519030.3:c.655T>G	XP_011517332.1:p.Phe219Val
XM_017015134.1:c.2857T>G	XP_016870623.1:p.Phe953Val
XM_017015136.2:c.2773T>G	XP_016870625.1:p.Phe925Val
XM_017015137.1:c.2758T>G	XP_016870626.1:p.Phe920Val
XM_017015138.1:c.2758T>G	XP_016870627.1:p.Phe920Val
XM_024447674.1:c.2701T>G	XP_024303442.1:p.Phe901Val
XM_024447675.1:c.2635T>G	XP_024303443.1:p.Phe879Val
XM_024447676.1:c.1996T>G	XP_024303444.1:p.Phe666Val
XM_024447677.1:c.1996T>G	XP_024303445.1:p.Phe666Val
XM_024447680.1:c.2614T>G	XP_024303448.1:p.Phe872Val
NM_024757.5:c.2872T>G MANE Select	NP_079033.4:p.Phe958Val
NM_001354263.2:c.2851T>G	NP_001341192.1:p.Phe951Val