Canonical Allele Identifier: CA375793456

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707535A>T (hg19) ; chr9:g.137813083A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813083A>T , CM000671.2:g.137813083A>T	GRCh38
NC_000009.11:g.140707535A>T , CM000671.1:g.140707535A>T	GRCh37
NC_000009.10:g.139827356A>T	NCBI36
NG_011776.1:g.199092A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2945A>T MANE Select	ENSP00000417980.1:p.Asn982Ile
ENST00000636027.1:c.2831A>T	ENSP00000489961.1:p.Asn944Ile
ENST00000637161.1:c.2852A>T	ENSP00000490328.1:p.Asn951Ile
ENST00000637261.1:c.2985A>T	ENSP00000490815.1:n.2985A>T
ENST00000637891.1:c.839A>T	ENSP00000490907.1:p.Asn280Ile
ENST00000460843.5:c.2945A>T	ENSP00000417980.1:p.Asn982Ile
ENST00000462942.3:c.1802A>T	ENSP00000436107.1:p.Asn601Ile
ENST00000486164.5:c.632A>T
ENST00000488242.2:n.471A>T
NM_024757.4:c.2945A>T	NP_079033.4:p.Asn982Ile
XM_005266105.3:c.2936A>T	XP_005266162.1:p.Asn979Ile
XM_005266110.1:c.2852A>T	XP_005266167.1:p.Asn951Ile
XM_006717288.2:c.2927A>T	XP_006717351.1:p.Asn976Ile
XM_011519021.1:c.2954A>T	XP_011517323.1:p.Asn985Ile
XM_011519022.1:c.2951A>T	XP_011517324.1:p.Asn984Ile
XM_011519023.1:c.2933A>T	XP_011517325.1:p.Asn978Ile
XM_011519024.1:c.2876A>T	XP_011517326.1:p.Asn959Ile
XM_011519025.1:c.2852A>T	XP_011517327.1:p.Asn951Ile
XM_011519026.1:c.2810A>T	XP_011517328.1:p.Asn937Ile
XM_011519029.1:c.1376A>T	XP_011517331.1:p.Asn459Ile
XM_011519030.1:c.728A>T	XP_011517332.1:p.Asn243Ile
XM_011519031.1:c.515A>T	XP_011517333.1:p.Asn172Ile
XM_011519032.1:c.515A>T	XP_011517334.1:p.Asn172Ile
XM_011519033.1:c.2789A>T	XP_011517335.1:p.Asn930Ile
NM_001354263.1:c.2924A>T	NP_001341192.1:p.Asn975Ile
XM_005266105.5:c.2936A>T	XP_005266162.1:p.Asn979Ile
XM_011519021.3:c.2954A>T	XP_011517323.1:p.Asn985Ile
XM_011519022.3:c.2951A>T	XP_011517324.1:p.Asn984Ile
XM_011519023.3:c.2933A>T	XP_011517325.1:p.Asn978Ile
XM_011519029.3:c.1376A>T	XP_011517331.1:p.Asn459Ile
XM_011519030.3:c.728A>T	XP_011517332.1:p.Asn243Ile
XM_017015134.1:c.2930A>T	XP_016870623.1:p.Asn977Ile
XM_017015136.2:c.2846A>T	XP_016870625.1:p.Asn949Ile
XM_017015137.1:c.2831A>T	XP_016870626.1:p.Asn944Ile
XM_017015138.1:c.2831A>T	XP_016870627.1:p.Asn944Ile
XM_024447674.1:c.2774A>T	XP_024303442.1:p.Asn925Ile
XM_024447675.1:c.2708A>T	XP_024303443.1:p.Asn903Ile
XM_024447676.1:c.2069A>T	XP_024303444.1:p.Asn690Ile
XM_024447677.1:c.2069A>T	XP_024303445.1:p.Asn690Ile
XM_024447680.1:c.2687A>T	XP_024303448.1:p.Asn896Ile
NM_024757.5:c.2945A>T MANE Select	NP_079033.4:p.Asn982Ile
NM_001354263.2:c.2924A>T	NP_001341192.1:p.Asn975Ile