Canonical Allele Identifier: CA375793316

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707495A>T (hg19) ; chr9:g.137813043A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813043A>T , CM000671.2:g.137813043A>T	GRCh38
NC_000009.11:g.140707495A>T , CM000671.1:g.140707495A>T	GRCh37
NC_000009.10:g.139827316A>T	NCBI36
NG_011776.1:g.199052A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2905A>T MANE Select	ENSP00000417980.1:p.Asn969Tyr
ENST00000636027.1:c.2791A>T	ENSP00000489961.1:p.Asn931Tyr
ENST00000637161.1:c.2812A>T	ENSP00000490328.1:p.Asn938Tyr
ENST00000637261.1:c.2945A>T	ENSP00000490815.1:n.2945A>T
ENST00000637891.1:c.799A>T	ENSP00000490907.1:p.Asn267Tyr
ENST00000460843.5:c.2905A>T	ENSP00000417980.1:p.Asn969Tyr
ENST00000462942.3:c.1762A>T	ENSP00000436107.1:p.Asn588Tyr
ENST00000486164.5:c.592A>T
ENST00000488242.2:n.431A>T
NM_024757.4:c.2905A>T	NP_079033.4:p.Asn969Tyr
XM_005266105.3:c.2896A>T	XP_005266162.1:p.Asn966Tyr
XM_005266110.1:c.2812A>T	XP_005266167.1:p.Asn938Tyr
XM_006717288.2:c.2887A>T	XP_006717351.1:p.Asn963Tyr
XM_011519021.1:c.2914A>T	XP_011517323.1:p.Asn972Tyr
XM_011519022.1:c.2911A>T	XP_011517324.1:p.Asn971Tyr
XM_011519023.1:c.2893A>T	XP_011517325.1:p.Asn965Tyr
XM_011519024.1:c.2836A>T	XP_011517326.1:p.Asn946Tyr
XM_011519025.1:c.2812A>T	XP_011517327.1:p.Asn938Tyr
XM_011519026.1:c.2770A>T	XP_011517328.1:p.Asn924Tyr
XM_011519029.1:c.1336A>T	XP_011517331.1:p.Asn446Tyr
XM_011519030.1:c.688A>T	XP_011517332.1:p.Asn230Tyr
XM_011519031.1:c.475A>T	XP_011517333.1:p.Asn159Tyr
XM_011519032.1:c.475A>T	XP_011517334.1:p.Asn159Tyr
XM_011519033.1:c.2749A>T	XP_011517335.1:p.Asn917Tyr
NM_001354263.1:c.2884A>T	NP_001341192.1:p.Asn962Tyr
XM_005266105.5:c.2896A>T	XP_005266162.1:p.Asn966Tyr
XM_011519021.3:c.2914A>T	XP_011517323.1:p.Asn972Tyr
XM_011519022.3:c.2911A>T	XP_011517324.1:p.Asn971Tyr
XM_011519023.3:c.2893A>T	XP_011517325.1:p.Asn965Tyr
XM_011519029.3:c.1336A>T	XP_011517331.1:p.Asn446Tyr
XM_011519030.3:c.688A>T	XP_011517332.1:p.Asn230Tyr
XM_017015134.1:c.2890A>T	XP_016870623.1:p.Asn964Tyr
XM_017015136.2:c.2806A>T	XP_016870625.1:p.Asn936Tyr
XM_017015137.1:c.2791A>T	XP_016870626.1:p.Asn931Tyr
XM_017015138.1:c.2791A>T	XP_016870627.1:p.Asn931Tyr
XM_024447674.1:c.2734A>T	XP_024303442.1:p.Asn912Tyr
XM_024447675.1:c.2668A>T	XP_024303443.1:p.Asn890Tyr
XM_024447676.1:c.2029A>T	XP_024303444.1:p.Asn677Tyr
XM_024447677.1:c.2029A>T	XP_024303445.1:p.Asn677Tyr
XM_024447680.1:c.2647A>T	XP_024303448.1:p.Asn883Tyr
NM_024757.5:c.2905A>T MANE Select	NP_079033.4:p.Asn969Tyr
NM_001354263.2:c.2884A>T	NP_001341192.1:p.Asn962Tyr