Canonical Allele Identifier: CA375789004

Gene: EHMT1

Linked Data

• gnomAD v4: 9-137800964-G-A
• MyVariant Identifiers: chr9:g.140695416G>A (hg19) ; chr9:g.137800964G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800964G>A , CM000671.2:g.137800964G>A	GRCh38
NC_000009.11:g.140695416G>A , CM000671.1:g.140695416G>A	GRCh37
NC_000009.10:g.139815237G>A	NCBI36
NG_011776.1:g.186973G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2692G>A MANE Select	ENSP00000417980.1:p.Asp898Asn
ENST00000636027.1:c.2578G>A	ENSP00000489961.1:p.Asp860Asn
ENST00000637161.1:c.2599G>A	ENSP00000490328.1:p.Asp867Asn
ENST00000637261.1:c.2732G>A	ENSP00000490815.1:n.2732G>A
ENST00000637891.1:c.586G>A	ENSP00000490907.1:p.Asp196Asn
ENST00000637949.1:c.370G>A	ENSP00000489786.1:p.Asp124Asn
ENST00000460843.5:c.2692G>A	ENSP00000417980.1:p.Asp898Asn
ENST00000462942.3:c.1549G>A	ENSP00000436107.1:p.Asp517Asn
ENST00000482340.5:c.262G>A	ENSP00000486748.1:p.Asp88Asn
ENST00000486164.5:c.270G>A
ENST00000488242.2:n.218G>A
ENST00000493484.5:c.262G>A	ENSP00000486503.1:p.Asp88Asn
NM_024757.4:c.2692G>A	NP_079033.4:p.Asp898Asn
XM_005266105.3:c.2683G>A	XP_005266162.1:p.Asp895Asn
XM_005266110.1:c.2599G>A	XP_005266167.1:p.Asp867Asn
XM_006717288.2:c.2674G>A	XP_006717351.1:p.Asp892Asn
XM_011519021.1:c.2701G>A	XP_011517323.1:p.Asp901Asn
XM_011519022.1:c.2698G>A	XP_011517324.1:p.Asp900Asn
XM_011519023.1:c.2680G>A	XP_011517325.1:p.Asp894Asn
XM_011519024.1:c.2623G>A	XP_011517326.1:p.Asp875Asn
XM_011519025.1:c.2599G>A	XP_011517327.1:p.Asp867Asn
XM_011519026.1:c.2557G>A	XP_011517328.1:p.Asp853Asn
XM_011519027.1:c.2701G>A	XP_011517329.1:p.Asp901Asn
XM_011519029.1:c.1123G>A	XP_011517331.1:p.Asp375Asn
XM_011519030.1:c.475G>A	XP_011517332.1:p.Asp159Asn
XM_011519031.1:c.262G>A	XP_011517333.1:p.Asp88Asn
XM_011519032.1:c.262G>A	XP_011517334.1:p.Asp88Asn
XM_011519033.1:c.2536G>A	XP_011517335.1:p.Asp846Asn
NM_001354263.1:c.2671G>A	NP_001341192.1:p.Asp891Asn
XM_005266105.5:c.2683G>A	XP_005266162.1:p.Asp895Asn
XM_011519021.3:c.2701G>A	XP_011517323.1:p.Asp901Asn
XM_011519022.3:c.2698G>A	XP_011517324.1:p.Asp900Asn
XM_011519023.3:c.2680G>A	XP_011517325.1:p.Asp894Asn
XM_011519029.3:c.1123G>A	XP_011517331.1:p.Asp375Asn
XM_011519030.3:c.475G>A	XP_011517332.1:p.Asp159Asn
XM_017015134.1:c.2677G>A	XP_016870623.1:p.Asp893Asn
XM_017015136.2:c.2593G>A	XP_016870625.1:p.Asp865Asn
XM_017015137.1:c.2578G>A	XP_016870626.1:p.Asp860Asn
XM_017015138.1:c.2578G>A	XP_016870627.1:p.Asp860Asn
XM_024447674.1:c.2521G>A	XP_024303442.1:p.Asp841Asn
XM_024447675.1:c.2455G>A	XP_024303443.1:p.Asp819Asn
XM_024447676.1:c.1816G>A	XP_024303444.1:p.Asp606Asn
XM_024447677.1:c.1816G>A	XP_024303445.1:p.Asp606Asn
XM_024447678.1:c.2599G>A	XP_024303446.1:p.Asp867Asn
XM_024447680.1:c.2434G>A	XP_024303448.1:p.Asp812Asn
NM_024757.5:c.2692G>A MANE Select	NP_079033.4:p.Asp898Asn
NM_001354263.2:c.2671G>A	NP_001341192.1:p.Asp891Asn