Canonical Allele Identifier: CA375793472

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707540C>A (hg19) ; chr9:g.137813088C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813088C>A , CM000671.2:g.137813088C>A	GRCh38
NC_000009.11:g.140707540C>A , CM000671.1:g.140707540C>A	GRCh37
NC_000009.10:g.139827361C>A	NCBI36
NG_011776.1:g.199097C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2950C>A MANE Select	ENSP00000417980.1:p.Gln984Lys
ENST00000636027.1:c.2836C>A	ENSP00000489961.1:p.Gln946Lys
ENST00000637161.1:c.2857C>A	ENSP00000490328.1:p.Gln953Lys
ENST00000637261.1:c.2990C>A	ENSP00000490815.1:n.2990C>A
ENST00000637891.1:c.844C>A	ENSP00000490907.1:p.Gln282Lys
ENST00000460843.5:c.2950C>A	ENSP00000417980.1:p.Gln984Lys
ENST00000462942.3:c.1807C>A	ENSP00000436107.1:p.Gln603Lys
ENST00000486164.5:c.637C>A
ENST00000488242.2:n.476C>A
NM_024757.4:c.2950C>A	NP_079033.4:p.Gln984Lys
XM_005266105.3:c.2941C>A	XP_005266162.1:p.Gln981Lys
XM_005266110.1:c.2857C>A	XP_005266167.1:p.Gln953Lys
XM_006717288.2:c.2932C>A	XP_006717351.1:p.Gln978Lys
XM_011519021.1:c.2959C>A	XP_011517323.1:p.Gln987Lys
XM_011519022.1:c.2956C>A	XP_011517324.1:p.Gln986Lys
XM_011519023.1:c.2938C>A	XP_011517325.1:p.Gln980Lys
XM_011519024.1:c.2881C>A	XP_011517326.1:p.Gln961Lys
XM_011519025.1:c.2857C>A	XP_011517327.1:p.Gln953Lys
XM_011519026.1:c.2815C>A	XP_011517328.1:p.Gln939Lys
XM_011519029.1:c.1381C>A	XP_011517331.1:p.Gln461Lys
XM_011519030.1:c.733C>A	XP_011517332.1:p.Gln245Lys
XM_011519031.1:c.520C>A	XP_011517333.1:p.Gln174Lys
XM_011519032.1:c.520C>A	XP_011517334.1:p.Gln174Lys
XM_011519033.1:c.2794C>A	XP_011517335.1:p.Gln932Lys
NM_001354263.1:c.2929C>A	NP_001341192.1:p.Gln977Lys
XM_005266105.5:c.2941C>A	XP_005266162.1:p.Gln981Lys
XM_011519021.3:c.2959C>A	XP_011517323.1:p.Gln987Lys
XM_011519022.3:c.2956C>A	XP_011517324.1:p.Gln986Lys
XM_011519023.3:c.2938C>A	XP_011517325.1:p.Gln980Lys
XM_011519029.3:c.1381C>A	XP_011517331.1:p.Gln461Lys
XM_011519030.3:c.733C>A	XP_011517332.1:p.Gln245Lys
XM_017015134.1:c.2935C>A	XP_016870623.1:p.Gln979Lys
XM_017015136.2:c.2851C>A	XP_016870625.1:p.Gln951Lys
XM_017015137.1:c.2836C>A	XP_016870626.1:p.Gln946Lys
XM_017015138.1:c.2836C>A	XP_016870627.1:p.Gln946Lys
XM_024447674.1:c.2779C>A	XP_024303442.1:p.Gln927Lys
XM_024447675.1:c.2713C>A	XP_024303443.1:p.Gln905Lys
XM_024447676.1:c.2074C>A	XP_024303444.1:p.Gln692Lys
XM_024447677.1:c.2074C>A	XP_024303445.1:p.Gln692Lys
XM_024447680.1:c.2692C>A	XP_024303448.1:p.Gln898Lys
NM_024757.5:c.2950C>A MANE Select	NP_079033.4:p.Gln984Lys
NM_001354263.2:c.2929C>A	NP_001341192.1:p.Gln977Lys