Canonical Allele Identifier: CA375789038

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695424C>G (hg19) ; chr9:g.137800972C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800972C>G , CM000671.2:g.137800972C>G	GRCh38
NC_000009.11:g.140695424C>G , CM000671.1:g.140695424C>G	GRCh37
NC_000009.10:g.139815245C>G	NCBI36
NG_011776.1:g.186981C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2700C>G MANE Select	ENSP00000417980.1:p.Asn900Lys
ENST00000636027.1:c.2586C>G	ENSP00000489961.1:p.Asn862Lys
ENST00000637161.1:c.2607C>G	ENSP00000490328.1:p.Asn869Lys
ENST00000637261.1:c.2740C>G	ENSP00000490815.1:n.2740C>G
ENST00000637891.1:c.594C>G	ENSP00000490907.1:p.Asn198Lys
ENST00000637949.1:c.378C>G	ENSP00000489786.1:p.Asn126Lys
ENST00000460843.5:c.2700C>G	ENSP00000417980.1:p.Asn900Lys
ENST00000462942.3:c.1557C>G	ENSP00000436107.1:p.Asn519Lys
ENST00000482340.5:c.270C>G	ENSP00000486748.1:p.Asn90Lys
ENST00000486164.5:c.278C>G
ENST00000488242.2:n.226C>G
ENST00000493484.5:c.270C>G	ENSP00000486503.1:p.Asn90Lys
NM_024757.4:c.2700C>G	NP_079033.4:p.Asn900Lys
XM_005266105.3:c.2691C>G	XP_005266162.1:p.Asn897Lys
XM_005266110.1:c.2607C>G	XP_005266167.1:p.Asn869Lys
XM_006717288.2:c.2682C>G	XP_006717351.1:p.Asn894Lys
XM_011519021.1:c.2709C>G	XP_011517323.1:p.Asn903Lys
XM_011519022.1:c.2706C>G	XP_011517324.1:p.Asn902Lys
XM_011519023.1:c.2688C>G	XP_011517325.1:p.Asn896Lys
XM_011519024.1:c.2631C>G	XP_011517326.1:p.Asn877Lys
XM_011519025.1:c.2607C>G	XP_011517327.1:p.Asn869Lys
XM_011519026.1:c.2565C>G	XP_011517328.1:p.Asn855Lys
XM_011519027.1:c.2709C>G	XP_011517329.1:p.Asn903Lys
XM_011519029.1:c.1131C>G	XP_011517331.1:p.Asn377Lys
XM_011519030.1:c.483C>G	XP_011517332.1:p.Asn161Lys
XM_011519031.1:c.270C>G	XP_011517333.1:p.Asn90Lys
XM_011519032.1:c.270C>G	XP_011517334.1:p.Asn90Lys
XM_011519033.1:c.2544C>G	XP_011517335.1:p.Asn848Lys
NM_001354263.1:c.2679C>G	NP_001341192.1:p.Asn893Lys
XM_005266105.5:c.2691C>G	XP_005266162.1:p.Asn897Lys
XM_011519021.3:c.2709C>G	XP_011517323.1:p.Asn903Lys
XM_011519022.3:c.2706C>G	XP_011517324.1:p.Asn902Lys
XM_011519023.3:c.2688C>G	XP_011517325.1:p.Asn896Lys
XM_011519029.3:c.1131C>G	XP_011517331.1:p.Asn377Lys
XM_011519030.3:c.483C>G	XP_011517332.1:p.Asn161Lys
XM_017015134.1:c.2685C>G	XP_016870623.1:p.Asn895Lys
XM_017015136.2:c.2601C>G	XP_016870625.1:p.Asn867Lys
XM_017015137.1:c.2586C>G	XP_016870626.1:p.Asn862Lys
XM_017015138.1:c.2586C>G	XP_016870627.1:p.Asn862Lys
XM_024447674.1:c.2529C>G	XP_024303442.1:p.Asn843Lys
XM_024447675.1:c.2463C>G	XP_024303443.1:p.Asn821Lys
XM_024447676.1:c.1824C>G	XP_024303444.1:p.Asn608Lys
XM_024447677.1:c.1824C>G	XP_024303445.1:p.Asn608Lys
XM_024447678.1:c.2607C>G	XP_024303446.1:p.Asn869Lys
XM_024447680.1:c.2442C>G	XP_024303448.1:p.Asn814Lys
NM_024757.5:c.2700C>G MANE Select	NP_079033.4:p.Asn900Lys
NM_001354263.2:c.2679C>G	NP_001341192.1:p.Asn893Lys