Canonical Allele Identifier: CA375793458

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707536C>A (hg19) ; chr9:g.137813084C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813084C>A , CM000671.2:g.137813084C>A	GRCh38
NC_000009.11:g.140707536C>A , CM000671.1:g.140707536C>A	GRCh37
NC_000009.10:g.139827357C>A	NCBI36
NG_011776.1:g.199093C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2946C>A MANE Select	ENSP00000417980.1:p.Asn982Lys
ENST00000636027.1:c.2832C>A	ENSP00000489961.1:p.Asn944Lys
ENST00000637161.1:c.2853C>A	ENSP00000490328.1:p.Asn951Lys
ENST00000637261.1:c.2986C>A	ENSP00000490815.1:n.2986C>A
ENST00000637891.1:c.840C>A	ENSP00000490907.1:p.Asn280Lys
ENST00000460843.5:c.2946C>A	ENSP00000417980.1:p.Asn982Lys
ENST00000462942.3:c.1803C>A	ENSP00000436107.1:p.Asn601Lys
ENST00000486164.5:c.633C>A
ENST00000488242.2:n.472C>A
NM_024757.4:c.2946C>A	NP_079033.4:p.Asn982Lys
XM_005266105.3:c.2937C>A	XP_005266162.1:p.Asn979Lys
XM_005266110.1:c.2853C>A	XP_005266167.1:p.Asn951Lys
XM_006717288.2:c.2928C>A	XP_006717351.1:p.Asn976Lys
XM_011519021.1:c.2955C>A	XP_011517323.1:p.Asn985Lys
XM_011519022.1:c.2952C>A	XP_011517324.1:p.Asn984Lys
XM_011519023.1:c.2934C>A	XP_011517325.1:p.Asn978Lys
XM_011519024.1:c.2877C>A	XP_011517326.1:p.Asn959Lys
XM_011519025.1:c.2853C>A	XP_011517327.1:p.Asn951Lys
XM_011519026.1:c.2811C>A	XP_011517328.1:p.Asn937Lys
XM_011519029.1:c.1377C>A	XP_011517331.1:p.Asn459Lys
XM_011519030.1:c.729C>A	XP_011517332.1:p.Asn243Lys
XM_011519031.1:c.516C>A	XP_011517333.1:p.Asn172Lys
XM_011519032.1:c.516C>A	XP_011517334.1:p.Asn172Lys
XM_011519033.1:c.2790C>A	XP_011517335.1:p.Asn930Lys
NM_001354263.1:c.2925C>A	NP_001341192.1:p.Asn975Lys
XM_005266105.5:c.2937C>A	XP_005266162.1:p.Asn979Lys
XM_011519021.3:c.2955C>A	XP_011517323.1:p.Asn985Lys
XM_011519022.3:c.2952C>A	XP_011517324.1:p.Asn984Lys
XM_011519023.3:c.2934C>A	XP_011517325.1:p.Asn978Lys
XM_011519029.3:c.1377C>A	XP_011517331.1:p.Asn459Lys
XM_011519030.3:c.729C>A	XP_011517332.1:p.Asn243Lys
XM_017015134.1:c.2931C>A	XP_016870623.1:p.Asn977Lys
XM_017015136.2:c.2847C>A	XP_016870625.1:p.Asn949Lys
XM_017015137.1:c.2832C>A	XP_016870626.1:p.Asn944Lys
XM_017015138.1:c.2832C>A	XP_016870627.1:p.Asn944Lys
XM_024447674.1:c.2775C>A	XP_024303442.1:p.Asn925Lys
XM_024447675.1:c.2709C>A	XP_024303443.1:p.Asn903Lys
XM_024447676.1:c.2070C>A	XP_024303444.1:p.Asn690Lys
XM_024447677.1:c.2070C>A	XP_024303445.1:p.Asn690Lys
XM_024447680.1:c.2688C>A	XP_024303448.1:p.Asn896Lys
NM_024757.5:c.2946C>A MANE Select	NP_079033.4:p.Asn982Lys
NM_001354263.2:c.2925C>A	NP_001341192.1:p.Asn975Lys