Canonical Allele Identifier: CA375793375

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707514C>G (hg19) ; chr9:g.137813062C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813062C>G , CM000671.2:g.137813062C>G	GRCh38
NC_000009.11:g.140707514C>G , CM000671.1:g.140707514C>G	GRCh37
NC_000009.10:g.139827335C>G	NCBI36
NG_011776.1:g.199071C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2924C>G MANE Select	ENSP00000417980.1:p.Pro975Arg
ENST00000636027.1:c.2810C>G	ENSP00000489961.1:p.Pro937Arg
ENST00000637161.1:c.2831C>G	ENSP00000490328.1:p.Pro944Arg
ENST00000637261.1:c.2964C>G	ENSP00000490815.1:n.2964C>G
ENST00000637891.1:c.818C>G	ENSP00000490907.1:p.Pro273Arg
ENST00000460843.5:c.2924C>G	ENSP00000417980.1:p.Pro975Arg
ENST00000462942.3:c.1781C>G	ENSP00000436107.1:p.Pro594Arg
ENST00000486164.5:c.611C>G
ENST00000488242.2:n.450C>G
NM_024757.4:c.2924C>G	NP_079033.4:p.Pro975Arg
XM_005266105.3:c.2915C>G	XP_005266162.1:p.Pro972Arg
XM_005266110.1:c.2831C>G	XP_005266167.1:p.Pro944Arg
XM_006717288.2:c.2906C>G	XP_006717351.1:p.Pro969Arg
XM_011519021.1:c.2933C>G	XP_011517323.1:p.Pro978Arg
XM_011519022.1:c.2930C>G	XP_011517324.1:p.Pro977Arg
XM_011519023.1:c.2912C>G	XP_011517325.1:p.Pro971Arg
XM_011519024.1:c.2855C>G	XP_011517326.1:p.Pro952Arg
XM_011519025.1:c.2831C>G	XP_011517327.1:p.Pro944Arg
XM_011519026.1:c.2789C>G	XP_011517328.1:p.Pro930Arg
XM_011519029.1:c.1355C>G	XP_011517331.1:p.Pro452Arg
XM_011519030.1:c.707C>G	XP_011517332.1:p.Pro236Arg
XM_011519031.1:c.494C>G	XP_011517333.1:p.Pro165Arg
XM_011519032.1:c.494C>G	XP_011517334.1:p.Pro165Arg
XM_011519033.1:c.2768C>G	XP_011517335.1:p.Pro923Arg
NM_001354263.1:c.2903C>G	NP_001341192.1:p.Pro968Arg
XM_005266105.5:c.2915C>G	XP_005266162.1:p.Pro972Arg
XM_011519021.3:c.2933C>G	XP_011517323.1:p.Pro978Arg
XM_011519022.3:c.2930C>G	XP_011517324.1:p.Pro977Arg
XM_011519023.3:c.2912C>G	XP_011517325.1:p.Pro971Arg
XM_011519029.3:c.1355C>G	XP_011517331.1:p.Pro452Arg
XM_011519030.3:c.707C>G	XP_011517332.1:p.Pro236Arg
XM_017015134.1:c.2909C>G	XP_016870623.1:p.Pro970Arg
XM_017015136.2:c.2825C>G	XP_016870625.1:p.Pro942Arg
XM_017015137.1:c.2810C>G	XP_016870626.1:p.Pro937Arg
XM_017015138.1:c.2810C>G	XP_016870627.1:p.Pro937Arg
XM_024447674.1:c.2753C>G	XP_024303442.1:p.Pro918Arg
XM_024447675.1:c.2687C>G	XP_024303443.1:p.Pro896Arg
XM_024447676.1:c.2048C>G	XP_024303444.1:p.Pro683Arg
XM_024447677.1:c.2048C>G	XP_024303445.1:p.Pro683Arg
XM_024447680.1:c.2666C>G	XP_024303448.1:p.Pro889Arg
NM_024757.5:c.2924C>G MANE Select	NP_079033.4:p.Pro975Arg
NM_001354263.2:c.2903C>G	NP_001341192.1:p.Pro968Arg