Canonical Allele Identifier: CA375793672

Gene: EHMT1

Linked Data

• dbSNP Id: rs1462693300
• MyVariant Identifiers: chr9:g.140707589C>G (hg19) ; chr9:g.137813137C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813137C>G , CM000671.2:g.137813137C>G	GRCh38
NC_000009.11:g.140707589C>G , CM000671.1:g.140707589C>G	GRCh37
NC_000009.10:g.139827410C>G	NCBI36
NG_011776.1:g.199146C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2999C>G MANE Select	ENSP00000417980.1:p.Pro1000Arg
ENST00000636027.1:c.2885C>G	ENSP00000489961.1:p.Pro962Arg
ENST00000637161.1:c.2906C>G	ENSP00000490328.1:p.Pro969Arg
ENST00000637261.1:c.3039C>G	ENSP00000490815.1:n.3039C>G
ENST00000637891.1:c.893C>G	ENSP00000490907.1:p.Pro298Arg
ENST00000460843.5:c.2999C>G	ENSP00000417980.1:p.Pro1000Arg
ENST00000462942.3:c.1856C>G	ENSP00000436107.1:p.Pro619Arg
ENST00000486164.5:c.686C>G
ENST00000488242.2:n.525C>G
NM_024757.4:c.2999C>G	NP_079033.4:p.Pro1000Arg
XM_005266105.3:c.2990C>G	XP_005266162.1:p.Pro997Arg
XM_005266110.1:c.2906C>G	XP_005266167.1:p.Pro969Arg
XM_006717288.2:c.2981C>G	XP_006717351.1:p.Pro994Arg
XM_011519021.1:c.3008C>G	XP_011517323.1:p.Pro1003Arg
XM_011519022.1:c.3005C>G	XP_011517324.1:p.Pro1002Arg
XM_011519023.1:c.2987C>G	XP_011517325.1:p.Pro996Arg
XM_011519024.1:c.2930C>G	XP_011517326.1:p.Pro977Arg
XM_011519025.1:c.2906C>G	XP_011517327.1:p.Pro969Arg
XM_011519026.1:c.2864C>G	XP_011517328.1:p.Pro955Arg
XM_011519029.1:c.1430C>G	XP_011517331.1:p.Pro477Arg
XM_011519030.1:c.782C>G	XP_011517332.1:p.Pro261Arg
XM_011519031.1:c.569C>G	XP_011517333.1:p.Pro190Arg
XM_011519032.1:c.569C>G	XP_011517334.1:p.Pro190Arg
XM_011519033.1:c.2843C>G	XP_011517335.1:p.Pro948Arg
NM_001354263.1:c.2978C>G	NP_001341192.1:p.Pro993Arg
XM_005266105.5:c.2990C>G	XP_005266162.1:p.Pro997Arg
XM_011519021.3:c.3008C>G	XP_011517323.1:p.Pro1003Arg
XM_011519022.3:c.3005C>G	XP_011517324.1:p.Pro1002Arg
XM_011519023.3:c.2987C>G	XP_011517325.1:p.Pro996Arg
XM_011519029.3:c.1430C>G	XP_011517331.1:p.Pro477Arg
XM_011519030.3:c.782C>G	XP_011517332.1:p.Pro261Arg
XM_017015134.1:c.2984C>G	XP_016870623.1:p.Pro995Arg
XM_017015136.2:c.2900C>G	XP_016870625.1:p.Pro967Arg
XM_017015137.1:c.2885C>G	XP_016870626.1:p.Pro962Arg
XM_017015138.1:c.2885C>G	XP_016870627.1:p.Pro962Arg
XM_024447674.1:c.2828C>G	XP_024303442.1:p.Pro943Arg
XM_024447675.1:c.2762C>G	XP_024303443.1:p.Pro921Arg
XM_024447676.1:c.2123C>G	XP_024303444.1:p.Pro708Arg
XM_024447677.1:c.2123C>G	XP_024303445.1:p.Pro708Arg
XM_024447680.1:c.2741C>G	XP_024303448.1:p.Pro914Arg
NM_024757.5:c.2999C>G MANE Select	NP_079033.4:p.Pro1000Arg
NM_001354263.2:c.2978C>G	NP_001341192.1:p.Pro993Arg