Canonical Allele Identifier: CA468161109

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707620G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813168G>A , CM000671.2:g.137813168G>A	GRCh38
NC_000009.11:g.140707620G>A , CM000671.1:g.140707620G>A	GRCh37
NC_000009.10:g.139827441G>A	NCBI36
NG_011776.1:g.199177G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3030G>A MANE Select	ENSP00000417980.1:p.Val1010=
ENST00000636027.1:c.2916G>A	ENSP00000489961.1:p.Val972=
ENST00000637161.1:c.2937G>A	ENSP00000490328.1:p.Val979=
ENST00000637261.1:c.3070G>A	ENSP00000490815.1:n.3070G>A
ENST00000637891.1:c.924G>A	ENSP00000490907.1:p.Val308=
ENST00000460843.5:c.3030G>A	ENSP00000417980.1:p.Val1010=
ENST00000462942.3:c.1887G>A	ENSP00000436107.1:p.Val629=
ENST00000486164.5:c.717G>A
ENST00000488242.2:n.556G>A
NM_024757.4:c.3030G>A	NP_079033.4:p.Val1010=
XM_005266105.3:c.3021G>A	XP_005266162.1:p.Val1007=
XM_005266110.1:c.2937G>A	XP_005266167.1:p.Val979=
XM_006717288.2:c.3012G>A	XP_006717351.1:p.Val1004=
XM_011519021.1:c.3039G>A	XP_011517323.1:p.Val1013=
XM_011519022.1:c.3036G>A	XP_011517324.1:p.Val1012=
XM_011519023.1:c.3018G>A	XP_011517325.1:p.Val1006=
XM_011519024.1:c.2961G>A	XP_011517326.1:p.Val987=
XM_011519025.1:c.2937G>A	XP_011517327.1:p.Val979=
XM_011519026.1:c.2895G>A	XP_011517328.1:p.Val965=
XM_011519029.1:c.1461G>A	XP_011517331.1:p.Val487=
XM_011519030.1:c.813G>A	XP_011517332.1:p.Val271=
XM_011519031.1:c.600G>A	XP_011517333.1:p.Val200=
XM_011519032.1:c.600G>A	XP_011517334.1:p.Val200=
XM_011519033.1:c.2874G>A	XP_011517335.1:p.Val958=
NM_001354263.1:c.3009G>A	NP_001341192.1:p.Val1003=
XM_005266105.5:c.3021G>A	XP_005266162.1:p.Val1007=
XM_011519021.3:c.3039G>A	XP_011517323.1:p.Val1013=
XM_011519022.3:c.3036G>A	XP_011517324.1:p.Val1012=
XM_011519023.3:c.3018G>A	XP_011517325.1:p.Val1006=
XM_011519029.3:c.1461G>A	XP_011517331.1:p.Val487=
XM_011519030.3:c.813G>A	XP_011517332.1:p.Val271=
XM_017015134.1:c.3015G>A	XP_016870623.1:p.Val1005=
XM_017015136.2:c.2931G>A	XP_016870625.1:p.Val977=
XM_017015137.1:c.2916G>A	XP_016870626.1:p.Val972=
XM_017015138.1:c.2916G>A	XP_016870627.1:p.Val972=
XM_024447674.1:c.2859G>A	XP_024303442.1:p.Val953=
XM_024447675.1:c.2793G>A	XP_024303443.1:p.Val931=
XM_024447676.1:c.2154G>A	XP_024303444.1:p.Val718=
XM_024447677.1:c.2154G>A	XP_024303445.1:p.Val718=
XM_024447680.1:c.2772G>A	XP_024303448.1:p.Val924=
NM_024757.5:c.3030G>A MANE Select	NP_079033.4:p.Val1010=
NM_001354263.2:c.3009G>A	NP_001341192.1:p.Val1003=