Canonical Allele Identifier: CA468161048

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707515C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813063C>A , CM000671.2:g.137813063C>A	GRCh38
NC_000009.11:g.140707515C>A , CM000671.1:g.140707515C>A	GRCh37
NC_000009.10:g.139827336C>A	NCBI36
NG_011776.1:g.199072C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2925C>A MANE Select	ENSP00000417980.1:p.Pro975=
ENST00000636027.1:c.2811C>A	ENSP00000489961.1:p.Pro937=
ENST00000637161.1:c.2832C>A	ENSP00000490328.1:p.Pro944=
ENST00000637261.1:c.2965C>A	ENSP00000490815.1:n.2965C>A
ENST00000637891.1:c.819C>A	ENSP00000490907.1:p.Pro273=
ENST00000460843.5:c.2925C>A	ENSP00000417980.1:p.Pro975=
ENST00000462942.3:c.1782C>A	ENSP00000436107.1:p.Pro594=
ENST00000486164.5:c.612C>A
ENST00000488242.2:n.451C>A
NM_024757.4:c.2925C>A	NP_079033.4:p.Pro975=
XM_005266105.3:c.2916C>A	XP_005266162.1:p.Pro972=
XM_005266110.1:c.2832C>A	XP_005266167.1:p.Pro944=
XM_006717288.2:c.2907C>A	XP_006717351.1:p.Pro969=
XM_011519021.1:c.2934C>A	XP_011517323.1:p.Pro978=
XM_011519022.1:c.2931C>A	XP_011517324.1:p.Pro977=
XM_011519023.1:c.2913C>A	XP_011517325.1:p.Pro971=
XM_011519024.1:c.2856C>A	XP_011517326.1:p.Pro952=
XM_011519025.1:c.2832C>A	XP_011517327.1:p.Pro944=
XM_011519026.1:c.2790C>A	XP_011517328.1:p.Pro930=
XM_011519029.1:c.1356C>A	XP_011517331.1:p.Pro452=
XM_011519030.1:c.708C>A	XP_011517332.1:p.Pro236=
XM_011519031.1:c.495C>A	XP_011517333.1:p.Pro165=
XM_011519032.1:c.495C>A	XP_011517334.1:p.Pro165=
XM_011519033.1:c.2769C>A	XP_011517335.1:p.Pro923=
NM_001354263.1:c.2904C>A	NP_001341192.1:p.Pro968=
XM_005266105.5:c.2916C>A	XP_005266162.1:p.Pro972=
XM_011519021.3:c.2934C>A	XP_011517323.1:p.Pro978=
XM_011519022.3:c.2931C>A	XP_011517324.1:p.Pro977=
XM_011519023.3:c.2913C>A	XP_011517325.1:p.Pro971=
XM_011519029.3:c.1356C>A	XP_011517331.1:p.Pro452=
XM_011519030.3:c.708C>A	XP_011517332.1:p.Pro236=
XM_017015134.1:c.2910C>A	XP_016870623.1:p.Pro970=
XM_017015136.2:c.2826C>A	XP_016870625.1:p.Pro942=
XM_017015137.1:c.2811C>A	XP_016870626.1:p.Pro937=
XM_017015138.1:c.2811C>A	XP_016870627.1:p.Pro937=
XM_024447674.1:c.2754C>A	XP_024303442.1:p.Pro918=
XM_024447675.1:c.2688C>A	XP_024303443.1:p.Pro896=
XM_024447676.1:c.2049C>A	XP_024303444.1:p.Pro683=
XM_024447677.1:c.2049C>A	XP_024303445.1:p.Pro683=
XM_024447680.1:c.2667C>A	XP_024303448.1:p.Pro889=
NM_024757.5:c.2925C>A MANE Select	NP_079033.4:p.Pro975=
NM_001354263.2:c.2904C>A	NP_001341192.1:p.Pro968=