Canonical Allele Identifier: CA468161107

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707617A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813165A>C , CM000671.2:g.137813165A>C	GRCh38
NC_000009.11:g.140707617A>C , CM000671.1:g.140707617A>C	GRCh37
NC_000009.10:g.139827438A>C	NCBI36
NG_011776.1:g.199174A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3027A>C MANE Select	ENSP00000417980.1:p.Ile1009=
ENST00000636027.1:c.2913A>C	ENSP00000489961.1:p.Ile971=
ENST00000637161.1:c.2934A>C	ENSP00000490328.1:p.Ile978=
ENST00000637261.1:c.3067A>C	ENSP00000490815.1:n.3067A>C
ENST00000637891.1:c.921A>C	ENSP00000490907.1:p.Ile307=
ENST00000460843.5:c.3027A>C	ENSP00000417980.1:p.Ile1009=
ENST00000462942.3:c.1884A>C	ENSP00000436107.1:p.Ile628=
ENST00000486164.5:c.714A>C
ENST00000488242.2:n.553A>C
NM_024757.4:c.3027A>C	NP_079033.4:p.Ile1009=
XM_005266105.3:c.3018A>C	XP_005266162.1:p.Ile1006=
XM_005266110.1:c.2934A>C	XP_005266167.1:p.Ile978=
XM_006717288.2:c.3009A>C	XP_006717351.1:p.Ile1003=
XM_011519021.1:c.3036A>C	XP_011517323.1:p.Ile1012=
XM_011519022.1:c.3033A>C	XP_011517324.1:p.Ile1011=
XM_011519023.1:c.3015A>C	XP_011517325.1:p.Ile1005=
XM_011519024.1:c.2958A>C	XP_011517326.1:p.Ile986=
XM_011519025.1:c.2934A>C	XP_011517327.1:p.Ile978=
XM_011519026.1:c.2892A>C	XP_011517328.1:p.Ile964=
XM_011519029.1:c.1458A>C	XP_011517331.1:p.Ile486=
XM_011519030.1:c.810A>C	XP_011517332.1:p.Ile270=
XM_011519031.1:c.597A>C	XP_011517333.1:p.Ile199=
XM_011519032.1:c.597A>C	XP_011517334.1:p.Ile199=
XM_011519033.1:c.2871A>C	XP_011517335.1:p.Ile957=
NM_001354263.1:c.3006A>C	NP_001341192.1:p.Ile1002=
XM_005266105.5:c.3018A>C	XP_005266162.1:p.Ile1006=
XM_011519021.3:c.3036A>C	XP_011517323.1:p.Ile1012=
XM_011519022.3:c.3033A>C	XP_011517324.1:p.Ile1011=
XM_011519023.3:c.3015A>C	XP_011517325.1:p.Ile1005=
XM_011519029.3:c.1458A>C	XP_011517331.1:p.Ile486=
XM_011519030.3:c.810A>C	XP_011517332.1:p.Ile270=
XM_017015134.1:c.3012A>C	XP_016870623.1:p.Ile1004=
XM_017015136.2:c.2928A>C	XP_016870625.1:p.Ile976=
XM_017015137.1:c.2913A>C	XP_016870626.1:p.Ile971=
XM_017015138.1:c.2913A>C	XP_016870627.1:p.Ile971=
XM_024447674.1:c.2856A>C	XP_024303442.1:p.Ile952=
XM_024447675.1:c.2790A>C	XP_024303443.1:p.Ile930=
XM_024447676.1:c.2151A>C	XP_024303444.1:p.Ile717=
XM_024447677.1:c.2151A>C	XP_024303445.1:p.Ile717=
XM_024447680.1:c.2769A>C	XP_024303448.1:p.Ile923=
NM_024757.5:c.3027A>C MANE Select	NP_079033.4:p.Ile1009=
NM_001354263.2:c.3006A>C	NP_001341192.1:p.Ile1002=