Canonical Allele Identifier: CA467877667

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695415T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800963T>C , CM000671.2:g.137800963T>C	GRCh38
NC_000009.11:g.140695415T>C , CM000671.1:g.140695415T>C	GRCh37
NC_000009.10:g.139815236T>C	NCBI36
NG_011776.1:g.186972T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2691T>C MANE Select	ENSP00000417980.1:p.Ser897=
ENST00000636027.1:c.2577T>C	ENSP00000489961.1:p.Ser859=
ENST00000637161.1:c.2598T>C	ENSP00000490328.1:p.Ser866=
ENST00000637261.1:c.2731T>C	ENSP00000490815.1:n.2731T>C
ENST00000637891.1:c.585T>C	ENSP00000490907.1:p.Ser195=
ENST00000637949.1:c.369T>C	ENSP00000489786.1:p.Ser123=
ENST00000460843.5:c.2691T>C	ENSP00000417980.1:p.Ser897=
ENST00000462942.3:c.1548T>C	ENSP00000436107.1:p.Ser516=
ENST00000482340.5:c.261T>C	ENSP00000486748.1:p.Ser87=
ENST00000486164.5:c.269T>C
ENST00000488242.2:n.217T>C
ENST00000493484.5:c.261T>C	ENSP00000486503.1:p.Ser87=
NM_024757.4:c.2691T>C	NP_079033.4:p.Ser897=
XM_005266105.3:c.2682T>C	XP_005266162.1:p.Ser894=
XM_005266110.1:c.2598T>C	XP_005266167.1:p.Ser866=
XM_006717288.2:c.2673T>C	XP_006717351.1:p.Ser891=
XM_011519021.1:c.2700T>C	XP_011517323.1:p.Ser900=
XM_011519022.1:c.2697T>C	XP_011517324.1:p.Ser899=
XM_011519023.1:c.2679T>C	XP_011517325.1:p.Ser893=
XM_011519024.1:c.2622T>C	XP_011517326.1:p.Ser874=
XM_011519025.1:c.2598T>C	XP_011517327.1:p.Ser866=
XM_011519026.1:c.2556T>C	XP_011517328.1:p.Ser852=
XM_011519027.1:c.2700T>C	XP_011517329.1:p.Ser900=
XM_011519029.1:c.1122T>C	XP_011517331.1:p.Ser374=
XM_011519030.1:c.474T>C	XP_011517332.1:p.Ser158=
XM_011519031.1:c.261T>C	XP_011517333.1:p.Ser87=
XM_011519032.1:c.261T>C	XP_011517334.1:p.Ser87=
XM_011519033.1:c.2535T>C	XP_011517335.1:p.Ser845=
NM_001354263.1:c.2670T>C	NP_001341192.1:p.Ser890=
XM_005266105.5:c.2682T>C	XP_005266162.1:p.Ser894=
XM_011519021.3:c.2700T>C	XP_011517323.1:p.Ser900=
XM_011519022.3:c.2697T>C	XP_011517324.1:p.Ser899=
XM_011519023.3:c.2679T>C	XP_011517325.1:p.Ser893=
XM_011519029.3:c.1122T>C	XP_011517331.1:p.Ser374=
XM_011519030.3:c.474T>C	XP_011517332.1:p.Ser158=
XM_017015134.1:c.2676T>C	XP_016870623.1:p.Ser892=
XM_017015136.2:c.2592T>C	XP_016870625.1:p.Ser864=
XM_017015137.1:c.2577T>C	XP_016870626.1:p.Ser859=
XM_017015138.1:c.2577T>C	XP_016870627.1:p.Ser859=
XM_024447674.1:c.2520T>C	XP_024303442.1:p.Ser840=
XM_024447675.1:c.2454T>C	XP_024303443.1:p.Ser818=
XM_024447676.1:c.1815T>C	XP_024303444.1:p.Ser605=
XM_024447677.1:c.1815T>C	XP_024303445.1:p.Ser605=
XM_024447678.1:c.2598T>C	XP_024303446.1:p.Ser866=
XM_024447680.1:c.2433T>C	XP_024303448.1:p.Ser811=
NM_024757.5:c.2691T>C MANE Select	NP_079033.4:p.Ser897=
NM_001354263.2:c.2670T>C	NP_001341192.1:p.Ser890=