Canonical Allele Identifier: CA467877647

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695398C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800946C>T , CM000671.2:g.137800946C>T	GRCh38
NC_000009.11:g.140695398C>T , CM000671.1:g.140695398C>T	GRCh37
NC_000009.10:g.139815219C>T	NCBI36
NG_011776.1:g.186955C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2674C>T MANE Select	ENSP00000417980.1:p.Leu892=
ENST00000636027.1:c.2560C>T	ENSP00000489961.1:p.Leu854=
ENST00000637161.1:c.2581C>T	ENSP00000490328.1:p.Leu861=
ENST00000637261.1:c.2714C>T	ENSP00000490815.1:n.2714C>T
ENST00000637891.1:c.568C>T	ENSP00000490907.1:p.Leu190=
ENST00000637949.1:c.352C>T	ENSP00000489786.1:p.Leu118=
ENST00000460843.5:c.2674C>T	ENSP00000417980.1:p.Leu892=
ENST00000462942.3:c.1531C>T	ENSP00000436107.1:p.Leu511=
ENST00000482340.5:c.244C>T	ENSP00000486748.1:p.Leu82=
ENST00000486164.5:c.252C>T
ENST00000488242.2:n.200C>T
ENST00000493484.5:c.244C>T	ENSP00000486503.1:p.Leu82=
NM_024757.4:c.2674C>T	NP_079033.4:p.Leu892=
XM_005266105.3:c.2665C>T	XP_005266162.1:p.Leu889=
XM_005266110.1:c.2581C>T	XP_005266167.1:p.Leu861=
XM_006717288.2:c.2656C>T	XP_006717351.1:p.Leu886=
XM_011519021.1:c.2683C>T	XP_011517323.1:p.Leu895=
XM_011519022.1:c.2680C>T	XP_011517324.1:p.Leu894=
XM_011519023.1:c.2662C>T	XP_011517325.1:p.Leu888=
XM_011519024.1:c.2605C>T	XP_011517326.1:p.Leu869=
XM_011519025.1:c.2581C>T	XP_011517327.1:p.Leu861=
XM_011519026.1:c.2539C>T	XP_011517328.1:p.Leu847=
XM_011519027.1:c.2683C>T	XP_011517329.1:p.Leu895=
XM_011519029.1:c.1105C>T	XP_011517331.1:p.Leu369=
XM_011519030.1:c.457C>T	XP_011517332.1:p.Leu153=
XM_011519031.1:c.244C>T	XP_011517333.1:p.Leu82=
XM_011519032.1:c.244C>T	XP_011517334.1:p.Leu82=
XM_011519033.1:c.2518C>T	XP_011517335.1:p.Leu840=
NM_001354263.1:c.2653C>T	NP_001341192.1:p.Leu885=
XM_005266105.5:c.2665C>T	XP_005266162.1:p.Leu889=
XM_011519021.3:c.2683C>T	XP_011517323.1:p.Leu895=
XM_011519022.3:c.2680C>T	XP_011517324.1:p.Leu894=
XM_011519023.3:c.2662C>T	XP_011517325.1:p.Leu888=
XM_011519029.3:c.1105C>T	XP_011517331.1:p.Leu369=
XM_011519030.3:c.457C>T	XP_011517332.1:p.Leu153=
XM_017015134.1:c.2659C>T	XP_016870623.1:p.Leu887=
XM_017015136.2:c.2575C>T	XP_016870625.1:p.Leu859=
XM_017015137.1:c.2560C>T	XP_016870626.1:p.Leu854=
XM_017015138.1:c.2560C>T	XP_016870627.1:p.Leu854=
XM_024447674.1:c.2503C>T	XP_024303442.1:p.Leu835=
XM_024447675.1:c.2437C>T	XP_024303443.1:p.Leu813=
XM_024447676.1:c.1798C>T	XP_024303444.1:p.Leu600=
XM_024447677.1:c.1798C>T	XP_024303445.1:p.Leu600=
XM_024447678.1:c.2581C>T	XP_024303446.1:p.Leu861=
XM_024447680.1:c.2416C>T	XP_024303448.1:p.Leu806=
NM_024757.5:c.2674C>T MANE Select	NP_079033.4:p.Leu892=
NM_001354263.2:c.2653C>T	NP_001341192.1:p.Leu885=