Canonical Allele Identifier: CA467877668

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695418C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800966C>T , CM000671.2:g.137800966C>T	GRCh38
NC_000009.11:g.140695418C>T , CM000671.1:g.140695418C>T	GRCh37
NC_000009.10:g.139815239C>T	NCBI36
NG_011776.1:g.186975C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2694C>T MANE Select	ENSP00000417980.1:p.Asp898=
ENST00000636027.1:c.2580C>T	ENSP00000489961.1:p.Asp860=
ENST00000637161.1:c.2601C>T	ENSP00000490328.1:p.Asp867=
ENST00000637261.1:c.2734C>T	ENSP00000490815.1:n.2734C>T
ENST00000637891.1:c.588C>T	ENSP00000490907.1:p.Asp196=
ENST00000637949.1:c.372C>T	ENSP00000489786.1:p.Asp124=
ENST00000460843.5:c.2694C>T	ENSP00000417980.1:p.Asp898=
ENST00000462942.3:c.1551C>T	ENSP00000436107.1:p.Asp517=
ENST00000482340.5:c.264C>T	ENSP00000486748.1:p.Asp88=
ENST00000486164.5:c.272C>T
ENST00000488242.2:n.220C>T
ENST00000493484.5:c.264C>T	ENSP00000486503.1:p.Asp88=
NM_024757.4:c.2694C>T	NP_079033.4:p.Asp898=
XM_005266105.3:c.2685C>T	XP_005266162.1:p.Asp895=
XM_005266110.1:c.2601C>T	XP_005266167.1:p.Asp867=
XM_006717288.2:c.2676C>T	XP_006717351.1:p.Asp892=
XM_011519021.1:c.2703C>T	XP_011517323.1:p.Asp901=
XM_011519022.1:c.2700C>T	XP_011517324.1:p.Asp900=
XM_011519023.1:c.2682C>T	XP_011517325.1:p.Asp894=
XM_011519024.1:c.2625C>T	XP_011517326.1:p.Asp875=
XM_011519025.1:c.2601C>T	XP_011517327.1:p.Asp867=
XM_011519026.1:c.2559C>T	XP_011517328.1:p.Asp853=
XM_011519027.1:c.2703C>T	XP_011517329.1:p.Asp901=
XM_011519029.1:c.1125C>T	XP_011517331.1:p.Asp375=
XM_011519030.1:c.477C>T	XP_011517332.1:p.Asp159=
XM_011519031.1:c.264C>T	XP_011517333.1:p.Asp88=
XM_011519032.1:c.264C>T	XP_011517334.1:p.Asp88=
XM_011519033.1:c.2538C>T	XP_011517335.1:p.Asp846=
NM_001354263.1:c.2673C>T	NP_001341192.1:p.Asp891=
XM_005266105.5:c.2685C>T	XP_005266162.1:p.Asp895=
XM_011519021.3:c.2703C>T	XP_011517323.1:p.Asp901=
XM_011519022.3:c.2700C>T	XP_011517324.1:p.Asp900=
XM_011519023.3:c.2682C>T	XP_011517325.1:p.Asp894=
XM_011519029.3:c.1125C>T	XP_011517331.1:p.Asp375=
XM_011519030.3:c.477C>T	XP_011517332.1:p.Asp159=
XM_017015134.1:c.2679C>T	XP_016870623.1:p.Asp893=
XM_017015136.2:c.2595C>T	XP_016870625.1:p.Asp865=
XM_017015137.1:c.2580C>T	XP_016870626.1:p.Asp860=
XM_017015138.1:c.2580C>T	XP_016870627.1:p.Asp860=
XM_024447674.1:c.2523C>T	XP_024303442.1:p.Asp841=
XM_024447675.1:c.2457C>T	XP_024303443.1:p.Asp819=
XM_024447676.1:c.1818C>T	XP_024303444.1:p.Asp606=
XM_024447677.1:c.1818C>T	XP_024303445.1:p.Asp606=
XM_024447678.1:c.2601C>T	XP_024303446.1:p.Asp867=
XM_024447680.1:c.2436C>T	XP_024303448.1:p.Asp812=
NM_024757.5:c.2694C>T MANE Select	NP_079033.4:p.Asp898=
NM_001354263.2:c.2673C>T	NP_001341192.1:p.Asp891=