Canonical Allele Identifier: CA375789011

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695417A>C (hg19) ; chr9:g.137800965A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800965A>C , CM000671.2:g.137800965A>C	GRCh38
NC_000009.11:g.140695417A>C , CM000671.1:g.140695417A>C	GRCh37
NC_000009.10:g.139815238A>C	NCBI36
NG_011776.1:g.186974A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2693A>C MANE Select	ENSP00000417980.1:p.Asp898Ala
ENST00000636027.1:c.2579A>C	ENSP00000489961.1:p.Asp860Ala
ENST00000637161.1:c.2600A>C	ENSP00000490328.1:p.Asp867Ala
ENST00000637261.1:c.2733A>C	ENSP00000490815.1:n.2733A>C
ENST00000637891.1:c.587A>C	ENSP00000490907.1:p.Asp196Ala
ENST00000637949.1:c.371A>C	ENSP00000489786.1:p.Asp124Ala
ENST00000460843.5:c.2693A>C	ENSP00000417980.1:p.Asp898Ala
ENST00000462942.3:c.1550A>C	ENSP00000436107.1:p.Asp517Ala
ENST00000482340.5:c.263A>C	ENSP00000486748.1:p.Asp88Ala
ENST00000486164.5:c.271A>C
ENST00000488242.2:n.219A>C
ENST00000493484.5:c.263A>C	ENSP00000486503.1:p.Asp88Ala
NM_024757.4:c.2693A>C	NP_079033.4:p.Asp898Ala
XM_005266105.3:c.2684A>C	XP_005266162.1:p.Asp895Ala
XM_005266110.1:c.2600A>C	XP_005266167.1:p.Asp867Ala
XM_006717288.2:c.2675A>C	XP_006717351.1:p.Asp892Ala
XM_011519021.1:c.2702A>C	XP_011517323.1:p.Asp901Ala
XM_011519022.1:c.2699A>C	XP_011517324.1:p.Asp900Ala
XM_011519023.1:c.2681A>C	XP_011517325.1:p.Asp894Ala
XM_011519024.1:c.2624A>C	XP_011517326.1:p.Asp875Ala
XM_011519025.1:c.2600A>C	XP_011517327.1:p.Asp867Ala
XM_011519026.1:c.2558A>C	XP_011517328.1:p.Asp853Ala
XM_011519027.1:c.2702A>C	XP_011517329.1:p.Asp901Ala
XM_011519029.1:c.1124A>C	XP_011517331.1:p.Asp375Ala
XM_011519030.1:c.476A>C	XP_011517332.1:p.Asp159Ala
XM_011519031.1:c.263A>C	XP_011517333.1:p.Asp88Ala
XM_011519032.1:c.263A>C	XP_011517334.1:p.Asp88Ala
XM_011519033.1:c.2537A>C	XP_011517335.1:p.Asp846Ala
NM_001354263.1:c.2672A>C	NP_001341192.1:p.Asp891Ala
XM_005266105.5:c.2684A>C	XP_005266162.1:p.Asp895Ala
XM_011519021.3:c.2702A>C	XP_011517323.1:p.Asp901Ala
XM_011519022.3:c.2699A>C	XP_011517324.1:p.Asp900Ala
XM_011519023.3:c.2681A>C	XP_011517325.1:p.Asp894Ala
XM_011519029.3:c.1124A>C	XP_011517331.1:p.Asp375Ala
XM_011519030.3:c.476A>C	XP_011517332.1:p.Asp159Ala
XM_017015134.1:c.2678A>C	XP_016870623.1:p.Asp893Ala
XM_017015136.2:c.2594A>C	XP_016870625.1:p.Asp865Ala
XM_017015137.1:c.2579A>C	XP_016870626.1:p.Asp860Ala
XM_017015138.1:c.2579A>C	XP_016870627.1:p.Asp860Ala
XM_024447674.1:c.2522A>C	XP_024303442.1:p.Asp841Ala
XM_024447675.1:c.2456A>C	XP_024303443.1:p.Asp819Ala
XM_024447676.1:c.1817A>C	XP_024303444.1:p.Asp606Ala
XM_024447677.1:c.1817A>C	XP_024303445.1:p.Asp606Ala
XM_024447678.1:c.2600A>C	XP_024303446.1:p.Asp867Ala
XM_024447680.1:c.2435A>C	XP_024303448.1:p.Asp812Ala
NM_024757.5:c.2693A>C MANE Select	NP_079033.4:p.Asp898Ala
NM_001354263.2:c.2672A>C	NP_001341192.1:p.Asp891Ala