Canonical Allele Identifier: CA375788961

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695402T>C (hg19) ; chr9:g.137800950T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800950T>C , CM000671.2:g.137800950T>C	GRCh38
NC_000009.11:g.140695402T>C , CM000671.1:g.140695402T>C	GRCh37
NC_000009.10:g.139815223T>C	NCBI36
NG_011776.1:g.186959T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2678T>C MANE Select	ENSP00000417980.1:p.Leu893Pro
ENST00000636027.1:c.2564T>C	ENSP00000489961.1:p.Leu855Pro
ENST00000637161.1:c.2585T>C	ENSP00000490328.1:p.Leu862Pro
ENST00000637261.1:c.2718T>C	ENSP00000490815.1:n.2718T>C
ENST00000637891.1:c.572T>C	ENSP00000490907.1:p.Leu191Pro
ENST00000637949.1:c.356T>C	ENSP00000489786.1:p.Leu119Pro
ENST00000460843.5:c.2678T>C	ENSP00000417980.1:p.Leu893Pro
ENST00000462942.3:c.1535T>C	ENSP00000436107.1:p.Leu512Pro
ENST00000482340.5:c.248T>C	ENSP00000486748.1:p.Leu83Pro
ENST00000486164.5:c.256T>C
ENST00000488242.2:n.204T>C
ENST00000493484.5:c.248T>C	ENSP00000486503.1:p.Leu83Pro
NM_024757.4:c.2678T>C	NP_079033.4:p.Leu893Pro
XM_005266105.3:c.2669T>C	XP_005266162.1:p.Leu890Pro
XM_005266110.1:c.2585T>C	XP_005266167.1:p.Leu862Pro
XM_006717288.2:c.2660T>C	XP_006717351.1:p.Leu887Pro
XM_011519021.1:c.2687T>C	XP_011517323.1:p.Leu896Pro
XM_011519022.1:c.2684T>C	XP_011517324.1:p.Leu895Pro
XM_011519023.1:c.2666T>C	XP_011517325.1:p.Leu889Pro
XM_011519024.1:c.2609T>C	XP_011517326.1:p.Leu870Pro
XM_011519025.1:c.2585T>C	XP_011517327.1:p.Leu862Pro
XM_011519026.1:c.2543T>C	XP_011517328.1:p.Leu848Pro
XM_011519027.1:c.2687T>C	XP_011517329.1:p.Leu896Pro
XM_011519029.1:c.1109T>C	XP_011517331.1:p.Leu370Pro
XM_011519030.1:c.461T>C	XP_011517332.1:p.Leu154Pro
XM_011519031.1:c.248T>C	XP_011517333.1:p.Leu83Pro
XM_011519032.1:c.248T>C	XP_011517334.1:p.Leu83Pro
XM_011519033.1:c.2522T>C	XP_011517335.1:p.Leu841Pro
NM_001354263.1:c.2657T>C	NP_001341192.1:p.Leu886Pro
XM_005266105.5:c.2669T>C	XP_005266162.1:p.Leu890Pro
XM_011519021.3:c.2687T>C	XP_011517323.1:p.Leu896Pro
XM_011519022.3:c.2684T>C	XP_011517324.1:p.Leu895Pro
XM_011519023.3:c.2666T>C	XP_011517325.1:p.Leu889Pro
XM_011519029.3:c.1109T>C	XP_011517331.1:p.Leu370Pro
XM_011519030.3:c.461T>C	XP_011517332.1:p.Leu154Pro
XM_017015134.1:c.2663T>C	XP_016870623.1:p.Leu888Pro
XM_017015136.2:c.2579T>C	XP_016870625.1:p.Leu860Pro
XM_017015137.1:c.2564T>C	XP_016870626.1:p.Leu855Pro
XM_017015138.1:c.2564T>C	XP_016870627.1:p.Leu855Pro
XM_024447674.1:c.2507T>C	XP_024303442.1:p.Leu836Pro
XM_024447675.1:c.2441T>C	XP_024303443.1:p.Leu814Pro
XM_024447676.1:c.1802T>C	XP_024303444.1:p.Leu601Pro
XM_024447677.1:c.1802T>C	XP_024303445.1:p.Leu601Pro
XM_024447678.1:c.2585T>C	XP_024303446.1:p.Leu862Pro
XM_024447680.1:c.2420T>C	XP_024303448.1:p.Leu807Pro
NM_024757.5:c.2678T>C MANE Select	NP_079033.4:p.Leu893Pro
NM_001354263.2:c.2657T>C	NP_001341192.1:p.Leu886Pro