Canonical Allele Identifier: CA1884685670

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813015_137813019delinsTTCTC , CM000671.2:g.137813015_137813019delinsTTCTC	GRCh38
NC_000009.11:g.140707467_140707471delinsTTCTC , CM000671.1:g.140707467_140707471delinsTTCTC	GRCh37
NC_000009.10:g.139827288_139827292delinsTTCTC	NCBI36
NG_011776.1:g.199024_199028delinsTTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2877_2881delinsTTCTC MANE Select	ENSP00000417980.1:p.Leu959=
ENST00000636027.1:c.2763_2767delinsTTCTC	ENSP00000489961.1:p.Leu921=
ENST00000637161.1:c.2784_2788delinsTTCTC	ENSP00000490328.1:p.Leu928=
ENST00000637261.1:c.2917_2921delinsTTCTC	ENSP00000490815.1:n.2917_2921delinsTTCTC
ENST00000637891.1:c.771_775delinsTTCTC	ENSP00000490907.1:p.Leu257=
ENST00000460843.5:c.2877_2881delinsTTCTC	ENSP00000417980.1:p.Leu959=
ENST00000462942.3:c.1734_1738delinsTTCTC	ENSP00000436107.1:p.Leu578=
ENST00000486164.5:c.564_568delinsTTCTC
ENST00000488242.2:n.403_407delinsTTCTC
NM_024757.4:c.2877_2881delinsTTCTC	NP_079033.4:p.Leu959=
XM_005266105.3:c.2868_2872delinsTTCTC	XP_005266162.1:p.Leu956=
XM_005266110.1:c.2784_2788delinsTTCTC	XP_005266167.1:p.Leu928=
XM_006717288.2:c.2859_2863delinsTTCTC	XP_006717351.1:p.Leu953=
XM_011519021.1:c.2886_2890delinsTTCTC	XP_011517323.1:p.Leu962=
XM_011519022.1:c.2883_2887delinsTTCTC	XP_011517324.1:p.Leu961=
XM_011519023.1:c.2865_2869delinsTTCTC	XP_011517325.1:p.Leu955=
XM_011519024.1:c.2808_2812delinsTTCTC	XP_011517326.1:p.Leu936=
XM_011519025.1:c.2784_2788delinsTTCTC	XP_011517327.1:p.Leu928=
XM_011519026.1:c.2742_2746delinsTTCTC	XP_011517328.1:p.Leu914=
XM_011519029.1:c.1308_1312delinsTTCTC	XP_011517331.1:p.Leu436=
XM_011519030.1:c.660_664delinsTTCTC	XP_011517332.1:p.Leu220=
XM_011519031.1:c.447_451delinsTTCTC	XP_011517333.1:p.Leu149=
XM_011519032.1:c.447_451delinsTTCTC	XP_011517334.1:p.Leu149=
XM_011519033.1:c.2721_2725delinsTTCTC	XP_011517335.1:p.Leu907=
NM_001354263.1:c.2856_2860delinsTTCTC	NP_001341192.1:p.Leu952=
XM_005266105.5:c.2868_2872delinsTTCTC	XP_005266162.1:p.Leu956=
XM_011519021.3:c.2886_2890delinsTTCTC	XP_011517323.1:p.Leu962=
XM_011519022.3:c.2883_2887delinsTTCTC	XP_011517324.1:p.Leu961=
XM_011519023.3:c.2865_2869delinsTTCTC	XP_011517325.1:p.Leu955=
XM_011519029.3:c.1308_1312delinsTTCTC	XP_011517331.1:p.Leu436=
XM_011519030.3:c.660_664delinsTTCTC	XP_011517332.1:p.Leu220=
XM_017015134.1:c.2862_2866delinsTTCTC	XP_016870623.1:p.Leu954=
XM_017015136.2:c.2778_2782delinsTTCTC	XP_016870625.1:p.Leu926=
XM_017015137.1:c.2763_2767delinsTTCTC	XP_016870626.1:p.Leu921=
XM_017015138.1:c.2763_2767delinsTTCTC	XP_016870627.1:p.Leu921=
XM_024447674.1:c.2706_2710delinsTTCTC	XP_024303442.1:p.Leu902=
XM_024447675.1:c.2640_2644delinsTTCTC	XP_024303443.1:p.Leu880=
XM_024447676.1:c.2001_2005delinsTTCTC	XP_024303444.1:p.Leu667=
XM_024447677.1:c.2001_2005delinsTTCTC	XP_024303445.1:p.Leu667=
XM_024447680.1:c.2619_2623delinsTTCTC	XP_024303448.1:p.Leu873=
NM_024757.5:c.2877_2881delinsTTCTC MANE Select	NP_079033.4:p.Leu959=
NM_001354263.2:c.2856_2860delinsTTCTC	NP_001341192.1:p.Leu952=