Canonical Allele Identifier: CA1884685668

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813007_137813011delinsCTCTT , CM000671.2:g.137813007_137813011delinsCTCTT	GRCh38
NC_000009.11:g.140707459_140707463delinsCTCTT , CM000671.1:g.140707459_140707463delinsCTCTT	GRCh37
NC_000009.10:g.139827280_139827284delinsCTCTT	NCBI36
NG_011776.1:g.199016_199020delinsCTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2869_2873delinsCTCTT MANE Select	ENSP00000417980.1:p.Leu957=
ENST00000636027.1:c.2755_2759delinsCTCTT	ENSP00000489961.1:p.Leu919=
ENST00000637161.1:c.2776_2780delinsCTCTT	ENSP00000490328.1:p.Leu926=
ENST00000637261.1:c.2909_2913delinsCTCTT	ENSP00000490815.1:n.2909_2913delinsCTCTT
ENST00000637891.1:c.763_767delinsCTCTT	ENSP00000490907.1:p.Leu255=
ENST00000460843.5:c.2869_2873delinsCTCTT	ENSP00000417980.1:p.Leu957=
ENST00000462942.3:c.1726_1730delinsCTCTT	ENSP00000436107.1:p.Leu576=
ENST00000486164.5:c.556_560delinsCTCTT
ENST00000488242.2:n.395_399delinsCTCTT
NM_024757.4:c.2869_2873delinsCTCTT	NP_079033.4:p.Leu957=
XM_005266105.3:c.2860_2864delinsCTCTT	XP_005266162.1:p.Leu954=
XM_005266110.1:c.2776_2780delinsCTCTT	XP_005266167.1:p.Leu926=
XM_006717288.2:c.2851_2855delinsCTCTT	XP_006717351.1:p.Leu951=
XM_011519021.1:c.2878_2882delinsCTCTT	XP_011517323.1:p.Leu960=
XM_011519022.1:c.2875_2879delinsCTCTT	XP_011517324.1:p.Leu959=
XM_011519023.1:c.2857_2861delinsCTCTT	XP_011517325.1:p.Leu953=
XM_011519024.1:c.2800_2804delinsCTCTT	XP_011517326.1:p.Leu934=
XM_011519025.1:c.2776_2780delinsCTCTT	XP_011517327.1:p.Leu926=
XM_011519026.1:c.2734_2738delinsCTCTT	XP_011517328.1:p.Leu912=
XM_011519029.1:c.1300_1304delinsCTCTT	XP_011517331.1:p.Leu434=
XM_011519030.1:c.652_656delinsCTCTT	XP_011517332.1:p.Leu218=
XM_011519031.1:c.439_443delinsCTCTT	XP_011517333.1:p.Leu147=
XM_011519032.1:c.439_443delinsCTCTT	XP_011517334.1:p.Leu147=
XM_011519033.1:c.2713_2717delinsCTCTT	XP_011517335.1:p.Leu905=
NM_001354263.1:c.2848_2852delinsCTCTT	NP_001341192.1:p.Leu950=
XM_005266105.5:c.2860_2864delinsCTCTT	XP_005266162.1:p.Leu954=
XM_011519021.3:c.2878_2882delinsCTCTT	XP_011517323.1:p.Leu960=
XM_011519022.3:c.2875_2879delinsCTCTT	XP_011517324.1:p.Leu959=
XM_011519023.3:c.2857_2861delinsCTCTT	XP_011517325.1:p.Leu953=
XM_011519029.3:c.1300_1304delinsCTCTT	XP_011517331.1:p.Leu434=
XM_011519030.3:c.652_656delinsCTCTT	XP_011517332.1:p.Leu218=
XM_017015134.1:c.2854_2858delinsCTCTT	XP_016870623.1:p.Leu952=
XM_017015136.2:c.2770_2774delinsCTCTT	XP_016870625.1:p.Leu924=
XM_017015137.1:c.2755_2759delinsCTCTT	XP_016870626.1:p.Leu919=
XM_017015138.1:c.2755_2759delinsCTCTT	XP_016870627.1:p.Leu919=
XM_024447674.1:c.2698_2702delinsCTCTT	XP_024303442.1:p.Leu900=
XM_024447675.1:c.2632_2636delinsCTCTT	XP_024303443.1:p.Leu878=
XM_024447676.1:c.1993_1997delinsCTCTT	XP_024303444.1:p.Leu665=
XM_024447677.1:c.1993_1997delinsCTCTT	XP_024303445.1:p.Leu665=
XM_024447680.1:c.2611_2615delinsCTCTT	XP_024303448.1:p.Leu871=
NM_024757.5:c.2869_2873delinsCTCTT MANE Select	NP_079033.4:p.Leu957=
NM_001354263.2:c.2848_2852delinsCTCTT	NP_001341192.1:p.Leu950=