Canonical Allele Identifier: CA1884685712

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813113_137813114delinsGC , CM000671.2:g.137813113_137813114delinsGC	GRCh38
NC_000009.11:g.140707565_140707566delinsGC , CM000671.1:g.140707565_140707566delinsGC	GRCh37
NC_000009.10:g.139827386_139827387delinsGC	NCBI36
NG_011776.1:g.199122_199123delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2975_2976delinsGC MANE Select	ENSP00000417980.1:p.Ser992=
ENST00000636027.1:c.2861_2862delinsGC	ENSP00000489961.1:p.Ser954=
ENST00000637161.1:c.2882_2883delinsGC	ENSP00000490328.1:p.Ser961=
ENST00000637261.1:c.3015_3016delinsGC	ENSP00000490815.1:n.3015_3016delinsGC
ENST00000637891.1:c.869_870delinsGC	ENSP00000490907.1:p.Ser290=
ENST00000460843.5:c.2975_2976delinsGC	ENSP00000417980.1:p.Ser992=
ENST00000462942.3:c.1832_1833delinsGC	ENSP00000436107.1:p.Ser611=
ENST00000486164.5:c.662_663delinsGC
ENST00000488242.2:n.501_502delinsGC
NM_024757.4:c.2975_2976delinsGC	NP_079033.4:p.Ser992=
XM_005266105.3:c.2966_2967delinsGC	XP_005266162.1:p.Ser989=
XM_005266110.1:c.2882_2883delinsGC	XP_005266167.1:p.Ser961=
XM_006717288.2:c.2957_2958delinsGC	XP_006717351.1:p.Ser986=
XM_011519021.1:c.2984_2985delinsGC	XP_011517323.1:p.Ser995=
XM_011519022.1:c.2981_2982delinsGC	XP_011517324.1:p.Ser994=
XM_011519023.1:c.2963_2964delinsGC	XP_011517325.1:p.Ser988=
XM_011519024.1:c.2906_2907delinsGC	XP_011517326.1:p.Ser969=
XM_011519025.1:c.2882_2883delinsGC	XP_011517327.1:p.Ser961=
XM_011519026.1:c.2840_2841delinsGC	XP_011517328.1:p.Ser947=
XM_011519029.1:c.1406_1407delinsGC	XP_011517331.1:p.Ser469=
XM_011519030.1:c.758_759delinsGC	XP_011517332.1:p.Ser253=
XM_011519031.1:c.545_546delinsGC	XP_011517333.1:p.Ser182=
XM_011519032.1:c.545_546delinsGC	XP_011517334.1:p.Ser182=
XM_011519033.1:c.2819_2820delinsGC	XP_011517335.1:p.Ser940=
NM_001354263.1:c.2954_2955delinsGC	NP_001341192.1:p.Ser985=
XM_005266105.5:c.2966_2967delinsGC	XP_005266162.1:p.Ser989=
XM_011519021.3:c.2984_2985delinsGC	XP_011517323.1:p.Ser995=
XM_011519022.3:c.2981_2982delinsGC	XP_011517324.1:p.Ser994=
XM_011519023.3:c.2963_2964delinsGC	XP_011517325.1:p.Ser988=
XM_011519029.3:c.1406_1407delinsGC	XP_011517331.1:p.Ser469=
XM_011519030.3:c.758_759delinsGC	XP_011517332.1:p.Ser253=
XM_017015134.1:c.2960_2961delinsGC	XP_016870623.1:p.Ser987=
XM_017015136.2:c.2876_2877delinsGC	XP_016870625.1:p.Ser959=
XM_017015137.1:c.2861_2862delinsGC	XP_016870626.1:p.Ser954=
XM_017015138.1:c.2861_2862delinsGC	XP_016870627.1:p.Ser954=
XM_024447674.1:c.2804_2805delinsGC	XP_024303442.1:p.Ser935=
XM_024447675.1:c.2738_2739delinsGC	XP_024303443.1:p.Ser913=
XM_024447676.1:c.2099_2100delinsGC	XP_024303444.1:p.Ser700=
XM_024447677.1:c.2099_2100delinsGC	XP_024303445.1:p.Ser700=
XM_024447680.1:c.2717_2718delinsGC	XP_024303448.1:p.Ser906=
NM_024757.5:c.2975_2976delinsGC MANE Select	NP_079033.4:p.Ser992=
NM_001354263.2:c.2954_2955delinsGC	NP_001341192.1:p.Ser985=