Canonical Allele Identifier: CA1884685657

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137812972_137812973delinsTA , CM000671.2:g.137812972_137812973delinsTA	GRCh38
NC_000009.11:g.140707424_140707425delinsTA , CM000671.1:g.140707424_140707425delinsTA	GRCh37
NC_000009.10:g.139827245_139827246delinsTA	NCBI36
NG_011776.1:g.198981_198982delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2868-34_2868-33delinsTA MANE Select	ENSP00000417980.1:n.2868-34_2868-33delinsTA
ENST00000636027.1:c.2754-34_2754-33delinsTA	ENSP00000489961.1:n.2754-34_2754-33delinsTA
ENST00000637161.1:c.2775-34_2775-33delinsTA	ENSP00000490328.1:n.2775-34_2775-33delinsTA
ENST00000637261.1:c.2908-34_2908-33delinsTA	ENSP00000490815.1:n.2908-34_2908-33delinsTA
ENST00000637891.1:c.762-34_762-33delinsTA	ENSP00000490907.1:n.762-34_762-33delinsTA
ENST00000460843.5:c.2868-34_2868-33delinsTA	ENSP00000417980.1:n.2868-34_2868-33delinsTA
ENST00000462942.3:c.1725-34_1725-33delinsTA	ENSP00000436107.1:n.1725-34_1725-33delinsTA
ENST00000486164.5:c.555-34_555-33delinsTA
ENST00000488242.2:n.394-34_394-33delinsTA
NM_024757.4:c.2868-34_2868-33delinsTA	NP_079033.4:n.2868-34_2868-33delinsTA
XM_005266105.3:c.2859-34_2859-33delinsTA	XP_005266162.1:n.2859-34_2859-33delinsTA
XM_005266110.1:c.2775-34_2775-33delinsTA	XP_005266167.1:n.2775-34_2775-33delinsTA
XM_006717288.2:c.2850-34_2850-33delinsTA	XP_006717351.1:n.2850-34_2850-33delinsTA
XM_011519021.1:c.2877-34_2877-33delinsTA	XP_011517323.1:n.2877-34_2877-33delinsTA
XM_011519022.1:c.2874-34_2874-33delinsTA	XP_011517324.1:n.2874-34_2874-33delinsTA
XM_011519023.1:c.2856-34_2856-33delinsTA	XP_011517325.1:n.2856-34_2856-33delinsTA
XM_011519024.1:c.2799-34_2799-33delinsTA	XP_011517326.1:n.2799-34_2799-33delinsTA
XM_011519025.1:c.2775-34_2775-33delinsTA	XP_011517327.1:n.2775-34_2775-33delinsTA
XM_011519026.1:c.2733-34_2733-33delinsTA	XP_011517328.1:n.2733-34_2733-33delinsTA
XM_011519029.1:c.1299-34_1299-33delinsTA	XP_011517331.1:n.1299-34_1299-33delinsTA
XM_011519030.1:c.651-34_651-33delinsTA	XP_011517332.1:n.651-34_651-33delinsTA
XM_011519031.1:c.438-34_438-33delinsTA	XP_011517333.1:n.438-34_438-33delinsTA
XM_011519032.1:c.438-34_438-33delinsTA	XP_011517334.1:n.438-34_438-33delinsTA
XM_011519033.1:c.2712-34_2712-33delinsTA	XP_011517335.1:n.2712-34_2712-33delinsTA
NM_001354263.1:c.2847-34_2847-33delinsTA	NP_001341192.1:n.2847-34_2847-33delinsTA
XM_005266105.5:c.2859-34_2859-33delinsTA	XP_005266162.1:n.2859-34_2859-33delinsTA
XM_011519021.3:c.2877-34_2877-33delinsTA	XP_011517323.1:n.2877-34_2877-33delinsTA
XM_011519022.3:c.2874-34_2874-33delinsTA	XP_011517324.1:n.2874-34_2874-33delinsTA
XM_011519023.3:c.2856-34_2856-33delinsTA	XP_011517325.1:n.2856-34_2856-33delinsTA
XM_011519029.3:c.1299-34_1299-33delinsTA	XP_011517331.1:n.1299-34_1299-33delinsTA
XM_011519030.3:c.651-34_651-33delinsTA	XP_011517332.1:n.651-34_651-33delinsTA
XM_017015134.1:c.2853-34_2853-33delinsTA	XP_016870623.1:n.2853-34_2853-33delinsTA
XM_017015136.2:c.2769-34_2769-33delinsTA	XP_016870625.1:n.2769-34_2769-33delinsTA
XM_017015137.1:c.2754-34_2754-33delinsTA	XP_016870626.1:n.2754-34_2754-33delinsTA
XM_017015138.1:c.2754-34_2754-33delinsTA	XP_016870627.1:n.2754-34_2754-33delinsTA
XM_024447674.1:c.2697-34_2697-33delinsTA	XP_024303442.1:n.2697-34_2697-33delinsTA
XM_024447675.1:c.2631-34_2631-33delinsTA	XP_024303443.1:n.2631-34_2631-33delinsTA
XM_024447676.1:c.1992-34_1992-33delinsTA	XP_024303444.1:n.1992-34_1992-33delinsTA
XM_024447677.1:c.1992-34_1992-33delinsTA	XP_024303445.1:n.1992-34_1992-33delinsTA
XM_024447680.1:c.2610-34_2610-33delinsTA	XP_024303448.1:n.2610-34_2610-33delinsTA
NM_024757.5:c.2868-34_2868-33delinsTA MANE Select	NP_079033.4:n.2868-34_2868-33delinsTA
NM_001354263.2:c.2847-34_2847-33delinsTA	NP_001341192.1:n.2847-34_2847-33delinsTA