Canonical Allele Identifier: CA1884679413

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137801195_137801196delinsGA , CM000671.2:g.137801195_137801196delinsGA	GRCh38
NC_000009.11:g.140695647_140695648delinsGA , CM000671.1:g.140695647_140695648delinsGA	GRCh37
NC_000009.10:g.139815468_139815469delinsGA	NCBI36
NG_011776.1:g.187204_187205delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2712+211_2712+212delinsGA MANE Select	ENSP00000417980.1:n.2712+211_2712+212delinsGA
ENST00000636027.1:c.2598+211_2598+212delinsGA	ENSP00000489961.1:n.2598+211_2598+212delinsGA
ENST00000637161.1:c.2619+211_2619+212delinsGA	ENSP00000490328.1:n.2619+211_2619+212delinsGA
ENST00000637261.1:c.2752+211_2752+212delinsGA	ENSP00000490815.1:n.2752+211_2752+212delinsGA
ENST00000637891.1:c.606+211_606+212delinsGA	ENSP00000490907.1:n.606+211_606+212delinsGA
ENST00000637949.1:c.390+211_390+212delinsGA	ENSP00000489786.1:n.390+211_390+212delinsGA
ENST00000460843.5:c.2712+211_2712+212delinsGA	ENSP00000417980.1:n.2712+211_2712+212delinsGA
ENST00000462942.3:c.1569+211_1569+212delinsGA	ENSP00000436107.1:n.1569+211_1569+212delinsGA
ENST00000482340.5:c.282+211_282+212delinsGA	ENSP00000486748.1:n.282+211_282+212delinsGA
ENST00000486164.5:c.290+211_290+212delinsGA
ENST00000488242.2:n.238+211_238+212delinsGA
ENST00000493484.5:c.282+211_282+212delinsGA	ENSP00000486503.1:n.282+211_282+212delinsGA
NM_024757.4:c.2712+211_2712+212delinsGA	NP_079033.4:n.2712+211_2712+212delinsGA
XM_005266105.3:c.2703+211_2703+212delinsGA	XP_005266162.1:n.2703+211_2703+212delinsGA
XM_005266110.1:c.2619+211_2619+212delinsGA	XP_005266167.1:n.2619+211_2619+212delinsGA
XM_006717288.2:c.2694+211_2694+212delinsGA	XP_006717351.1:n.2694+211_2694+212delinsGA
XM_011519021.1:c.2721+211_2721+212delinsGA	XP_011517323.1:n.2721+211_2721+212delinsGA
XM_011519022.1:c.2718+211_2718+212delinsGA	XP_011517324.1:n.2718+211_2718+212delinsGA
XM_011519023.1:c.2700+211_2700+212delinsGA	XP_011517325.1:n.2700+211_2700+212delinsGA
XM_011519024.1:c.2643+211_2643+212delinsGA	XP_011517326.1:n.2643+211_2643+212delinsGA
XM_011519025.1:c.2619+211_2619+212delinsGA	XP_011517327.1:n.2619+211_2619+212delinsGA
XM_011519026.1:c.2577+211_2577+212delinsGA	XP_011517328.1:n.2577+211_2577+212delinsGA
XM_011519027.1:c.2721+211_2721+212delinsGA	XP_011517329.1:n.2721+211_2721+212delinsGA
XM_011519029.1:c.1143+211_1143+212delinsGA	XP_011517331.1:n.1143+211_1143+212delinsGA
XM_011519030.1:c.495+211_495+212delinsGA	XP_011517332.1:n.495+211_495+212delinsGA
XM_011519031.1:c.282+211_282+212delinsGA	XP_011517333.1:n.282+211_282+212delinsGA
XM_011519032.1:c.282+211_282+212delinsGA	XP_011517334.1:n.282+211_282+212delinsGA
XM_011519033.1:c.2556+211_2556+212delinsGA	XP_011517335.1:n.2556+211_2556+212delinsGA
NM_001354263.1:c.2691+211_2691+212delinsGA	NP_001341192.1:n.2691+211_2691+212delinsGA
XM_005266105.5:c.2703+211_2703+212delinsGA	XP_005266162.1:n.2703+211_2703+212delinsGA
XM_011519021.3:c.2721+211_2721+212delinsGA	XP_011517323.1:n.2721+211_2721+212delinsGA
XM_011519022.3:c.2718+211_2718+212delinsGA	XP_011517324.1:n.2718+211_2718+212delinsGA
XM_011519023.3:c.2700+211_2700+212delinsGA	XP_011517325.1:n.2700+211_2700+212delinsGA
XM_011519029.3:c.1143+211_1143+212delinsGA	XP_011517331.1:n.1143+211_1143+212delinsGA
XM_011519030.3:c.495+211_495+212delinsGA	XP_011517332.1:n.495+211_495+212delinsGA
XM_017015134.1:c.2697+211_2697+212delinsGA	XP_016870623.1:n.2697+211_2697+212delinsGA
XM_017015136.2:c.2613+211_2613+212delinsGA	XP_016870625.1:n.2613+211_2613+212delinsGA
XM_017015137.1:c.2598+211_2598+212delinsGA	XP_016870626.1:n.2598+211_2598+212delinsGA
XM_017015138.1:c.2598+211_2598+212delinsGA	XP_016870627.1:n.2598+211_2598+212delinsGA
XM_024447674.1:c.2541+211_2541+212delinsGA	XP_024303442.1:n.2541+211_2541+212delinsGA
XM_024447675.1:c.2475+211_2475+212delinsGA	XP_024303443.1:n.2475+211_2475+212delinsGA
XM_024447676.1:c.1836+211_1836+212delinsGA	XP_024303444.1:n.1836+211_1836+212delinsGA
XM_024447677.1:c.1836+211_1836+212delinsGA	XP_024303445.1:n.1836+211_1836+212delinsGA
XM_024447678.1:c.2619+211_2619+212delinsGA	XP_024303446.1:n.2619+211_2619+212delinsGA
XM_024447680.1:c.2454+211_2454+212delinsGA	XP_024303448.1:n.2454+211_2454+212delinsGA
NM_024757.5:c.2712+211_2712+212delinsGA MANE Select	NP_079033.4:n.2712+211_2712+212delinsGA
NM_001354263.2:c.2691+211_2691+212delinsGA	NP_001341192.1:n.2691+211_2691+212delinsGA