Canonical Allele Identifier: CA1884679470

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137801314_137801318delinsCTTTG , CM000671.2:g.137801314_137801318delinsCTTTG	GRCh38
NC_000009.11:g.140695766_140695770delinsCTTTG , CM000671.1:g.140695766_140695770delinsCTTTG	GRCh37
NC_000009.10:g.139815587_139815591delinsCTTTG	NCBI36
NG_011776.1:g.187323_187327delinsCTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2712+330_2712+334delinsCTTTG MANE Select	ENSP00000417980.1:n.2712+330_2712+334delinsCTTTG
ENST00000636027.1:c.2598+330_2598+334delinsCTTTG	ENSP00000489961.1:n.2598+330_2598+334delinsCTTTG
ENST00000637161.1:c.2619+330_2619+334delinsCTTTG	ENSP00000490328.1:n.2619+330_2619+334delinsCTTTG
ENST00000637261.1:c.2752+330_2752+334delinsCTTTG	ENSP00000490815.1:n.2752+330_2752+334delinsCTTTG
ENST00000637891.1:c.606+330_606+334delinsCTTTG	ENSP00000490907.1:n.606+330_606+334delinsCTTTG
ENST00000637949.1:c.390+330_390+334delinsCTTTG	ENSP00000489786.1:n.390+330_390+334delinsCTTTG
ENST00000460843.5:c.2712+330_2712+334delinsCTTTG	ENSP00000417980.1:n.2712+330_2712+334delinsCTTTG
ENST00000462942.3:c.1569+330_1569+334delinsCTTTG	ENSP00000436107.1:n.1569+330_1569+334delinsCTTTG
ENST00000482340.5:c.282+330_282+334delinsCTTTG	ENSP00000486748.1:n.282+330_282+334delinsCTTTG
ENST00000486164.5:c.290+330_290+334delinsCTTTG
ENST00000488242.2:n.238+330_238+334delinsCTTTG
ENST00000493484.5:c.282+330_282+334delinsCTTTG	ENSP00000486503.1:n.282+330_282+334delinsCTTTG
NM_024757.4:c.2712+330_2712+334delinsCTTTG	NP_079033.4:n.2712+330_2712+334delinsCTTTG
XM_005266105.3:c.2703+330_2703+334delinsCTTTG	XP_005266162.1:n.2703+330_2703+334delinsCTTTG
XM_005266110.1:c.2619+330_2619+334delinsCTTTG	XP_005266167.1:n.2619+330_2619+334delinsCTTTG
XM_006717288.2:c.2694+330_2694+334delinsCTTTG	XP_006717351.1:n.2694+330_2694+334delinsCTTTG
XM_011519021.1:c.2721+330_2721+334delinsCTTTG	XP_011517323.1:n.2721+330_2721+334delinsCTTTG
XM_011519022.1:c.2718+330_2718+334delinsCTTTG	XP_011517324.1:n.2718+330_2718+334delinsCTTTG
XM_011519023.1:c.2700+330_2700+334delinsCTTTG	XP_011517325.1:n.2700+330_2700+334delinsCTTTG
XM_011519024.1:c.2643+330_2643+334delinsCTTTG	XP_011517326.1:n.2643+330_2643+334delinsCTTTG
XM_011519025.1:c.2619+330_2619+334delinsCTTTG	XP_011517327.1:n.2619+330_2619+334delinsCTTTG
XM_011519026.1:c.2577+330_2577+334delinsCTTTG	XP_011517328.1:n.2577+330_2577+334delinsCTTTG
XM_011519027.1:c.2721+330_2721+334delinsCTTTG	XP_011517329.1:n.2721+330_2721+334delinsCTTTG
XM_011519029.1:c.1143+330_1143+334delinsCTTTG	XP_011517331.1:n.1143+330_1143+334delinsCTTTG
XM_011519030.1:c.495+330_495+334delinsCTTTG	XP_011517332.1:n.495+330_495+334delinsCTTTG
XM_011519031.1:c.282+330_282+334delinsCTTTG	XP_011517333.1:n.282+330_282+334delinsCTTTG
XM_011519032.1:c.282+330_282+334delinsCTTTG	XP_011517334.1:n.282+330_282+334delinsCTTTG
XM_011519033.1:c.2556+330_2556+334delinsCTTTG	XP_011517335.1:n.2556+330_2556+334delinsCTTTG
NM_001354263.1:c.2691+330_2691+334delinsCTTTG	NP_001341192.1:n.2691+330_2691+334delinsCTTTG
XM_005266105.5:c.2703+330_2703+334delinsCTTTG	XP_005266162.1:n.2703+330_2703+334delinsCTTTG
XM_011519021.3:c.2721+330_2721+334delinsCTTTG	XP_011517323.1:n.2721+330_2721+334delinsCTTTG
XM_011519022.3:c.2718+330_2718+334delinsCTTTG	XP_011517324.1:n.2718+330_2718+334delinsCTTTG
XM_011519023.3:c.2700+330_2700+334delinsCTTTG	XP_011517325.1:n.2700+330_2700+334delinsCTTTG
XM_011519029.3:c.1143+330_1143+334delinsCTTTG	XP_011517331.1:n.1143+330_1143+334delinsCTTTG
XM_011519030.3:c.495+330_495+334delinsCTTTG	XP_011517332.1:n.495+330_495+334delinsCTTTG
XM_017015134.1:c.2697+330_2697+334delinsCTTTG	XP_016870623.1:n.2697+330_2697+334delinsCTTTG
XM_017015136.2:c.2613+330_2613+334delinsCTTTG	XP_016870625.1:n.2613+330_2613+334delinsCTTTG
XM_017015137.1:c.2598+330_2598+334delinsCTTTG	XP_016870626.1:n.2598+330_2598+334delinsCTTTG
XM_017015138.1:c.2598+330_2598+334delinsCTTTG	XP_016870627.1:n.2598+330_2598+334delinsCTTTG
XM_024447674.1:c.2541+330_2541+334delinsCTTTG	XP_024303442.1:n.2541+330_2541+334delinsCTTTG
XM_024447675.1:c.2475+330_2475+334delinsCTTTG	XP_024303443.1:n.2475+330_2475+334delinsCTTTG
XM_024447676.1:c.1836+330_1836+334delinsCTTTG	XP_024303444.1:n.1836+330_1836+334delinsCTTTG
XM_024447677.1:c.1836+330_1836+334delinsCTTTG	XP_024303445.1:n.1836+330_1836+334delinsCTTTG
XM_024447678.1:c.2619+330_2619+334delinsCTTTG	XP_024303446.1:n.2619+330_2619+334delinsCTTTG
XM_024447680.1:c.2454+330_2454+334delinsCTTTG	XP_024303448.1:n.2454+330_2454+334delinsCTTTG
NM_024757.5:c.2712+330_2712+334delinsCTTTG MANE Select	NP_079033.4:n.2712+330_2712+334delinsCTTTG
NM_001354263.2:c.2691+330_2691+334delinsCTTTG	NP_001341192.1:n.2691+330_2691+334delinsCTTTG