Canonical Allele Identifier: CA375793484

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707542G>T (hg19) ; chr9:g.137813090G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813090G>T , CM000671.2:g.137813090G>T	GRCh38
NC_000009.11:g.140707542G>T , CM000671.1:g.140707542G>T	GRCh37
NC_000009.10:g.139827363G>T	NCBI36
NG_011776.1:g.199099G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2952G>T MANE Select	ENSP00000417980.1:p.Gln984His
ENST00000636027.1:c.2838G>T	ENSP00000489961.1:p.Gln946His
ENST00000637161.1:c.2859G>T	ENSP00000490328.1:p.Gln953His
ENST00000637261.1:c.2992G>T	ENSP00000490815.1:n.2992G>T
ENST00000637891.1:c.846G>T	ENSP00000490907.1:p.Gln282His
ENST00000460843.5:c.2952G>T	ENSP00000417980.1:p.Gln984His
ENST00000462942.3:c.1809G>T	ENSP00000436107.1:p.Gln603His
ENST00000486164.5:c.639G>T
ENST00000488242.2:n.478G>T
NM_024757.4:c.2952G>T	NP_079033.4:p.Gln984His
XM_005266105.3:c.2943G>T	XP_005266162.1:p.Gln981His
XM_005266110.1:c.2859G>T	XP_005266167.1:p.Gln953His
XM_006717288.2:c.2934G>T	XP_006717351.1:p.Gln978His
XM_011519021.1:c.2961G>T	XP_011517323.1:p.Gln987His
XM_011519022.1:c.2958G>T	XP_011517324.1:p.Gln986His
XM_011519023.1:c.2940G>T	XP_011517325.1:p.Gln980His
XM_011519024.1:c.2883G>T	XP_011517326.1:p.Gln961His
XM_011519025.1:c.2859G>T	XP_011517327.1:p.Gln953His
XM_011519026.1:c.2817G>T	XP_011517328.1:p.Gln939His
XM_011519029.1:c.1383G>T	XP_011517331.1:p.Gln461His
XM_011519030.1:c.735G>T	XP_011517332.1:p.Gln245His
XM_011519031.1:c.522G>T	XP_011517333.1:p.Gln174His
XM_011519032.1:c.522G>T	XP_011517334.1:p.Gln174His
XM_011519033.1:c.2796G>T	XP_011517335.1:p.Gln932His
NM_001354263.1:c.2931G>T	NP_001341192.1:p.Gln977His
XM_005266105.5:c.2943G>T	XP_005266162.1:p.Gln981His
XM_011519021.3:c.2961G>T	XP_011517323.1:p.Gln987His
XM_011519022.3:c.2958G>T	XP_011517324.1:p.Gln986His
XM_011519023.3:c.2940G>T	XP_011517325.1:p.Gln980His
XM_011519029.3:c.1383G>T	XP_011517331.1:p.Gln461His
XM_011519030.3:c.735G>T	XP_011517332.1:p.Gln245His
XM_017015134.1:c.2937G>T	XP_016870623.1:p.Gln979His
XM_017015136.2:c.2853G>T	XP_016870625.1:p.Gln951His
XM_017015137.1:c.2838G>T	XP_016870626.1:p.Gln946His
XM_017015138.1:c.2838G>T	XP_016870627.1:p.Gln946His
XM_024447674.1:c.2781G>T	XP_024303442.1:p.Gln927His
XM_024447675.1:c.2715G>T	XP_024303443.1:p.Gln905His
XM_024447676.1:c.2076G>T	XP_024303444.1:p.Gln692His
XM_024447677.1:c.2076G>T	XP_024303445.1:p.Gln692His
XM_024447680.1:c.2694G>T	XP_024303448.1:p.Gln898His
NM_024757.5:c.2952G>T MANE Select	NP_079033.4:p.Gln984His
NM_001354263.2:c.2931G>T	NP_001341192.1:p.Gln977His