Canonical Allele Identifier: CA375793564

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707560G>C (hg19) ; chr9:g.137813108G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813108G>C , CM000671.2:g.137813108G>C	GRCh38
NC_000009.11:g.140707560G>C , CM000671.1:g.140707560G>C	GRCh37
NC_000009.10:g.139827381G>C	NCBI36
NG_011776.1:g.199117G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2970G>C MANE Select	ENSP00000417980.1:p.Gln990His
ENST00000636027.1:c.2856G>C	ENSP00000489961.1:p.Gln952His
ENST00000637161.1:c.2877G>C	ENSP00000490328.1:p.Gln959His
ENST00000637261.1:c.3010G>C	ENSP00000490815.1:n.3010G>C
ENST00000637891.1:c.864G>C	ENSP00000490907.1:p.Gln288His
ENST00000460843.5:c.2970G>C	ENSP00000417980.1:p.Gln990His
ENST00000462942.3:c.1827G>C	ENSP00000436107.1:p.Gln609His
ENST00000486164.5:c.657G>C
ENST00000488242.2:n.496G>C
NM_024757.4:c.2970G>C	NP_079033.4:p.Gln990His
XM_005266105.3:c.2961G>C	XP_005266162.1:p.Gln987His
XM_005266110.1:c.2877G>C	XP_005266167.1:p.Gln959His
XM_006717288.2:c.2952G>C	XP_006717351.1:p.Gln984His
XM_011519021.1:c.2979G>C	XP_011517323.1:p.Gln993His
XM_011519022.1:c.2976G>C	XP_011517324.1:p.Gln992His
XM_011519023.1:c.2958G>C	XP_011517325.1:p.Gln986His
XM_011519024.1:c.2901G>C	XP_011517326.1:p.Gln967His
XM_011519025.1:c.2877G>C	XP_011517327.1:p.Gln959His
XM_011519026.1:c.2835G>C	XP_011517328.1:p.Gln945His
XM_011519029.1:c.1401G>C	XP_011517331.1:p.Gln467His
XM_011519030.1:c.753G>C	XP_011517332.1:p.Gln251His
XM_011519031.1:c.540G>C	XP_011517333.1:p.Gln180His
XM_011519032.1:c.540G>C	XP_011517334.1:p.Gln180His
XM_011519033.1:c.2814G>C	XP_011517335.1:p.Gln938His
NM_001354263.1:c.2949G>C	NP_001341192.1:p.Gln983His
XM_005266105.5:c.2961G>C	XP_005266162.1:p.Gln987His
XM_011519021.3:c.2979G>C	XP_011517323.1:p.Gln993His
XM_011519022.3:c.2976G>C	XP_011517324.1:p.Gln992His
XM_011519023.3:c.2958G>C	XP_011517325.1:p.Gln986His
XM_011519029.3:c.1401G>C	XP_011517331.1:p.Gln467His
XM_011519030.3:c.753G>C	XP_011517332.1:p.Gln251His
XM_017015134.1:c.2955G>C	XP_016870623.1:p.Gln985His
XM_017015136.2:c.2871G>C	XP_016870625.1:p.Gln957His
XM_017015137.1:c.2856G>C	XP_016870626.1:p.Gln952His
XM_017015138.1:c.2856G>C	XP_016870627.1:p.Gln952His
XM_024447674.1:c.2799G>C	XP_024303442.1:p.Gln933His
XM_024447675.1:c.2733G>C	XP_024303443.1:p.Gln911His
XM_024447676.1:c.2094G>C	XP_024303444.1:p.Gln698His
XM_024447677.1:c.2094G>C	XP_024303445.1:p.Gln698His
XM_024447680.1:c.2712G>C	XP_024303448.1:p.Gln904His
NM_024757.5:c.2970G>C MANE Select	NP_079033.4:p.Gln990His
NM_001354263.2:c.2949G>C	NP_001341192.1:p.Gln983His