Canonical Allele Identifier: CA375774038

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140712590G>T (hg19) ; chr9:g.137818138G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137818138G>T , CM000671.2:g.137818138G>T	GRCh38
NC_000009.11:g.140712590G>T , CM000671.1:g.140712590G>T	GRCh37
NC_000009.10:g.139832411G>T	NCBI36
NG_011776.1:g.204147G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3540G>T MANE Select	ENSP00000417980.1:p.Lys1180Asn
ENST00000636526.1:n.26G>T
ENST00000637161.1:c.3447G>T	ENSP00000490328.1:p.Lys1149Asn
ENST00000637261.1:c.4114G>T	ENSP00000490815.1:n.4114G>T
ENST00000637748.1:n.521G>T
ENST00000637891.1:c.1614G>T	ENSP00000490907.1:n.1614G>T
ENST00000460843.5:c.3540G>T	ENSP00000417980.1:p.Lys1180Asn
ENST00000462942.3:c.2397G>T	ENSP00000436107.1:p.Lys799Asn
ENST00000475564.5:n.1264G>T
ENST00000494249.5:n.893G>T
NM_024757.4:c.3540G>T	NP_079033.4:p.Lys1180Asn
XM_005266105.3:c.3531G>T	XP_005266162.1:p.Lys1177Asn
XM_005266110.1:c.3447G>T	XP_005266167.1:p.Lys1149Asn
XM_006717288.2:c.3522G>T	XP_006717351.1:p.Lys1174Asn
XM_011519021.1:c.3549G>T	XP_011517323.1:p.Lys1183Asn
XM_011519022.1:c.3546G>T	XP_011517324.1:p.Lys1182Asn
XM_011519023.1:c.3528G>T	XP_011517325.1:p.Lys1176Asn
XM_011519024.1:c.3471G>T	XP_011517326.1:p.Lys1157Asn
XM_011519025.1:c.3447G>T	XP_011517327.1:p.Lys1149Asn
XM_011519026.1:c.3405G>T	XP_011517328.1:p.Lys1135Asn
XM_011519029.1:c.1971G>T	XP_011517331.1:p.Lys657Asn
XM_011519030.1:c.1323G>T	XP_011517332.1:p.Lys441Asn
XM_011519031.1:c.1110G>T	XP_011517333.1:p.Lys370Asn
XM_011519032.1:c.1110G>T	XP_011517334.1:p.Lys370Asn
XM_011519033.1:c.3384G>T	XP_011517335.1:p.Lys1128Asn
XR_930459.1:n.5297-3576C>A
NM_001354263.1:c.3519G>T	NP_001341192.1:p.Lys1173Asn
XM_005266105.5:c.3531G>T	XP_005266162.1:p.Lys1177Asn
XM_011519021.3:c.3549G>T	XP_011517323.1:p.Lys1183Asn
XM_011519022.3:c.3546G>T	XP_011517324.1:p.Lys1182Asn
XM_011519023.3:c.3528G>T	XP_011517325.1:p.Lys1176Asn
XM_011519029.3:c.1971G>T	XP_011517331.1:p.Lys657Asn
XM_011519030.3:c.1323G>T	XP_011517332.1:p.Lys441Asn
XM_017015134.1:c.3525G>T	XP_016870623.1:p.Lys1175Asn
XM_017015136.2:c.3441G>T	XP_016870625.1:p.Lys1147Asn
XM_017015137.1:c.3426G>T	XP_016870626.1:p.Lys1142Asn
XM_017015138.1:c.3426G>T	XP_016870627.1:p.Lys1142Asn
XM_024447674.1:c.3369G>T	XP_024303442.1:p.Lys1123Asn
XM_024447675.1:c.3303G>T	XP_024303443.1:p.Lys1101Asn
XM_024447676.1:c.2664G>T	XP_024303444.1:p.Lys888Asn
XM_024447677.1:c.2664G>T	XP_024303445.1:p.Lys888Asn
XM_024447680.1:c.3282G>T	XP_024303448.1:p.Lys1094Asn
NM_024757.5:c.3540G>T MANE Select	NP_079033.4:p.Lys1180Asn
NM_001354263.2:c.3519G>T	NP_001341192.1:p.Lys1173Asn