Canonical Allele Identifier: CA375774029

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140712589A>T (hg19) ; chr9:g.137818137A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137818137A>T , CM000671.2:g.137818137A>T	GRCh38
NC_000009.11:g.140712589A>T , CM000671.1:g.140712589A>T	GRCh37
NC_000009.10:g.139832410A>T	NCBI36
NG_011776.1:g.204146A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3539A>T MANE Select	ENSP00000417980.1:p.Lys1180Met
ENST00000636526.1:n.25A>T
ENST00000637161.1:c.3446A>T	ENSP00000490328.1:p.Lys1149Met
ENST00000637261.1:c.4113A>T	ENSP00000490815.1:n.4113A>T
ENST00000637748.1:n.520A>T
ENST00000637891.1:c.1613A>T	ENSP00000490907.1:n.1613A>T
ENST00000460843.5:c.3539A>T	ENSP00000417980.1:p.Lys1180Met
ENST00000462942.3:c.2396A>T	ENSP00000436107.1:p.Lys799Met
ENST00000475564.5:n.1263A>T
ENST00000494249.5:n.892A>T
NM_024757.4:c.3539A>T	NP_079033.4:p.Lys1180Met
XM_005266105.3:c.3530A>T	XP_005266162.1:p.Lys1177Met
XM_005266110.1:c.3446A>T	XP_005266167.1:p.Lys1149Met
XM_006717288.2:c.3521A>T	XP_006717351.1:p.Lys1174Met
XM_011519021.1:c.3548A>T	XP_011517323.1:p.Lys1183Met
XM_011519022.1:c.3545A>T	XP_011517324.1:p.Lys1182Met
XM_011519023.1:c.3527A>T	XP_011517325.1:p.Lys1176Met
XM_011519024.1:c.3470A>T	XP_011517326.1:p.Lys1157Met
XM_011519025.1:c.3446A>T	XP_011517327.1:p.Lys1149Met
XM_011519026.1:c.3404A>T	XP_011517328.1:p.Lys1135Met
XM_011519029.1:c.1970A>T	XP_011517331.1:p.Lys657Met
XM_011519030.1:c.1322A>T	XP_011517332.1:p.Lys441Met
XM_011519031.1:c.1109A>T	XP_011517333.1:p.Lys370Met
XM_011519032.1:c.1109A>T	XP_011517334.1:p.Lys370Met
XM_011519033.1:c.3383A>T	XP_011517335.1:p.Lys1128Met
XR_930459.1:n.5297-3575T>A
NM_001354263.1:c.3518A>T	NP_001341192.1:p.Lys1173Met
XM_005266105.5:c.3530A>T	XP_005266162.1:p.Lys1177Met
XM_011519021.3:c.3548A>T	XP_011517323.1:p.Lys1183Met
XM_011519022.3:c.3545A>T	XP_011517324.1:p.Lys1182Met
XM_011519023.3:c.3527A>T	XP_011517325.1:p.Lys1176Met
XM_011519029.3:c.1970A>T	XP_011517331.1:p.Lys657Met
XM_011519030.3:c.1322A>T	XP_011517332.1:p.Lys441Met
XM_017015134.1:c.3524A>T	XP_016870623.1:p.Lys1175Met
XM_017015136.2:c.3440A>T	XP_016870625.1:p.Lys1147Met
XM_017015137.1:c.3425A>T	XP_016870626.1:p.Lys1142Met
XM_017015138.1:c.3425A>T	XP_016870627.1:p.Lys1142Met
XM_024447674.1:c.3368A>T	XP_024303442.1:p.Lys1123Met
XM_024447675.1:c.3302A>T	XP_024303443.1:p.Lys1101Met
XM_024447676.1:c.2663A>T	XP_024303444.1:p.Lys888Met
XM_024447677.1:c.2663A>T	XP_024303445.1:p.Lys888Met
XM_024447680.1:c.3281A>T	XP_024303448.1:p.Lys1094Met
NM_024757.5:c.3539A>T MANE Select	NP_079033.4:p.Lys1180Met
NM_001354263.2:c.3518A>T	NP_001341192.1:p.Lys1173Met