Canonical Allele Identifier: CA375773992

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140712585A>T (hg19) ; chr9:g.137818133A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137818133A>T , CM000671.2:g.137818133A>T	GRCh38
NC_000009.11:g.140712585A>T , CM000671.1:g.140712585A>T	GRCh37
NC_000009.10:g.139832406A>T	NCBI36
NG_011776.1:g.204142A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3535A>T MANE Select	ENSP00000417980.1:p.Asn1179Tyr
ENST00000636472.1:n.97A>T
ENST00000636526.1:n.21A>T
ENST00000637161.1:c.3442A>T	ENSP00000490328.1:p.Asn1148Tyr
ENST00000637261.1:c.4109A>T	ENSP00000490815.1:n.4109A>T
ENST00000637748.1:n.516A>T
ENST00000637891.1:c.1609A>T	ENSP00000490907.1:n.1609A>T
ENST00000460843.5:c.3535A>T	ENSP00000417980.1:p.Asn1179Tyr
ENST00000462942.3:c.2392A>T	ENSP00000436107.1:p.Asn798Tyr
ENST00000475564.5:n.1259A>T
ENST00000494249.5:n.888A>T
NM_024757.4:c.3535A>T	NP_079033.4:p.Asn1179Tyr
XM_005266105.3:c.3526A>T	XP_005266162.1:p.Asn1176Tyr
XM_005266110.1:c.3442A>T	XP_005266167.1:p.Asn1148Tyr
XM_006717288.2:c.3517A>T	XP_006717351.1:p.Asn1173Tyr
XM_011519021.1:c.3544A>T	XP_011517323.1:p.Asn1182Tyr
XM_011519022.1:c.3541A>T	XP_011517324.1:p.Asn1181Tyr
XM_011519023.1:c.3523A>T	XP_011517325.1:p.Asn1175Tyr
XM_011519024.1:c.3466A>T	XP_011517326.1:p.Asn1156Tyr
XM_011519025.1:c.3442A>T	XP_011517327.1:p.Asn1148Tyr
XM_011519026.1:c.3400A>T	XP_011517328.1:p.Asn1134Tyr
XM_011519029.1:c.1966A>T	XP_011517331.1:p.Asn656Tyr
XM_011519030.1:c.1318A>T	XP_011517332.1:p.Asn440Tyr
XM_011519031.1:c.1105A>T	XP_011517333.1:p.Asn369Tyr
XM_011519032.1:c.1105A>T	XP_011517334.1:p.Asn369Tyr
XM_011519033.1:c.3379A>T	XP_011517335.1:p.Asn1127Tyr
XR_930459.1:n.5297-3571T>A
NM_001354263.1:c.3514A>T	NP_001341192.1:p.Asn1172Tyr
XM_005266105.5:c.3526A>T	XP_005266162.1:p.Asn1176Tyr
XM_011519021.3:c.3544A>T	XP_011517323.1:p.Asn1182Tyr
XM_011519022.3:c.3541A>T	XP_011517324.1:p.Asn1181Tyr
XM_011519023.3:c.3523A>T	XP_011517325.1:p.Asn1175Tyr
XM_011519029.3:c.1966A>T	XP_011517331.1:p.Asn656Tyr
XM_011519030.3:c.1318A>T	XP_011517332.1:p.Asn440Tyr
XM_017015134.1:c.3520A>T	XP_016870623.1:p.Asn1174Tyr
XM_017015136.2:c.3436A>T	XP_016870625.1:p.Asn1146Tyr
XM_017015137.1:c.3421A>T	XP_016870626.1:p.Asn1141Tyr
XM_017015138.1:c.3421A>T	XP_016870627.1:p.Asn1141Tyr
XM_024447674.1:c.3364A>T	XP_024303442.1:p.Asn1122Tyr
XM_024447675.1:c.3298A>T	XP_024303443.1:p.Asn1100Tyr
XM_024447676.1:c.2659A>T	XP_024303444.1:p.Asn887Tyr
XM_024447677.1:c.2659A>T	XP_024303445.1:p.Asn887Tyr
XM_024447680.1:c.3277A>T	XP_024303448.1:p.Asn1093Tyr
NM_024757.5:c.3535A>T MANE Select	NP_079033.4:p.Asn1179Tyr
NM_001354263.2:c.3514A>T	NP_001341192.1:p.Asn1172Tyr