Canonical Allele Identifier: CA375773277

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140712514A>T (hg19) ; chr9:g.137818062A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137818062A>T , CM000671.2:g.137818062A>T	GRCh38
NC_000009.11:g.140712514A>T , CM000671.1:g.140712514A>T	GRCh37
NC_000009.10:g.139832335A>T	NCBI36
NG_011776.1:g.204071A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3464A>T MANE Select	ENSP00000417980.1:p.Tyr1155Phe
ENST00000636472.1:n.26A>T
ENST00000637161.1:c.3371A>T	ENSP00000490328.1:p.Tyr1124Phe
ENST00000637261.1:c.4038A>T	ENSP00000490815.1:n.4038A>T
ENST00000637748.1:n.445A>T
ENST00000637891.1:c.1538A>T	ENSP00000490907.1:n.1538A>T
ENST00000460843.5:c.3464A>T	ENSP00000417980.1:p.Tyr1155Phe
ENST00000462942.3:c.2321A>T	ENSP00000436107.1:p.Tyr774Phe
ENST00000475564.5:n.1188A>T
ENST00000494249.5:n.817A>T
NM_024757.4:c.3464A>T	NP_079033.4:p.Tyr1155Phe
XM_005266105.3:c.3455A>T	XP_005266162.1:p.Tyr1152Phe
XM_005266110.1:c.3371A>T	XP_005266167.1:p.Tyr1124Phe
XM_006717288.2:c.3446A>T	XP_006717351.1:p.Tyr1149Phe
XM_011519021.1:c.3473A>T	XP_011517323.1:p.Tyr1158Phe
XM_011519022.1:c.3470A>T	XP_011517324.1:p.Tyr1157Phe
XM_011519023.1:c.3452A>T	XP_011517325.1:p.Tyr1151Phe
XM_011519024.1:c.3395A>T	XP_011517326.1:p.Tyr1132Phe
XM_011519025.1:c.3371A>T	XP_011517327.1:p.Tyr1124Phe
XM_011519026.1:c.3329A>T	XP_011517328.1:p.Tyr1110Phe
XM_011519029.1:c.1895A>T	XP_011517331.1:p.Tyr632Phe
XM_011519030.1:c.1247A>T	XP_011517332.1:p.Tyr416Phe
XM_011519031.1:c.1034A>T	XP_011517333.1:p.Tyr345Phe
XM_011519032.1:c.1034A>T	XP_011517334.1:p.Tyr345Phe
XM_011519033.1:c.3308A>T	XP_011517335.1:p.Tyr1103Phe
XR_930459.1:n.5297-3500T>A
NM_001354263.1:c.3443A>T	NP_001341192.1:p.Tyr1148Phe
XM_005266105.5:c.3455A>T	XP_005266162.1:p.Tyr1152Phe
XM_011519021.3:c.3473A>T	XP_011517323.1:p.Tyr1158Phe
XM_011519022.3:c.3470A>T	XP_011517324.1:p.Tyr1157Phe
XM_011519023.3:c.3452A>T	XP_011517325.1:p.Tyr1151Phe
XM_011519029.3:c.1895A>T	XP_011517331.1:p.Tyr632Phe
XM_011519030.3:c.1247A>T	XP_011517332.1:p.Tyr416Phe
XM_017015134.1:c.3449A>T	XP_016870623.1:p.Tyr1150Phe
XM_017015136.2:c.3365A>T	XP_016870625.1:p.Tyr1122Phe
XM_017015137.1:c.3350A>T	XP_016870626.1:p.Tyr1117Phe
XM_017015138.1:c.3350A>T	XP_016870627.1:p.Tyr1117Phe
XM_024447674.1:c.3293A>T	XP_024303442.1:p.Tyr1098Phe
XM_024447675.1:c.3227A>T	XP_024303443.1:p.Tyr1076Phe
XM_024447676.1:c.2588A>T	XP_024303444.1:p.Tyr863Phe
XM_024447677.1:c.2588A>T	XP_024303445.1:p.Tyr863Phe
XM_024447680.1:c.3206A>T	XP_024303448.1:p.Tyr1069Phe
NM_024757.5:c.3464A>T MANE Select	NP_079033.4:p.Tyr1155Phe
NM_001354263.2:c.3443A>T	NP_001341192.1:p.Tyr1148Phe