Canonical Allele Identifier: CA375794615

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707974C>A (hg19) ; chr9:g.137813522C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813522C>A , CM000671.2:g.137813522C>A	GRCh38
NC_000009.11:g.140707974C>A , CM000671.1:g.140707974C>A	GRCh37
NC_000009.10:g.139827795C>A	NCBI36
NG_011776.1:g.199531C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3172C>A MANE Select	ENSP00000417980.1:p.His1058Asn
ENST00000637161.1:c.3079C>A	ENSP00000490328.1:p.His1027Asn
ENST00000637261.1:c.3212C>A	ENSP00000490815.1:n.3212C>A
ENST00000637891.1:c.1066C>A	ENSP00000490907.1:p.His356Asn
ENST00000460843.5:c.3172C>A	ENSP00000417980.1:p.His1058Asn
ENST00000462942.3:c.2029C>A	ENSP00000436107.1:p.His677Asn
ENST00000483653.1:n.32C>A
ENST00000488242.2:n.698C>A
NM_024757.4:c.3172C>A	NP_079033.4:p.His1058Asn
XM_005266105.3:c.3163C>A	XP_005266162.1:p.His1055Asn
XM_005266110.1:c.3079C>A	XP_005266167.1:p.His1027Asn
XM_006717288.2:c.3154C>A	XP_006717351.1:p.His1052Asn
XM_011519021.1:c.3181C>A	XP_011517323.1:p.His1061Asn
XM_011519022.1:c.3178C>A	XP_011517324.1:p.His1060Asn
XM_011519023.1:c.3160C>A	XP_011517325.1:p.His1054Asn
XM_011519024.1:c.3103C>A	XP_011517326.1:p.His1035Asn
XM_011519025.1:c.3079C>A	XP_011517327.1:p.His1027Asn
XM_011519026.1:c.3037C>A	XP_011517328.1:p.His1013Asn
XM_011519029.1:c.1603C>A	XP_011517331.1:p.His535Asn
XM_011519030.1:c.955C>A	XP_011517332.1:p.His319Asn
XM_011519031.1:c.742C>A	XP_011517333.1:p.His248Asn
XM_011519032.1:c.742C>A	XP_011517334.1:p.His248Asn
XM_011519033.1:c.3016C>A	XP_011517335.1:p.His1006Asn
NM_001354263.1:c.3151C>A	NP_001341192.1:p.His1051Asn
XM_005266105.5:c.3163C>A	XP_005266162.1:p.His1055Asn
XM_011519021.3:c.3181C>A	XP_011517323.1:p.His1061Asn
XM_011519022.3:c.3178C>A	XP_011517324.1:p.His1060Asn
XM_011519023.3:c.3160C>A	XP_011517325.1:p.His1054Asn
XM_011519029.3:c.1603C>A	XP_011517331.1:p.His535Asn
XM_011519030.3:c.955C>A	XP_011517332.1:p.His319Asn
XM_017015134.1:c.3157C>A	XP_016870623.1:p.His1053Asn
XM_017015136.2:c.3073C>A	XP_016870625.1:p.His1025Asn
XM_017015137.1:c.3058C>A	XP_016870626.1:p.His1020Asn
XM_017015138.1:c.3058C>A	XP_016870627.1:p.His1020Asn
XM_024447674.1:c.3001C>A	XP_024303442.1:p.His1001Asn
XM_024447675.1:c.2935C>A	XP_024303443.1:p.His979Asn
XM_024447676.1:c.2296C>A	XP_024303444.1:p.His766Asn
XM_024447677.1:c.2296C>A	XP_024303445.1:p.His766Asn
XM_024447680.1:c.2914C>A	XP_024303448.1:p.His972Asn
NM_024757.5:c.3172C>A MANE Select	NP_079033.4:p.His1058Asn
NM_001354263.2:c.3151C>A	NP_001341192.1:p.His1051Asn