Canonical Allele Identifier: CA375794622

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707976T>G (hg19) ; chr9:g.137813524T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813524T>G , CM000671.2:g.137813524T>G	GRCh38
NC_000009.11:g.140707976T>G , CM000671.1:g.140707976T>G	GRCh37
NC_000009.10:g.139827797T>G	NCBI36
NG_011776.1:g.199533T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3174T>G MANE Select	ENSP00000417980.1:p.His1058Gln
ENST00000637161.1:c.3081T>G	ENSP00000490328.1:p.His1027Gln
ENST00000637261.1:c.3214T>G	ENSP00000490815.1:n.3214T>G
ENST00000637891.1:c.1068T>G	ENSP00000490907.1:p.His356Gln
ENST00000460843.5:c.3174T>G	ENSP00000417980.1:p.His1058Gln
ENST00000462942.3:c.2031T>G	ENSP00000436107.1:p.His677Gln
ENST00000483653.1:n.34T>G
ENST00000488242.2:n.700T>G
NM_024757.4:c.3174T>G	NP_079033.4:p.His1058Gln
XM_005266105.3:c.3165T>G	XP_005266162.1:p.His1055Gln
XM_005266110.1:c.3081T>G	XP_005266167.1:p.His1027Gln
XM_006717288.2:c.3156T>G	XP_006717351.1:p.His1052Gln
XM_011519021.1:c.3183T>G	XP_011517323.1:p.His1061Gln
XM_011519022.1:c.3180T>G	XP_011517324.1:p.His1060Gln
XM_011519023.1:c.3162T>G	XP_011517325.1:p.His1054Gln
XM_011519024.1:c.3105T>G	XP_011517326.1:p.His1035Gln
XM_011519025.1:c.3081T>G	XP_011517327.1:p.His1027Gln
XM_011519026.1:c.3039T>G	XP_011517328.1:p.His1013Gln
XM_011519029.1:c.1605T>G	XP_011517331.1:p.His535Gln
XM_011519030.1:c.957T>G	XP_011517332.1:p.His319Gln
XM_011519031.1:c.744T>G	XP_011517333.1:p.His248Gln
XM_011519032.1:c.744T>G	XP_011517334.1:p.His248Gln
XM_011519033.1:c.3018T>G	XP_011517335.1:p.His1006Gln
NM_001354263.1:c.3153T>G	NP_001341192.1:p.His1051Gln
XM_005266105.5:c.3165T>G	XP_005266162.1:p.His1055Gln
XM_011519021.3:c.3183T>G	XP_011517323.1:p.His1061Gln
XM_011519022.3:c.3180T>G	XP_011517324.1:p.His1060Gln
XM_011519023.3:c.3162T>G	XP_011517325.1:p.His1054Gln
XM_011519029.3:c.1605T>G	XP_011517331.1:p.His535Gln
XM_011519030.3:c.957T>G	XP_011517332.1:p.His319Gln
XM_017015134.1:c.3159T>G	XP_016870623.1:p.His1053Gln
XM_017015136.2:c.3075T>G	XP_016870625.1:p.His1025Gln
XM_017015137.1:c.3060T>G	XP_016870626.1:p.His1020Gln
XM_017015138.1:c.3060T>G	XP_016870627.1:p.His1020Gln
XM_024447674.1:c.3003T>G	XP_024303442.1:p.His1001Gln
XM_024447675.1:c.2937T>G	XP_024303443.1:p.His979Gln
XM_024447676.1:c.2298T>G	XP_024303444.1:p.His766Gln
XM_024447677.1:c.2298T>G	XP_024303445.1:p.His766Gln
XM_024447680.1:c.2916T>G	XP_024303448.1:p.His972Gln
NM_024757.5:c.3174T>G MANE Select	NP_079033.4:p.His1058Gln
NM_001354263.2:c.3153T>G	NP_001341192.1:p.His1051Gln