Canonical Allele Identifier: CA375793357

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707505G>T (hg19) ; chr9:g.137813053G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813053G>T , CM000671.2:g.137813053G>T	GRCh38
NC_000009.11:g.140707505G>T , CM000671.1:g.140707505G>T	GRCh37
NC_000009.10:g.139827326G>T	NCBI36
NG_011776.1:g.199062G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2915G>T MANE Select	ENSP00000417980.1:p.Gly972Val
ENST00000636027.1:c.2801G>T	ENSP00000489961.1:p.Gly934Val
ENST00000637161.1:c.2822G>T	ENSP00000490328.1:p.Gly941Val
ENST00000637261.1:c.2955G>T	ENSP00000490815.1:n.2955G>T
ENST00000637891.1:c.809G>T	ENSP00000490907.1:p.Gly270Val
ENST00000460843.5:c.2915G>T	ENSP00000417980.1:p.Gly972Val
ENST00000462942.3:c.1772G>T	ENSP00000436107.1:p.Gly591Val
ENST00000486164.5:c.602G>T
ENST00000488242.2:n.441G>T
NM_024757.4:c.2915G>T	NP_079033.4:p.Gly972Val
XM_005266105.3:c.2906G>T	XP_005266162.1:p.Gly969Val
XM_005266110.1:c.2822G>T	XP_005266167.1:p.Gly941Val
XM_006717288.2:c.2897G>T	XP_006717351.1:p.Gly966Val
XM_011519021.1:c.2924G>T	XP_011517323.1:p.Gly975Val
XM_011519022.1:c.2921G>T	XP_011517324.1:p.Gly974Val
XM_011519023.1:c.2903G>T	XP_011517325.1:p.Gly968Val
XM_011519024.1:c.2846G>T	XP_011517326.1:p.Gly949Val
XM_011519025.1:c.2822G>T	XP_011517327.1:p.Gly941Val
XM_011519026.1:c.2780G>T	XP_011517328.1:p.Gly927Val
XM_011519029.1:c.1346G>T	XP_011517331.1:p.Gly449Val
XM_011519030.1:c.698G>T	XP_011517332.1:p.Gly233Val
XM_011519031.1:c.485G>T	XP_011517333.1:p.Gly162Val
XM_011519032.1:c.485G>T	XP_011517334.1:p.Gly162Val
XM_011519033.1:c.2759G>T	XP_011517335.1:p.Gly920Val
NM_001354263.1:c.2894G>T	NP_001341192.1:p.Gly965Val
XM_005266105.5:c.2906G>T	XP_005266162.1:p.Gly969Val
XM_011519021.3:c.2924G>T	XP_011517323.1:p.Gly975Val
XM_011519022.3:c.2921G>T	XP_011517324.1:p.Gly974Val
XM_011519023.3:c.2903G>T	XP_011517325.1:p.Gly968Val
XM_011519029.3:c.1346G>T	XP_011517331.1:p.Gly449Val
XM_011519030.3:c.698G>T	XP_011517332.1:p.Gly233Val
XM_017015134.1:c.2900G>T	XP_016870623.1:p.Gly967Val
XM_017015136.2:c.2816G>T	XP_016870625.1:p.Gly939Val
XM_017015137.1:c.2801G>T	XP_016870626.1:p.Gly934Val
XM_017015138.1:c.2801G>T	XP_016870627.1:p.Gly934Val
XM_024447674.1:c.2744G>T	XP_024303442.1:p.Gly915Val
XM_024447675.1:c.2678G>T	XP_024303443.1:p.Gly893Val
XM_024447676.1:c.2039G>T	XP_024303444.1:p.Gly680Val
XM_024447677.1:c.2039G>T	XP_024303445.1:p.Gly680Val
XM_024447680.1:c.2657G>T	XP_024303448.1:p.Gly886Val
NM_024757.5:c.2915G>T MANE Select	NP_079033.4:p.Gly972Val
NM_001354263.2:c.2894G>T	NP_001341192.1:p.Gly965Val