Canonical Allele Identifier: CA468161069

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707545G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813093G>T , CM000671.2:g.137813093G>T	GRCh38
NC_000009.11:g.140707545G>T , CM000671.1:g.140707545G>T	GRCh37
NC_000009.10:g.139827366G>T	NCBI36
NG_011776.1:g.199102G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2955G>T MANE Select	ENSP00000417980.1:p.Val985=
ENST00000636027.1:c.2841G>T	ENSP00000489961.1:p.Val947=
ENST00000637161.1:c.2862G>T	ENSP00000490328.1:p.Val954=
ENST00000637261.1:c.2995G>T	ENSP00000490815.1:n.2995G>T
ENST00000637891.1:c.849G>T	ENSP00000490907.1:p.Val283=
ENST00000460843.5:c.2955G>T	ENSP00000417980.1:p.Val985=
ENST00000462942.3:c.1812G>T	ENSP00000436107.1:p.Val604=
ENST00000486164.5:c.642G>T
ENST00000488242.2:n.481G>T
NM_024757.4:c.2955G>T	NP_079033.4:p.Val985=
XM_005266105.3:c.2946G>T	XP_005266162.1:p.Val982=
XM_005266110.1:c.2862G>T	XP_005266167.1:p.Val954=
XM_006717288.2:c.2937G>T	XP_006717351.1:p.Val979=
XM_011519021.1:c.2964G>T	XP_011517323.1:p.Val988=
XM_011519022.1:c.2961G>T	XP_011517324.1:p.Val987=
XM_011519023.1:c.2943G>T	XP_011517325.1:p.Val981=
XM_011519024.1:c.2886G>T	XP_011517326.1:p.Val962=
XM_011519025.1:c.2862G>T	XP_011517327.1:p.Val954=
XM_011519026.1:c.2820G>T	XP_011517328.1:p.Val940=
XM_011519029.1:c.1386G>T	XP_011517331.1:p.Val462=
XM_011519030.1:c.738G>T	XP_011517332.1:p.Val246=
XM_011519031.1:c.525G>T	XP_011517333.1:p.Val175=
XM_011519032.1:c.525G>T	XP_011517334.1:p.Val175=
XM_011519033.1:c.2799G>T	XP_011517335.1:p.Val933=
NM_001354263.1:c.2934G>T	NP_001341192.1:p.Val978=
XM_005266105.5:c.2946G>T	XP_005266162.1:p.Val982=
XM_011519021.3:c.2964G>T	XP_011517323.1:p.Val988=
XM_011519022.3:c.2961G>T	XP_011517324.1:p.Val987=
XM_011519023.3:c.2943G>T	XP_011517325.1:p.Val981=
XM_011519029.3:c.1386G>T	XP_011517331.1:p.Val462=
XM_011519030.3:c.738G>T	XP_011517332.1:p.Val246=
XM_017015134.1:c.2940G>T	XP_016870623.1:p.Val980=
XM_017015136.2:c.2856G>T	XP_016870625.1:p.Val952=
XM_017015137.1:c.2841G>T	XP_016870626.1:p.Val947=
XM_017015138.1:c.2841G>T	XP_016870627.1:p.Val947=
XM_024447674.1:c.2784G>T	XP_024303442.1:p.Val928=
XM_024447675.1:c.2718G>T	XP_024303443.1:p.Val906=
XM_024447676.1:c.2079G>T	XP_024303444.1:p.Val693=
XM_024447677.1:c.2079G>T	XP_024303445.1:p.Val693=
XM_024447680.1:c.2697G>T	XP_024303448.1:p.Val899=
NM_024757.5:c.2955G>T MANE Select	NP_079033.4:p.Val985=
NM_001354263.2:c.2934G>T	NP_001341192.1:p.Val978=