Canonical Allele Identifier: CA468161018

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707464T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813012T>C , CM000671.2:g.137813012T>C	GRCh38
NC_000009.11:g.140707464T>C , CM000671.1:g.140707464T>C	GRCh37
NC_000009.10:g.139827285T>C	NCBI36
NG_011776.1:g.199021T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2874T>C MANE Select	ENSP00000417980.1:p.Phe958=
ENST00000636027.1:c.2760T>C	ENSP00000489961.1:p.Phe920=
ENST00000637161.1:c.2781T>C	ENSP00000490328.1:p.Phe927=
ENST00000637261.1:c.2914T>C	ENSP00000490815.1:n.2914T>C
ENST00000637891.1:c.768T>C	ENSP00000490907.1:p.Phe256=
ENST00000460843.5:c.2874T>C	ENSP00000417980.1:p.Phe958=
ENST00000462942.3:c.1731T>C	ENSP00000436107.1:p.Phe577=
ENST00000486164.5:c.561T>C
ENST00000488242.2:n.400T>C
NM_024757.4:c.2874T>C	NP_079033.4:p.Phe958=
XM_005266105.3:c.2865T>C	XP_005266162.1:p.Phe955=
XM_005266110.1:c.2781T>C	XP_005266167.1:p.Phe927=
XM_006717288.2:c.2856T>C	XP_006717351.1:p.Phe952=
XM_011519021.1:c.2883T>C	XP_011517323.1:p.Phe961=
XM_011519022.1:c.2880T>C	XP_011517324.1:p.Phe960=
XM_011519023.1:c.2862T>C	XP_011517325.1:p.Phe954=
XM_011519024.1:c.2805T>C	XP_011517326.1:p.Phe935=
XM_011519025.1:c.2781T>C	XP_011517327.1:p.Phe927=
XM_011519026.1:c.2739T>C	XP_011517328.1:p.Phe913=
XM_011519029.1:c.1305T>C	XP_011517331.1:p.Phe435=
XM_011519030.1:c.657T>C	XP_011517332.1:p.Phe219=
XM_011519031.1:c.444T>C	XP_011517333.1:p.Phe148=
XM_011519032.1:c.444T>C	XP_011517334.1:p.Phe148=
XM_011519033.1:c.2718T>C	XP_011517335.1:p.Phe906=
NM_001354263.1:c.2853T>C	NP_001341192.1:p.Phe951=
XM_005266105.5:c.2865T>C	XP_005266162.1:p.Phe955=
XM_011519021.3:c.2883T>C	XP_011517323.1:p.Phe961=
XM_011519022.3:c.2880T>C	XP_011517324.1:p.Phe960=
XM_011519023.3:c.2862T>C	XP_011517325.1:p.Phe954=
XM_011519029.3:c.1305T>C	XP_011517331.1:p.Phe435=
XM_011519030.3:c.657T>C	XP_011517332.1:p.Phe219=
XM_017015134.1:c.2859T>C	XP_016870623.1:p.Phe953=
XM_017015136.2:c.2775T>C	XP_016870625.1:p.Phe925=
XM_017015137.1:c.2760T>C	XP_016870626.1:p.Phe920=
XM_017015138.1:c.2760T>C	XP_016870627.1:p.Phe920=
XM_024447674.1:c.2703T>C	XP_024303442.1:p.Phe901=
XM_024447675.1:c.2637T>C	XP_024303443.1:p.Phe879=
XM_024447676.1:c.1998T>C	XP_024303444.1:p.Phe666=
XM_024447677.1:c.1998T>C	XP_024303445.1:p.Phe666=
XM_024447680.1:c.2616T>C	XP_024303448.1:p.Phe872=
NM_024757.5:c.2874T>C MANE Select	NP_079033.4:p.Phe958=
NM_001354263.2:c.2853T>C	NP_001341192.1:p.Phe951=