Canonical Allele Identifier: CA375794554

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707964A>C (hg19) ; chr9:g.137813512A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813512A>C , CM000671.2:g.137813512A>C	GRCh38
NC_000009.11:g.140707964A>C , CM000671.1:g.140707964A>C	GRCh37
NC_000009.10:g.139827785A>C	NCBI36
NG_011776.1:g.199521A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3162A>C MANE Select	ENSP00000417980.1:p.Arg1054Ser
ENST00000637161.1:c.3069A>C	ENSP00000490328.1:p.Arg1023Ser
ENST00000637261.1:c.3202A>C	ENSP00000490815.1:n.3202A>C
ENST00000637891.1:c.1056A>C	ENSP00000490907.1:p.Arg352Ser
ENST00000460843.5:c.3162A>C	ENSP00000417980.1:p.Arg1054Ser
ENST00000462942.3:c.2019A>C	ENSP00000436107.1:p.Arg673Ser
ENST00000483653.1:n.22A>C
ENST00000488242.2:n.688A>C
NM_024757.4:c.3162A>C	NP_079033.4:p.Arg1054Ser
XM_005266105.3:c.3153A>C	XP_005266162.1:p.Arg1051Ser
XM_005266110.1:c.3069A>C	XP_005266167.1:p.Arg1023Ser
XM_006717288.2:c.3144A>C	XP_006717351.1:p.Arg1048Ser
XM_011519021.1:c.3171A>C	XP_011517323.1:p.Arg1057Ser
XM_011519022.1:c.3168A>C	XP_011517324.1:p.Arg1056Ser
XM_011519023.1:c.3150A>C	XP_011517325.1:p.Arg1050Ser
XM_011519024.1:c.3093A>C	XP_011517326.1:p.Arg1031Ser
XM_011519025.1:c.3069A>C	XP_011517327.1:p.Arg1023Ser
XM_011519026.1:c.3027A>C	XP_011517328.1:p.Arg1009Ser
XM_011519029.1:c.1593A>C	XP_011517331.1:p.Arg531Ser
XM_011519030.1:c.945A>C	XP_011517332.1:p.Arg315Ser
XM_011519031.1:c.732A>C	XP_011517333.1:p.Arg244Ser
XM_011519032.1:c.732A>C	XP_011517334.1:p.Arg244Ser
XM_011519033.1:c.3006A>C	XP_011517335.1:p.Arg1002Ser
NM_001354263.1:c.3141A>C	NP_001341192.1:p.Arg1047Ser
XM_005266105.5:c.3153A>C	XP_005266162.1:p.Arg1051Ser
XM_011519021.3:c.3171A>C	XP_011517323.1:p.Arg1057Ser
XM_011519022.3:c.3168A>C	XP_011517324.1:p.Arg1056Ser
XM_011519023.3:c.3150A>C	XP_011517325.1:p.Arg1050Ser
XM_011519029.3:c.1593A>C	XP_011517331.1:p.Arg531Ser
XM_011519030.3:c.945A>C	XP_011517332.1:p.Arg315Ser
XM_017015134.1:c.3147A>C	XP_016870623.1:p.Arg1049Ser
XM_017015136.2:c.3063A>C	XP_016870625.1:p.Arg1021Ser
XM_017015137.1:c.3048A>C	XP_016870626.1:p.Arg1016Ser
XM_017015138.1:c.3048A>C	XP_016870627.1:p.Arg1016Ser
XM_024447674.1:c.2991A>C	XP_024303442.1:p.Arg997Ser
XM_024447675.1:c.2925A>C	XP_024303443.1:p.Arg975Ser
XM_024447676.1:c.2286A>C	XP_024303444.1:p.Arg762Ser
XM_024447677.1:c.2286A>C	XP_024303445.1:p.Arg762Ser
XM_024447680.1:c.2904A>C	XP_024303448.1:p.Arg968Ser
NM_024757.5:c.3162A>C MANE Select	NP_079033.4:p.Arg1054Ser
NM_001354263.2:c.3141A>C	NP_001341192.1:p.Arg1047Ser