Canonical Allele Identifier: CA375793950

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707873C>G (hg19) ; chr9:g.137813421C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813421C>G , CM000671.2:g.137813421C>G	GRCh38
NC_000009.11:g.140707873C>G , CM000671.1:g.140707873C>G	GRCh37
NC_000009.10:g.139827694C>G	NCBI36
NG_011776.1:g.199430C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3071C>G MANE Select	ENSP00000417980.1:p.Pro1024Arg
ENST00000637161.1:c.2978C>G	ENSP00000490328.1:p.Pro993Arg
ENST00000637261.1:c.3111C>G	ENSP00000490815.1:n.3111C>G
ENST00000637891.1:c.965C>G	ENSP00000490907.1:p.Pro322Arg
ENST00000460843.5:c.3071C>G	ENSP00000417980.1:p.Pro1024Arg
ENST00000462942.3:c.1928C>G	ENSP00000436107.1:p.Pro643Arg
ENST00000486164.5:c.758C>G
ENST00000488242.2:n.597C>G
NM_024757.4:c.3071C>G	NP_079033.4:p.Pro1024Arg
XM_005266105.3:c.3062C>G	XP_005266162.1:p.Pro1021Arg
XM_005266110.1:c.2978C>G	XP_005266167.1:p.Pro993Arg
XM_006717288.2:c.3053C>G	XP_006717351.1:p.Pro1018Arg
XM_011519021.1:c.3080C>G	XP_011517323.1:p.Pro1027Arg
XM_011519022.1:c.3077C>G	XP_011517324.1:p.Pro1026Arg
XM_011519023.1:c.3059C>G	XP_011517325.1:p.Pro1020Arg
XM_011519024.1:c.3002C>G	XP_011517326.1:p.Pro1001Arg
XM_011519025.1:c.2978C>G	XP_011517327.1:p.Pro993Arg
XM_011519026.1:c.2936C>G	XP_011517328.1:p.Pro979Arg
XM_011519029.1:c.1502C>G	XP_011517331.1:p.Pro501Arg
XM_011519030.1:c.854C>G	XP_011517332.1:p.Pro285Arg
XM_011519031.1:c.641C>G	XP_011517333.1:p.Pro214Arg
XM_011519032.1:c.641C>G	XP_011517334.1:p.Pro214Arg
XM_011519033.1:c.2915C>G	XP_011517335.1:p.Pro972Arg
NM_001354263.1:c.3050C>G	NP_001341192.1:p.Pro1017Arg
XM_005266105.5:c.3062C>G	XP_005266162.1:p.Pro1021Arg
XM_011519021.3:c.3080C>G	XP_011517323.1:p.Pro1027Arg
XM_011519022.3:c.3077C>G	XP_011517324.1:p.Pro1026Arg
XM_011519023.3:c.3059C>G	XP_011517325.1:p.Pro1020Arg
XM_011519029.3:c.1502C>G	XP_011517331.1:p.Pro501Arg
XM_011519030.3:c.854C>G	XP_011517332.1:p.Pro285Arg
XM_017015134.1:c.3056C>G	XP_016870623.1:p.Pro1019Arg
XM_017015136.2:c.2972C>G	XP_016870625.1:p.Pro991Arg
XM_017015137.1:c.2957C>G	XP_016870626.1:p.Pro986Arg
XM_017015138.1:c.2957C>G	XP_016870627.1:p.Pro986Arg
XM_024447674.1:c.2900C>G	XP_024303442.1:p.Pro967Arg
XM_024447675.1:c.2834C>G	XP_024303443.1:p.Pro945Arg
XM_024447676.1:c.2195C>G	XP_024303444.1:p.Pro732Arg
XM_024447677.1:c.2195C>G	XP_024303445.1:p.Pro732Arg
XM_024447680.1:c.2813C>G	XP_024303448.1:p.Pro938Arg
NM_024757.5:c.3071C>G MANE Select	NP_079033.4:p.Pro1024Arg
NM_001354263.2:c.3050C>G	NP_001341192.1:p.Pro1017Arg