Canonical Allele Identifier: CA375794362

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707930A>T (hg19) ; chr9:g.137813478A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813478A>T , CM000671.2:g.137813478A>T	GRCh38
NC_000009.11:g.140707930A>T , CM000671.1:g.140707930A>T	GRCh37
NC_000009.10:g.139827751A>T	NCBI36
NG_011776.1:g.199487A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3128A>T MANE Select	ENSP00000417980.1:p.Gln1043Leu
ENST00000637161.1:c.3035A>T	ENSP00000490328.1:p.Gln1012Leu
ENST00000637261.1:c.3168A>T	ENSP00000490815.1:n.3168A>T
ENST00000637891.1:c.1022A>T	ENSP00000490907.1:p.Gln341Leu
ENST00000460843.5:c.3128A>T	ENSP00000417980.1:p.Gln1043Leu
ENST00000462942.3:c.1985A>T	ENSP00000436107.1:p.Gln662Leu
ENST00000488242.2:n.654A>T
NM_024757.4:c.3128A>T	NP_079033.4:p.Gln1043Leu
XM_005266105.3:c.3119A>T	XP_005266162.1:p.Gln1040Leu
XM_005266110.1:c.3035A>T	XP_005266167.1:p.Gln1012Leu
XM_006717288.2:c.3110A>T	XP_006717351.1:p.Gln1037Leu
XM_011519021.1:c.3137A>T	XP_011517323.1:p.Gln1046Leu
XM_011519022.1:c.3134A>T	XP_011517324.1:p.Gln1045Leu
XM_011519023.1:c.3116A>T	XP_011517325.1:p.Gln1039Leu
XM_011519024.1:c.3059A>T	XP_011517326.1:p.Gln1020Leu
XM_011519025.1:c.3035A>T	XP_011517327.1:p.Gln1012Leu
XM_011519026.1:c.2993A>T	XP_011517328.1:p.Gln998Leu
XM_011519029.1:c.1559A>T	XP_011517331.1:p.Gln520Leu
XM_011519030.1:c.911A>T	XP_011517332.1:p.Gln304Leu
XM_011519031.1:c.698A>T	XP_011517333.1:p.Gln233Leu
XM_011519032.1:c.698A>T	XP_011517334.1:p.Gln233Leu
XM_011519033.1:c.2972A>T	XP_011517335.1:p.Gln991Leu
NM_001354263.1:c.3107A>T	NP_001341192.1:p.Gln1036Leu
XM_005266105.5:c.3119A>T	XP_005266162.1:p.Gln1040Leu
XM_011519021.3:c.3137A>T	XP_011517323.1:p.Gln1046Leu
XM_011519022.3:c.3134A>T	XP_011517324.1:p.Gln1045Leu
XM_011519023.3:c.3116A>T	XP_011517325.1:p.Gln1039Leu
XM_011519029.3:c.1559A>T	XP_011517331.1:p.Gln520Leu
XM_011519030.3:c.911A>T	XP_011517332.1:p.Gln304Leu
XM_017015134.1:c.3113A>T	XP_016870623.1:p.Gln1038Leu
XM_017015136.2:c.3029A>T	XP_016870625.1:p.Gln1010Leu
XM_017015137.1:c.3014A>T	XP_016870626.1:p.Gln1005Leu
XM_017015138.1:c.3014A>T	XP_016870627.1:p.Gln1005Leu
XM_024447674.1:c.2957A>T	XP_024303442.1:p.Gln986Leu
XM_024447675.1:c.2891A>T	XP_024303443.1:p.Gln964Leu
XM_024447676.1:c.2252A>T	XP_024303444.1:p.Gln751Leu
XM_024447677.1:c.2252A>T	XP_024303445.1:p.Gln751Leu
XM_024447680.1:c.2870A>T	XP_024303448.1:p.Gln957Leu
NM_024757.5:c.3128A>T MANE Select	NP_079033.4:p.Gln1043Leu
NM_001354263.2:c.3107A>T	NP_001341192.1:p.Gln1036Leu