Canonical Allele Identifier: CA375794442

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707944T>A (hg19) ; chr9:g.137813492T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813492T>A , CM000671.2:g.137813492T>A	GRCh38
NC_000009.11:g.140707944T>A , CM000671.1:g.140707944T>A	GRCh37
NC_000009.10:g.139827765T>A	NCBI36
NG_011776.1:g.199501T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3142T>A MANE Select	ENSP00000417980.1:p.Ser1048Thr
ENST00000637161.1:c.3049T>A	ENSP00000490328.1:p.Ser1017Thr
ENST00000637261.1:c.3182T>A	ENSP00000490815.1:n.3182T>A
ENST00000637891.1:c.1036T>A	ENSP00000490907.1:p.Ser346Thr
ENST00000460843.5:c.3142T>A	ENSP00000417980.1:p.Ser1048Thr
ENST00000462942.3:c.1999T>A	ENSP00000436107.1:p.Ser667Thr
ENST00000483653.1:n.2T>A
ENST00000488242.2:n.668T>A
NM_024757.4:c.3142T>A	NP_079033.4:p.Ser1048Thr
XM_005266105.3:c.3133T>A	XP_005266162.1:p.Ser1045Thr
XM_005266110.1:c.3049T>A	XP_005266167.1:p.Ser1017Thr
XM_006717288.2:c.3124T>A	XP_006717351.1:p.Ser1042Thr
XM_011519021.1:c.3151T>A	XP_011517323.1:p.Ser1051Thr
XM_011519022.1:c.3148T>A	XP_011517324.1:p.Ser1050Thr
XM_011519023.1:c.3130T>A	XP_011517325.1:p.Ser1044Thr
XM_011519024.1:c.3073T>A	XP_011517326.1:p.Ser1025Thr
XM_011519025.1:c.3049T>A	XP_011517327.1:p.Ser1017Thr
XM_011519026.1:c.3007T>A	XP_011517328.1:p.Ser1003Thr
XM_011519029.1:c.1573T>A	XP_011517331.1:p.Ser525Thr
XM_011519030.1:c.925T>A	XP_011517332.1:p.Ser309Thr
XM_011519031.1:c.712T>A	XP_011517333.1:p.Ser238Thr
XM_011519032.1:c.712T>A	XP_011517334.1:p.Ser238Thr
XM_011519033.1:c.2986T>A	XP_011517335.1:p.Ser996Thr
NM_001354263.1:c.3121T>A	NP_001341192.1:p.Ser1041Thr
XM_005266105.5:c.3133T>A	XP_005266162.1:p.Ser1045Thr
XM_011519021.3:c.3151T>A	XP_011517323.1:p.Ser1051Thr
XM_011519022.3:c.3148T>A	XP_011517324.1:p.Ser1050Thr
XM_011519023.3:c.3130T>A	XP_011517325.1:p.Ser1044Thr
XM_011519029.3:c.1573T>A	XP_011517331.1:p.Ser525Thr
XM_011519030.3:c.925T>A	XP_011517332.1:p.Ser309Thr
XM_017015134.1:c.3127T>A	XP_016870623.1:p.Ser1043Thr
XM_017015136.2:c.3043T>A	XP_016870625.1:p.Ser1015Thr
XM_017015137.1:c.3028T>A	XP_016870626.1:p.Ser1010Thr
XM_017015138.1:c.3028T>A	XP_016870627.1:p.Ser1010Thr
XM_024447674.1:c.2971T>A	XP_024303442.1:p.Ser991Thr
XM_024447675.1:c.2905T>A	XP_024303443.1:p.Ser969Thr
XM_024447676.1:c.2266T>A	XP_024303444.1:p.Ser756Thr
XM_024447677.1:c.2266T>A	XP_024303445.1:p.Ser756Thr
XM_024447680.1:c.2884T>A	XP_024303448.1:p.Ser962Thr
NM_024757.5:c.3142T>A MANE Select	NP_079033.4:p.Ser1048Thr
NM_001354263.2:c.3121T>A	NP_001341192.1:p.Ser1041Thr