Canonical Allele Identifier: CA375793277

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707487C>G (hg19) ; chr9:g.137813035C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813035C>G , CM000671.2:g.137813035C>G	GRCh38
NC_000009.11:g.140707487C>G , CM000671.1:g.140707487C>G	GRCh37
NC_000009.10:g.139827308C>G	NCBI36
NG_011776.1:g.199044C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2897C>G MANE Select	ENSP00000417980.1:p.Thr966Ser
ENST00000636027.1:c.2783C>G	ENSP00000489961.1:p.Thr928Ser
ENST00000637161.1:c.2804C>G	ENSP00000490328.1:p.Thr935Ser
ENST00000637261.1:c.2937C>G	ENSP00000490815.1:n.2937C>G
ENST00000637891.1:c.791C>G	ENSP00000490907.1:p.Thr264Ser
ENST00000460843.5:c.2897C>G	ENSP00000417980.1:p.Thr966Ser
ENST00000462942.3:c.1754C>G	ENSP00000436107.1:p.Thr585Ser
ENST00000486164.5:c.584C>G
ENST00000488242.2:n.423C>G
NM_024757.4:c.2897C>G	NP_079033.4:p.Thr966Ser
XM_005266105.3:c.2888C>G	XP_005266162.1:p.Thr963Ser
XM_005266110.1:c.2804C>G	XP_005266167.1:p.Thr935Ser
XM_006717288.2:c.2879C>G	XP_006717351.1:p.Thr960Ser
XM_011519021.1:c.2906C>G	XP_011517323.1:p.Thr969Ser
XM_011519022.1:c.2903C>G	XP_011517324.1:p.Thr968Ser
XM_011519023.1:c.2885C>G	XP_011517325.1:p.Thr962Ser
XM_011519024.1:c.2828C>G	XP_011517326.1:p.Thr943Ser
XM_011519025.1:c.2804C>G	XP_011517327.1:p.Thr935Ser
XM_011519026.1:c.2762C>G	XP_011517328.1:p.Thr921Ser
XM_011519029.1:c.1328C>G	XP_011517331.1:p.Thr443Ser
XM_011519030.1:c.680C>G	XP_011517332.1:p.Thr227Ser
XM_011519031.1:c.467C>G	XP_011517333.1:p.Thr156Ser
XM_011519032.1:c.467C>G	XP_011517334.1:p.Thr156Ser
XM_011519033.1:c.2741C>G	XP_011517335.1:p.Thr914Ser
NM_001354263.1:c.2876C>G	NP_001341192.1:p.Thr959Ser
XM_005266105.5:c.2888C>G	XP_005266162.1:p.Thr963Ser
XM_011519021.3:c.2906C>G	XP_011517323.1:p.Thr969Ser
XM_011519022.3:c.2903C>G	XP_011517324.1:p.Thr968Ser
XM_011519023.3:c.2885C>G	XP_011517325.1:p.Thr962Ser
XM_011519029.3:c.1328C>G	XP_011517331.1:p.Thr443Ser
XM_011519030.3:c.680C>G	XP_011517332.1:p.Thr227Ser
XM_017015134.1:c.2882C>G	XP_016870623.1:p.Thr961Ser
XM_017015136.2:c.2798C>G	XP_016870625.1:p.Thr933Ser
XM_017015137.1:c.2783C>G	XP_016870626.1:p.Thr928Ser
XM_017015138.1:c.2783C>G	XP_016870627.1:p.Thr928Ser
XM_024447674.1:c.2726C>G	XP_024303442.1:p.Thr909Ser
XM_024447675.1:c.2660C>G	XP_024303443.1:p.Thr887Ser
XM_024447676.1:c.2021C>G	XP_024303444.1:p.Thr674Ser
XM_024447677.1:c.2021C>G	XP_024303445.1:p.Thr674Ser
XM_024447680.1:c.2639C>G	XP_024303448.1:p.Thr880Ser
NM_024757.5:c.2897C>G MANE Select	NP_079033.4:p.Thr966Ser
NM_001354263.2:c.2876C>G	NP_001341192.1:p.Thr959Ser