Canonical Allele Identifier: CA375794595

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707970C>G (hg19) ; chr9:g.137813518C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813518C>G , CM000671.2:g.137813518C>G	GRCh38
NC_000009.11:g.140707970C>G , CM000671.1:g.140707970C>G	GRCh37
NC_000009.10:g.139827791C>G	NCBI36
NG_011776.1:g.199527C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3168C>G MANE Select	ENSP00000417980.1:p.Ile1056Met
ENST00000637161.1:c.3075C>G	ENSP00000490328.1:p.Ile1025Met
ENST00000637261.1:c.3208C>G	ENSP00000490815.1:n.3208C>G
ENST00000637891.1:c.1062C>G	ENSP00000490907.1:p.Ile354Met
ENST00000460843.5:c.3168C>G	ENSP00000417980.1:p.Ile1056Met
ENST00000462942.3:c.2025C>G	ENSP00000436107.1:p.Ile675Met
ENST00000483653.1:n.28C>G
ENST00000488242.2:n.694C>G
NM_024757.4:c.3168C>G	NP_079033.4:p.Ile1056Met
XM_005266105.3:c.3159C>G	XP_005266162.1:p.Ile1053Met
XM_005266110.1:c.3075C>G	XP_005266167.1:p.Ile1025Met
XM_006717288.2:c.3150C>G	XP_006717351.1:p.Ile1050Met
XM_011519021.1:c.3177C>G	XP_011517323.1:p.Ile1059Met
XM_011519022.1:c.3174C>G	XP_011517324.1:p.Ile1058Met
XM_011519023.1:c.3156C>G	XP_011517325.1:p.Ile1052Met
XM_011519024.1:c.3099C>G	XP_011517326.1:p.Ile1033Met
XM_011519025.1:c.3075C>G	XP_011517327.1:p.Ile1025Met
XM_011519026.1:c.3033C>G	XP_011517328.1:p.Ile1011Met
XM_011519029.1:c.1599C>G	XP_011517331.1:p.Ile533Met
XM_011519030.1:c.951C>G	XP_011517332.1:p.Ile317Met
XM_011519031.1:c.738C>G	XP_011517333.1:p.Ile246Met
XM_011519032.1:c.738C>G	XP_011517334.1:p.Ile246Met
XM_011519033.1:c.3012C>G	XP_011517335.1:p.Ile1004Met
NM_001354263.1:c.3147C>G	NP_001341192.1:p.Ile1049Met
XM_005266105.5:c.3159C>G	XP_005266162.1:p.Ile1053Met
XM_011519021.3:c.3177C>G	XP_011517323.1:p.Ile1059Met
XM_011519022.3:c.3174C>G	XP_011517324.1:p.Ile1058Met
XM_011519023.3:c.3156C>G	XP_011517325.1:p.Ile1052Met
XM_011519029.3:c.1599C>G	XP_011517331.1:p.Ile533Met
XM_011519030.3:c.951C>G	XP_011517332.1:p.Ile317Met
XM_017015134.1:c.3153C>G	XP_016870623.1:p.Ile1051Met
XM_017015136.2:c.3069C>G	XP_016870625.1:p.Ile1023Met
XM_017015137.1:c.3054C>G	XP_016870626.1:p.Ile1018Met
XM_017015138.1:c.3054C>G	XP_016870627.1:p.Ile1018Met
XM_024447674.1:c.2997C>G	XP_024303442.1:p.Ile999Met
XM_024447675.1:c.2931C>G	XP_024303443.1:p.Ile977Met
XM_024447676.1:c.2292C>G	XP_024303444.1:p.Ile764Met
XM_024447677.1:c.2292C>G	XP_024303445.1:p.Ile764Met
XM_024447680.1:c.2910C>G	XP_024303448.1:p.Ile970Met
NM_024757.5:c.3168C>G MANE Select	NP_079033.4:p.Ile1056Met
NM_001354263.2:c.3147C>G	NP_001341192.1:p.Ile1049Met