Canonical Allele Identifier: CA375789033

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695423A>C (hg19) ; chr9:g.137800971A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800971A>C , CM000671.2:g.137800971A>C	GRCh38
NC_000009.11:g.140695423A>C , CM000671.1:g.140695423A>C	GRCh37
NC_000009.10:g.139815244A>C	NCBI36
NG_011776.1:g.186980A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2699A>C MANE Select	ENSP00000417980.1:p.Asn900Thr
ENST00000636027.1:c.2585A>C	ENSP00000489961.1:p.Asn862Thr
ENST00000637161.1:c.2606A>C	ENSP00000490328.1:p.Asn869Thr
ENST00000637261.1:c.2739A>C	ENSP00000490815.1:n.2739A>C
ENST00000637891.1:c.593A>C	ENSP00000490907.1:p.Asn198Thr
ENST00000637949.1:c.377A>C	ENSP00000489786.1:p.Asn126Thr
ENST00000460843.5:c.2699A>C	ENSP00000417980.1:p.Asn900Thr
ENST00000462942.3:c.1556A>C	ENSP00000436107.1:p.Asn519Thr
ENST00000482340.5:c.269A>C	ENSP00000486748.1:p.Asn90Thr
ENST00000486164.5:c.277A>C
ENST00000488242.2:n.225A>C
ENST00000493484.5:c.269A>C	ENSP00000486503.1:p.Asn90Thr
NM_024757.4:c.2699A>C	NP_079033.4:p.Asn900Thr
XM_005266105.3:c.2690A>C	XP_005266162.1:p.Asn897Thr
XM_005266110.1:c.2606A>C	XP_005266167.1:p.Asn869Thr
XM_006717288.2:c.2681A>C	XP_006717351.1:p.Asn894Thr
XM_011519021.1:c.2708A>C	XP_011517323.1:p.Asn903Thr
XM_011519022.1:c.2705A>C	XP_011517324.1:p.Asn902Thr
XM_011519023.1:c.2687A>C	XP_011517325.1:p.Asn896Thr
XM_011519024.1:c.2630A>C	XP_011517326.1:p.Asn877Thr
XM_011519025.1:c.2606A>C	XP_011517327.1:p.Asn869Thr
XM_011519026.1:c.2564A>C	XP_011517328.1:p.Asn855Thr
XM_011519027.1:c.2708A>C	XP_011517329.1:p.Asn903Thr
XM_011519029.1:c.1130A>C	XP_011517331.1:p.Asn377Thr
XM_011519030.1:c.482A>C	XP_011517332.1:p.Asn161Thr
XM_011519031.1:c.269A>C	XP_011517333.1:p.Asn90Thr
XM_011519032.1:c.269A>C	XP_011517334.1:p.Asn90Thr
XM_011519033.1:c.2543A>C	XP_011517335.1:p.Asn848Thr
NM_001354263.1:c.2678A>C	NP_001341192.1:p.Asn893Thr
XM_005266105.5:c.2690A>C	XP_005266162.1:p.Asn897Thr
XM_011519021.3:c.2708A>C	XP_011517323.1:p.Asn903Thr
XM_011519022.3:c.2705A>C	XP_011517324.1:p.Asn902Thr
XM_011519023.3:c.2687A>C	XP_011517325.1:p.Asn896Thr
XM_011519029.3:c.1130A>C	XP_011517331.1:p.Asn377Thr
XM_011519030.3:c.482A>C	XP_011517332.1:p.Asn161Thr
XM_017015134.1:c.2684A>C	XP_016870623.1:p.Asn895Thr
XM_017015136.2:c.2600A>C	XP_016870625.1:p.Asn867Thr
XM_017015137.1:c.2585A>C	XP_016870626.1:p.Asn862Thr
XM_017015138.1:c.2585A>C	XP_016870627.1:p.Asn862Thr
XM_024447674.1:c.2528A>C	XP_024303442.1:p.Asn843Thr
XM_024447675.1:c.2462A>C	XP_024303443.1:p.Asn821Thr
XM_024447676.1:c.1823A>C	XP_024303444.1:p.Asn608Thr
XM_024447677.1:c.1823A>C	XP_024303445.1:p.Asn608Thr
XM_024447678.1:c.2606A>C	XP_024303446.1:p.Asn869Thr
XM_024447680.1:c.2441A>C	XP_024303448.1:p.Asn814Thr
NM_024757.5:c.2699A>C MANE Select	NP_079033.4:p.Asn900Thr
NM_001354263.2:c.2678A>C	NP_001341192.1:p.Asn893Thr