Canonical Allele Identifier: CA1884685910

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813482C= , CM000671.2:g.137813482C=	GRCh38
NC_000009.11:g.140707934C= , CM000671.1:g.140707934C=	GRCh37
NC_000009.10:g.139827755C=	NCBI36
NG_011776.1:g.199491C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3132C= MANE Select	ENSP00000417980.1:p.Asn1044=
ENST00000637161.1:c.3039C=	ENSP00000490328.1:p.Asn1013=
ENST00000637261.1:c.3172C=	ENSP00000490815.1:n.3172C=
ENST00000637891.1:c.1026C=	ENSP00000490907.1:p.Asn342=
ENST00000460843.5:c.3132C=	ENSP00000417980.1:p.Asn1044=
ENST00000462942.3:c.1989C=	ENSP00000436107.1:p.Asn663=
ENST00000488242.2:n.658C=
NM_024757.4:c.3132C=	NP_079033.4:p.Asn1044=
XM_005266105.3:c.3123C=	XP_005266162.1:p.Asn1041=
XM_005266110.1:c.3039C=	XP_005266167.1:p.Asn1013=
XM_006717288.2:c.3114C=	XP_006717351.1:p.Asn1038=
XM_011519021.1:c.3141C=	XP_011517323.1:p.Asn1047=
XM_011519022.1:c.3138C=	XP_011517324.1:p.Asn1046=
XM_011519023.1:c.3120C=	XP_011517325.1:p.Asn1040=
XM_011519024.1:c.3063C=	XP_011517326.1:p.Asn1021=
XM_011519025.1:c.3039C=	XP_011517327.1:p.Asn1013=
XM_011519026.1:c.2997C=	XP_011517328.1:p.Asn999=
XM_011519029.1:c.1563C=	XP_011517331.1:p.Asn521=
XM_011519030.1:c.915C=	XP_011517332.1:p.Asn305=
XM_011519031.1:c.702C=	XP_011517333.1:p.Asn234=
XM_011519032.1:c.702C=	XP_011517334.1:p.Asn234=
XM_011519033.1:c.2976C=	XP_011517335.1:p.Asn992=
NM_001354263.1:c.3111C=	NP_001341192.1:p.Asn1037=
XM_005266105.5:c.3123C=	XP_005266162.1:p.Asn1041=
XM_011519021.3:c.3141C=	XP_011517323.1:p.Asn1047=
XM_011519022.3:c.3138C=	XP_011517324.1:p.Asn1046=
XM_011519023.3:c.3120C=	XP_011517325.1:p.Asn1040=
XM_011519029.3:c.1563C=	XP_011517331.1:p.Asn521=
XM_011519030.3:c.915C=	XP_011517332.1:p.Asn305=
XM_017015134.1:c.3117C=	XP_016870623.1:p.Asn1039=
XM_017015136.2:c.3033C=	XP_016870625.1:p.Asn1011=
XM_017015137.1:c.3018C=	XP_016870626.1:p.Asn1006=
XM_017015138.1:c.3018C=	XP_016870627.1:p.Asn1006=
XM_024447674.1:c.2961C=	XP_024303442.1:p.Asn987=
XM_024447675.1:c.2895C=	XP_024303443.1:p.Asn965=
XM_024447676.1:c.2256C=	XP_024303444.1:p.Asn752=
XM_024447677.1:c.2256C=	XP_024303445.1:p.Asn752=
XM_024447680.1:c.2874C=	XP_024303448.1:p.Asn958=
NM_024757.5:c.3132C= MANE Select	NP_079033.4:p.Asn1044=
NM_001354263.2:c.3111C=	NP_001341192.1:p.Asn1037=