Canonical Allele Identifier: CA375794377

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707932A>T (hg19) ; chr9:g.137813480A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813480A>T , CM000671.2:g.137813480A>T	GRCh38
NC_000009.11:g.140707932A>T , CM000671.1:g.140707932A>T	GRCh37
NC_000009.10:g.139827753A>T	NCBI36
NG_011776.1:g.199489A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3130A>T MANE Select	ENSP00000417980.1:p.Asn1044Tyr
ENST00000637161.1:c.3037A>T	ENSP00000490328.1:p.Asn1013Tyr
ENST00000637261.1:c.3170A>T	ENSP00000490815.1:n.3170A>T
ENST00000637891.1:c.1024A>T	ENSP00000490907.1:p.Asn342Tyr
ENST00000460843.5:c.3130A>T	ENSP00000417980.1:p.Asn1044Tyr
ENST00000462942.3:c.1987A>T	ENSP00000436107.1:p.Asn663Tyr
ENST00000488242.2:n.656A>T
NM_024757.4:c.3130A>T	NP_079033.4:p.Asn1044Tyr
XM_005266105.3:c.3121A>T	XP_005266162.1:p.Asn1041Tyr
XM_005266110.1:c.3037A>T	XP_005266167.1:p.Asn1013Tyr
XM_006717288.2:c.3112A>T	XP_006717351.1:p.Asn1038Tyr
XM_011519021.1:c.3139A>T	XP_011517323.1:p.Asn1047Tyr
XM_011519022.1:c.3136A>T	XP_011517324.1:p.Asn1046Tyr
XM_011519023.1:c.3118A>T	XP_011517325.1:p.Asn1040Tyr
XM_011519024.1:c.3061A>T	XP_011517326.1:p.Asn1021Tyr
XM_011519025.1:c.3037A>T	XP_011517327.1:p.Asn1013Tyr
XM_011519026.1:c.2995A>T	XP_011517328.1:p.Asn999Tyr
XM_011519029.1:c.1561A>T	XP_011517331.1:p.Asn521Tyr
XM_011519030.1:c.913A>T	XP_011517332.1:p.Asn305Tyr
XM_011519031.1:c.700A>T	XP_011517333.1:p.Asn234Tyr
XM_011519032.1:c.700A>T	XP_011517334.1:p.Asn234Tyr
XM_011519033.1:c.2974A>T	XP_011517335.1:p.Asn992Tyr
NM_001354263.1:c.3109A>T	NP_001341192.1:p.Asn1037Tyr
XM_005266105.5:c.3121A>T	XP_005266162.1:p.Asn1041Tyr
XM_011519021.3:c.3139A>T	XP_011517323.1:p.Asn1047Tyr
XM_011519022.3:c.3136A>T	XP_011517324.1:p.Asn1046Tyr
XM_011519023.3:c.3118A>T	XP_011517325.1:p.Asn1040Tyr
XM_011519029.3:c.1561A>T	XP_011517331.1:p.Asn521Tyr
XM_011519030.3:c.913A>T	XP_011517332.1:p.Asn305Tyr
XM_017015134.1:c.3115A>T	XP_016870623.1:p.Asn1039Tyr
XM_017015136.2:c.3031A>T	XP_016870625.1:p.Asn1011Tyr
XM_017015137.1:c.3016A>T	XP_016870626.1:p.Asn1006Tyr
XM_017015138.1:c.3016A>T	XP_016870627.1:p.Asn1006Tyr
XM_024447674.1:c.2959A>T	XP_024303442.1:p.Asn987Tyr
XM_024447675.1:c.2893A>T	XP_024303443.1:p.Asn965Tyr
XM_024447676.1:c.2254A>T	XP_024303444.1:p.Asn752Tyr
XM_024447677.1:c.2254A>T	XP_024303445.1:p.Asn752Tyr
XM_024447680.1:c.2872A>T	XP_024303448.1:p.Asn958Tyr
NM_024757.5:c.3130A>T MANE Select	NP_079033.4:p.Asn1044Tyr
NM_001354263.2:c.3109A>T	NP_001341192.1:p.Asn1037Tyr