Canonical Allele Identifier: CA375794572

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707967T>A (hg19) ; chr9:g.137813515T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813515T>A , CM000671.2:g.137813515T>A	GRCh38
NC_000009.11:g.140707967T>A , CM000671.1:g.140707967T>A	GRCh37
NC_000009.10:g.139827788T>A	NCBI36
NG_011776.1:g.199524T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3165T>A MANE Select	ENSP00000417980.1:p.Asn1055Lys
ENST00000637161.1:c.3072T>A	ENSP00000490328.1:p.Asn1024Lys
ENST00000637261.1:c.3205T>A	ENSP00000490815.1:n.3205T>A
ENST00000637891.1:c.1059T>A	ENSP00000490907.1:p.Asn353Lys
ENST00000460843.5:c.3165T>A	ENSP00000417980.1:p.Asn1055Lys
ENST00000462942.3:c.2022T>A	ENSP00000436107.1:p.Asn674Lys
ENST00000483653.1:n.25T>A
ENST00000488242.2:n.691T>A
NM_024757.4:c.3165T>A	NP_079033.4:p.Asn1055Lys
XM_005266105.3:c.3156T>A	XP_005266162.1:p.Asn1052Lys
XM_005266110.1:c.3072T>A	XP_005266167.1:p.Asn1024Lys
XM_006717288.2:c.3147T>A	XP_006717351.1:p.Asn1049Lys
XM_011519021.1:c.3174T>A	XP_011517323.1:p.Asn1058Lys
XM_011519022.1:c.3171T>A	XP_011517324.1:p.Asn1057Lys
XM_011519023.1:c.3153T>A	XP_011517325.1:p.Asn1051Lys
XM_011519024.1:c.3096T>A	XP_011517326.1:p.Asn1032Lys
XM_011519025.1:c.3072T>A	XP_011517327.1:p.Asn1024Lys
XM_011519026.1:c.3030T>A	XP_011517328.1:p.Asn1010Lys
XM_011519029.1:c.1596T>A	XP_011517331.1:p.Asn532Lys
XM_011519030.1:c.948T>A	XP_011517332.1:p.Asn316Lys
XM_011519031.1:c.735T>A	XP_011517333.1:p.Asn245Lys
XM_011519032.1:c.735T>A	XP_011517334.1:p.Asn245Lys
XM_011519033.1:c.3009T>A	XP_011517335.1:p.Asn1003Lys
NM_001354263.1:c.3144T>A	NP_001341192.1:p.Asn1048Lys
XM_005266105.5:c.3156T>A	XP_005266162.1:p.Asn1052Lys
XM_011519021.3:c.3174T>A	XP_011517323.1:p.Asn1058Lys
XM_011519022.3:c.3171T>A	XP_011517324.1:p.Asn1057Lys
XM_011519023.3:c.3153T>A	XP_011517325.1:p.Asn1051Lys
XM_011519029.3:c.1596T>A	XP_011517331.1:p.Asn532Lys
XM_011519030.3:c.948T>A	XP_011517332.1:p.Asn316Lys
XM_017015134.1:c.3150T>A	XP_016870623.1:p.Asn1050Lys
XM_017015136.2:c.3066T>A	XP_016870625.1:p.Asn1022Lys
XM_017015137.1:c.3051T>A	XP_016870626.1:p.Asn1017Lys
XM_017015138.1:c.3051T>A	XP_016870627.1:p.Asn1017Lys
XM_024447674.1:c.2994T>A	XP_024303442.1:p.Asn998Lys
XM_024447675.1:c.2928T>A	XP_024303443.1:p.Asn976Lys
XM_024447676.1:c.2289T>A	XP_024303444.1:p.Asn763Lys
XM_024447677.1:c.2289T>A	XP_024303445.1:p.Asn763Lys
XM_024447680.1:c.2907T>A	XP_024303448.1:p.Asn969Lys
NM_024757.5:c.3165T>A MANE Select	NP_079033.4:p.Asn1055Lys
NM_001354263.2:c.3144T>A	NP_001341192.1:p.Asn1048Lys