Canonical Allele Identifier: CA375794358
Gene: EHMT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137813478A>C , CM000671.2:g.137813478A>C GRCh38
NC_000009.11:g.140707930A>C , CM000671.1:g.140707930A>C GRCh37
NC_000009.10:g.139827751A>C NCBI36
NG_011776.1:g.199487A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.3128A>C MANE Select ENSP00000417980.1:p.Gln1043Pro
ENST00000637161.1:c.3035A>C ENSP00000490328.1:p.Gln1012Pro
ENST00000637261.1:c.3168A>C ENSP00000490815.1:n.3168A>C
ENST00000637891.1:c.1022A>C ENSP00000490907.1:p.Gln341Pro
ENST00000460843.5:c.3128A>C ENSP00000417980.1:p.Gln1043Pro
ENST00000462942.3:c.1985A>C ENSP00000436107.1:p.Gln662Pro
ENST00000488242.2:n.654A>C
NM_024757.4:c.3128A>C NP_079033.4:p.Gln1043Pro
XM_005266105.3:c.3119A>C XP_005266162.1:p.Gln1040Pro
XM_005266110.1:c.3035A>C XP_005266167.1:p.Gln1012Pro
XM_006717288.2:c.3110A>C XP_006717351.1:p.Gln1037Pro
XM_011519021.1:c.3137A>C XP_011517323.1:p.Gln1046Pro
XM_011519022.1:c.3134A>C XP_011517324.1:p.Gln1045Pro
XM_011519023.1:c.3116A>C XP_011517325.1:p.Gln1039Pro
XM_011519024.1:c.3059A>C XP_011517326.1:p.Gln1020Pro
XM_011519025.1:c.3035A>C XP_011517327.1:p.Gln1012Pro
XM_011519026.1:c.2993A>C XP_011517328.1:p.Gln998Pro
XM_011519029.1:c.1559A>C XP_011517331.1:p.Gln520Pro
XM_011519030.1:c.911A>C XP_011517332.1:p.Gln304Pro
XM_011519031.1:c.698A>C XP_011517333.1:p.Gln233Pro
XM_011519032.1:c.698A>C XP_011517334.1:p.Gln233Pro
XM_011519033.1:c.2972A>C XP_011517335.1:p.Gln991Pro
NM_001354263.1:c.3107A>C NP_001341192.1:p.Gln1036Pro
XM_005266105.5:c.3119A>C XP_005266162.1:p.Gln1040Pro
XM_011519021.3:c.3137A>C XP_011517323.1:p.Gln1046Pro
XM_011519022.3:c.3134A>C XP_011517324.1:p.Gln1045Pro
XM_011519023.3:c.3116A>C XP_011517325.1:p.Gln1039Pro
XM_011519029.3:c.1559A>C XP_011517331.1:p.Gln520Pro
XM_011519030.3:c.911A>C XP_011517332.1:p.Gln304Pro
XM_017015134.1:c.3113A>C XP_016870623.1:p.Gln1038Pro
XM_017015136.2:c.3029A>C XP_016870625.1:p.Gln1010Pro
XM_017015137.1:c.3014A>C XP_016870626.1:p.Gln1005Pro
XM_017015138.1:c.3014A>C XP_016870627.1:p.Gln1005Pro
XM_024447674.1:c.2957A>C XP_024303442.1:p.Gln986Pro
XM_024447675.1:c.2891A>C XP_024303443.1:p.Gln964Pro
XM_024447676.1:c.2252A>C XP_024303444.1:p.Gln751Pro
XM_024447677.1:c.2252A>C XP_024303445.1:p.Gln751Pro
XM_024447680.1:c.2870A>C XP_024303448.1:p.Gln957Pro
NM_024757.5:c.3128A>C MANE Select NP_079033.4:p.Gln1043Pro
NM_001354263.2:c.3107A>C NP_001341192.1:p.Gln1036Pro