Canonical Allele Identifier: CA2802976012
Gene: TMEM121 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.105529678_105529683dup , CM000676.2:g.105529678_105529683dup GRCh38
NC_000014.8:g.105996015_105996020dup , CM000676.1:g.105996015_105996020dup GRCh37
NC_000014.7:g.105067060_105067065dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000392519.7:c.844_849dup MANE Select ENSP00000376304.2:p.Leu283_Gln284insGluLeu
ENST00000392519.6:c.844_849dup ENSP00000376304.2:p.Leu283_Gln284insGluLeu
ENST00000431372.1:c.844_849dup ENSP00000407456.1:p.Leu283_Gln284insGluLeu
NM_025268.2:c.844_849dup NP_079544.1:p.Leu283_Gln284insGluLeu
XM_005268101.2:c.844_849dup XP_005268158.1:p.Leu283_Gln284insGluLeu
XM_006720261.2:c.844_849dup XP_006720324.1:p.Leu283_Gln284insGluLeu
XM_011537185.1:c.844_849dup XP_011535487.1:p.Leu283_Gln284insGluLeu
XM_011537186.1:c.844_849dup XP_011535488.1:p.Leu283_Gln284insGluLeu
NM_001331238.1:c.844_849dup NP_001318167.1:p.Leu283_Gln284insGluLeu
NM_025268.3:c.844_849dup NP_079544.1:p.Leu283_Gln284insGluLeu
XM_006720261.3:c.844_849dup XP_006720324.1:p.Leu283_Gln284insGluLeu
NM_025268.4:c.844_849dup MANE Select NP_079544.1:p.Leu283_Gln284insGluLeu
NM_001331238.2:c.844_849dup NP_001318167.1:p.Leu283_Gln284insGluLeu