Canonical Allele Identifier: CA2626946380

Gene: TMEM121

Linked Data

• gnomAD v4: 14-105529720-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.105529720_105529721insTT , CM000676.2:g.105529720_105529721insTT	GRCh38
NC_000014.8:g.105996057_105996058insTT , CM000676.1:g.105996057_105996058insTT	GRCh37
NC_000014.7:g.105067102_105067103insTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392519.7:c.886_887insTT MANE Select	ENSP00000376304.2:p.Pro296LeufsTer?
ENST00000392519.6:c.886_887insTT	ENSP00000376304.2:p.Pro296LeufsTer?
ENST00000431372.1:c.886_887insTT	ENSP00000407456.1:p.Pro296LeufsTer?
NM_025268.2:c.886_887insTT	NP_079544.1:p.Pro296LeufsTer?
XM_005268101.2:c.886_887insTT	XP_005268158.1:p.Pro296LeufsTer?
XM_006720261.2:c.886_887insTT	XP_006720324.1:p.Pro296LeufsTer?
XM_011537185.1:c.886_887insTT	XP_011535487.1:p.Pro296LeufsTer?
XM_011537186.1:c.886_887insTT	XP_011535488.1:p.Pro296LeufsTer?
NM_001331238.1:c.886_887insTT	NP_001318167.1:p.Pro296LeufsTer?
NM_025268.3:c.886_887insTT	NP_079544.1:p.Pro296LeufsTer?
XM_006720261.3:c.886_887insTT	XP_006720324.1:p.Pro296LeufsTer?
NM_025268.4:c.886_887insTT MANE Select	NP_079544.1:p.Pro296LeufsTer?
NM_001331238.2:c.886_887insTT	NP_001318167.1:p.Pro296LeufsTer?