Canonical Allele Identifier: CA2626946434

Gene: TMEM121

Linked Data

• gnomAD v4: 14-105529729-C-CCGA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.105529731_105529732insACG , CM000676.2:g.105529731_105529732insACG	GRCh38
NC_000014.8:g.105996068_105996069insACG , CM000676.1:g.105996068_105996069insACG	GRCh37
NC_000014.7:g.105067113_105067114insACG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392519.7:c.897_898insACG MANE Select	ENSP00000376304.2:p.Pro299_Leu300insThr
ENST00000392519.6:c.897_898insACG	ENSP00000376304.2:p.Pro299_Leu300insThr
ENST00000431372.1:c.897_898insACG	ENSP00000407456.1:p.Pro299_Leu300insThr
NM_025268.2:c.897_898insACG	NP_079544.1:p.Pro299_Leu300insThr
XM_005268101.2:c.897_898insACG	XP_005268158.1:p.Pro299_Leu300insThr
XM_006720261.2:c.897_898insACG	XP_006720324.1:p.Pro299_Leu300insThr
XM_011537185.1:c.897_898insACG	XP_011535487.1:p.Pro299_Leu300insThr
XM_011537186.1:c.897_898insACG	XP_011535488.1:p.Pro299_Leu300insThr
NM_001331238.1:c.897_898insACG	NP_001318167.1:p.Pro299_Leu300insThr
NM_025268.3:c.897_898insACG	NP_079544.1:p.Pro299_Leu300insThr
XM_006720261.3:c.897_898insACG	XP_006720324.1:p.Pro299_Leu300insThr
NM_025268.4:c.897_898insACG MANE Select	NP_079544.1:p.Pro299_Leu300insThr
NM_001331238.2:c.897_898insACG	NP_001318167.1:p.Pro299_Leu300insThr