Canonical Allele Identifier: CA2626947540

Gene: TMEM121

Linked Data

• gnomAD v4: 14-105529878-T-TGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.105529883_105529884insGGGGGG , CM000676.2:g.105529883_105529884insGGGGGG	GRCh38
NC_000014.8:g.105996220_105996221insGGGGGG , CM000676.1:g.105996220_105996221insGGGGGG	GRCh37
NC_000014.7:g.105067265_105067266insGGGGGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392519.7:c.*89_*90insGGGGGG MANE Select	ENSP00000376304.2:n.*89_*90insGGGGGG
ENST00000392519.6:c.*89_*90insGGGGGG	ENSP00000376304.2:n.*89_*90insGGGGGG
ENST00000431372.1:c.*89_*90insGGGGGG	ENSP00000407456.1:n.*89_*90insGGGGGG
NM_025268.2:c.*89_*90insGGGGGG	NP_079544.1:n.*89_*90insGGGGGG
XM_005268101.2:c.*89_*90insGGGGGG	XP_005268158.1:n.*89_*90insGGGGGG
XM_006720261.2:c.*89_*90insGGGGGG	XP_006720324.1:n.*89_*90insGGGGGG
XM_011537185.1:c.*89_*90insGGGGGG	XP_011535487.1:n.*89_*90insGGGGGG
XM_011537186.1:c.*89_*90insGGGGGG	XP_011535488.1:n.*89_*90insGGGGGG
NM_001331238.1:c.*89_*90insGGGGGG	NP_001318167.1:n.*89_*90insGGGGGG
NM_025268.3:c.*89_*90insGGGGGG	NP_079544.1:n.*89_*90insGGGGGG
XM_006720261.3:c.*89_*90insGGGGGG	XP_006720324.1:n.*89_*90insGGGGGG
NM_025268.4:c.*89_*90insGGGGGG MANE Select	NP_079544.1:n.*89_*90insGGGGGG
NM_001331238.2:c.*89_*90insGGGGGG	NP_001318167.1:n.*89_*90insGGGGGG