Canonical Allele Identifier: CA2660175538

Gene: TMEM127

Linked Data

• gnomAD v4: 2-96251909-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96251911del , CM000664.2:g.96251911del	GRCh38
NC_000002.11:g.96917649del , CM000664.1:g.96917649del	GRCh37
NC_000002.10:g.96281376del	NCBI36
NG_027695.1:g.19104del , LRG_528:g.19104del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.*1898del MANE Select	ENSP00000258439.3:n.*1898del
ENST00000258439.7:c.*1898del	ENSP00000258439.2:n.*1898del
ENST00000432959.1:c.*1898del	ENSP00000416660.1:n.*1898del
NM_001193304.2:c.*1898del	NP_001180233.1:n.*1898del
NM_017849.3:c.*1898del , LRG_528t1:c.*1898del	NP_060319.1:n.*1898del
XM_017004450.1:c.*1199del	XP_016859939.1:n.*1199del
XM_017004452.1:c.*1898del	XP_016859941.1:n.*1898del
NM_001193304.3:c.*1898del	NP_001180233.1:n.*1898del
NM_017849.4:c.*1898del MANE Select	NP_060319.1:n.*1898del