Canonical Allele Identifier: CA2660175813

Gene: TMEM127

Linked Data

• gnomAD v4: 2-96252412-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96252415del , CM000664.2:g.96252415del	GRCh38
NC_000002.11:g.96918153del , CM000664.1:g.96918153del	GRCh37
NC_000002.10:g.96281880del	NCBI36
NG_027695.1:g.18601del , LRG_528:g.18601del

Transcript Alleles

HGVS	Amino-acid change
ENST00000258439.8:c.*1395del MANE Select	ENSP00000258439.3:n.*1395del
ENST00000258439.7:c.*1395del	ENSP00000258439.2:n.*1395del
ENST00000432959.1:c.*1395del	ENSP00000416660.1:n.*1395del
NM_001193304.2:c.*1395del	NP_001180233.1:n.*1395del
NM_017849.3:c.*1395del , LRG_528t1:c.*1395del	NP_060319.1:n.*1395del
XM_017004450.1:c.*696del	XP_016859939.1:n.*696del
XM_017004452.1:c.*1395del	XP_016859941.1:n.*1395del
NM_001193304.3:c.*1395del	NP_001180233.1:n.*1395del
NM_017849.4:c.*1395del MANE Select	NP_060319.1:n.*1395del