Canonical Allele Identifier: CA2660178331
Gene: TMEM127 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96255001_96255002insCCGGGTGCACATAGCCC , CM000664.2:g.96255001_96255002insCCGGGTGCACATAGCCC GRCh38
NC_000002.11:g.96920739_96920740insCCGGGTGCACATAGCCC , CM000664.1:g.96920739_96920740insCCGGGTGCACATAGCCC GRCh37
NC_000002.10:g.96284466_96284467insCCGGGTGCACATAGCCC NCBI36
NG_027695.1:g.16012_16013insGGGCTATGTGCACCCGG , LRG_528:g.16012_16013insGGGCTATGTGCACCCGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.245-5_245-4insGGGCTATGTGCACCCGG MANE Select ENSP00000258439.3:n.245-5_245-4insGGGCTATGTGCACCCGG
ENST00000258439.7:c.245-5_245-4insGGGCTATGTGCACCCGG ENSP00000258439.2:n.245-5_245-4insGGGCTATGTGCACCCGG
ENST00000432959.1:c.245-5_245-4insGGGCTATGTGCACCCGG ENSP00000416660.1:n.245-5_245-4insGGGCTATGTGCACCCGG
ENST00000435268.1:c.-8-5_-8-4insGGGCTATGTGCACCCGG ENSP00000411810.1:n.-8-5_-8-4insGGGCTATGTGCACCCGG
NM_001193304.2:c.245-5_245-4insGGGCTATGTGCACCCGG NP_001180233.1:n.245-5_245-4insGGGCTATGTGCACCCGG
NM_017849.3:c.245-5_245-4insGGGCTATGTGCACCCGG , LRG_528t1:c.245-5_245-4insGGGCTATGTGCACCCGG NP_060319.1:n.245-5_245-4insGGGCTATGTGCACCCGG
XM_017004450.1:c.-674-5_-674-4insGGGCTATGTGCACCCGG XP_016859939.1:n.-674-5_-674-4insGGGCTATGTGCACCCGG
XM_017004452.1:c.-8-5_-8-4insGGGCTATGTGCACCCGG XP_016859941.1:n.-8-5_-8-4insGGGCTATGTGCACCCGG
NM_001193304.3:c.245-5_245-4insGGGCTATGTGCACCCGG NP_001180233.1:n.245-5_245-4insGGGCTATGTGCACCCGG
NM_017849.4:c.245-5_245-4insGGGCTATGTGCACCCGG MANE Select NP_060319.1:n.245-5_245-4insGGGCTATGTGCACCCGG