Canonical Allele Identifier: CA2573135942
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 1349666
ClinVar RCV Id: RCV002047095
dbSNP Id: rs2104283392

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96253903_96254383del , CM000664.2:g.96253903_96254383del GRCh38
NC_000002.11:g.96919641_96920121del , CM000664.1:g.96919641_96920121del GRCh37
NC_000002.10:g.96283368_96283848del NCBI36
NG_027695.1:g.16634_17114del , LRG_528:g.16634_17114del

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.410-265_625del
ENST00000258439.7:c.410-265_625del
ENST00000432959.1:c.410-265_625del
ENST00000435268.1:c.158-265_373del
NM_001193304.2:c.410-265_625del
NM_017849.3:c.410-265_625del , LRG_528t1:c.410-265_625del
XM_017004450.1:c.-509-265_-294del
XM_017004452.1:c.158-265_373del
NM_001193304.3:c.410-265_625del
NM_017849.4:c.410-265_625del