Canonical Allele Identifier: CA521155587
Gene: C1orf127 HGNC NCBI

Linked Data

dbSNP Id: rs1341788513

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10972968del , CM000663.2:g.10972968del GRCh38
NC_000001.10:g.11033025del , CM000663.1:g.11033025del GRCh37
NC_000001.9:g.10955612del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377004.8:n.128-2879del ENSP00000366203.4:n.128-2879del
ENST00000520253.1:n.61-2879del
NM_001170754.1:n.128-2879del NP_001164225.1:n.128-2879del
NM_001170754.2:c.128-2879del MANE Select NP_001164225.1:n.128-2879del