Canonical Allele Identifier: CA998565958
Gene: C1orf127 HGNC NCBI

Linked Data

dbSNP Id: rs1642974869

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10972957_10972958insT , CM000663.2:g.10972957_10972958insT GRCh38
NC_000001.10:g.11033014_11033015insT , CM000663.1:g.11033014_11033015insT GRCh37
NC_000001.9:g.10955601_10955602insT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377004.8:n.128-2869_128-2868insA ENSP00000366203.4:n.128-2869_128-2868insA...
ENST00000520253.1:n.61-2869_61-2868insA
NM_001170754.1:n.128-2869_128-2868insA NP_001164225.1:n.128-2869_128-2868insA
NM_001170754.2:c.128-2869_128-2868insA MANE Select NP_001164225.1:n.128-2869_128-2868insA