Canonical Allele Identifier: CA521155579
Gene: C1orf127 HGNC NCBI

Linked Data

dbSNP Id: rs376697353

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10972963_10972964del , CM000663.2:g.10972963_10972964del GRCh38
NC_000001.10:g.11033020_11033021del , CM000663.1:g.11033020_11033021del GRCh37
NC_000001.9:g.10955607_10955608del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377004.8:n.128-2866_128-2865del ENSP00000366203.4:n.128-2866_128-2865del
ENST00000520253.1:n.61-2866_61-2865del
NM_001170754.1:n.128-2866_128-2865del NP_001164225.1:n.128-2866_128-2865del
NM_001170754.2:c.128-2866_128-2865del MANE Select NP_001164225.1:n.128-2866_128-2865del