Canonical Allele Identifier: CA521155585
Gene: C1orf127 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10972956A>T , CM000663.2:g.10972956A>T GRCh38
NC_000001.10:g.11033013A>T , CM000663.1:g.11033013A>T GRCh37
NC_000001.9:g.10955600A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377004.8:n.128-2867T>A ENSP00000366203.4:n.128-2867T>A
ENST00000520253.1:n.61-2867T>A
NM_001170754.1:n.128-2867T>A NP_001164225.1:n.128-2867T>A
NM_001170754.2:c.128-2867T>A MANE Select NP_001164225.1:n.128-2867T>A