Canonical Allele Identifier: CA998565935
Gene: C1orf127 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10972947T>A , CM000663.2:g.10972947T>A GRCh38
NC_000001.10:g.11033004T>A , CM000663.1:g.11033004T>A GRCh37
NC_000001.9:g.10955591T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377004.8:n.128-2858A>T ENSP00000366203.4:n.128-2858A>T
ENST00000520253.1:n.61-2858A>T
NM_001170754.1:n.128-2858A>T NP_001164225.1:n.128-2858A>T
NM_001170754.2:c.128-2858A>T MANE Select NP_001164225.1:n.128-2858A>T