Canonical Allele Identifier: CA1141326132
Gene: C1orf127 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10972945A= , CM000663.2:g.10972945A= GRCh38
NC_000001.10:g.11033002A= , CM000663.1:g.11033002A= GRCh37
NC_000001.9:g.10955589A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377004.8:n.128-2856T= ENSP00000366203.4:n.128-2856T=
ENST00000520253.1:n.61-2856T=
NM_001170754.1:n.128-2856T= NP_001164225.1:n.128-2856T=
NM_001170754.2:c.128-2856T= MANE Select NP_001164225.1:n.128-2856T=