Canonical Allele Identifier: CA1153439986
Gene: C1orf127 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10972866C= , CM000663.2:g.10972866C= GRCh38
NC_000001.10:g.11032923C= , CM000663.1:g.11032923C= GRCh37
NC_000001.9:g.10955510C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377004.9:c.128-2777G= MANE Select ENSP00000366203.4:n.128-2777G=
ENST00000377004.8:c.128-2777G= ENSP00000366203.4:n.128-2777G=
ENST00000520253.1:c.61-2777G=
NM_001170754.1:c.128-2777G= NP_001164225.1:n.128-2777G=
NM_001170754.2:c.128-2777G= MANE Select NP_001164225.1:n.128-2777G=