Canonical Allele Identifier: CA1153439975
Gene: C1orf127 HGNC NCBI

Linked Data

dbSNP Id: rs1642973173

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10972830del , CM000663.2:g.10972830del GRCh38
NC_000001.10:g.11032887del , CM000663.1:g.11032887del GRCh37
NC_000001.9:g.10955474del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377004.9:c.128-2741del MANE Select ENSP00000366203.4:n.128-2741del
ENST00000377004.8:c.128-2741del ENSP00000366203.4:n.128-2741del
ENST00000520253.1:c.61-2741del
NM_001170754.1:c.128-2741del NP_001164225.1:n.128-2741del
NM_001170754.2:c.128-2741del MANE Select NP_001164225.1:n.128-2741del