Canonical Allele Identifier: CA1153440202
Gene: C1orf127 HGNC NCBI

Linked Data

dbSNP Id: rs1642976886
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10973158del , CM000663.2:g.10973158del GRCh38
NC_000001.10:g.11033215del , CM000663.1:g.11033215del GRCh37
NC_000001.9:g.10955802del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377004.9:c.127+2998del MANE Select ENSP00000366203.4:n.127+2998del
ENST00000377004.8:c.127+2998del ENSP00000366203.4:n.127+2998del
ENST00000520253.1:c.60+2998del
NM_001170754.1:c.127+2998del NP_001164225.1:n.127+2998del
NM_001170754.2:c.127+2998del MANE Select NP_001164225.1:n.127+2998del
Search 100 bp 5'
Search 100 bp 3'