Canonical Allele Identifier: CA916198375
Gene: C1orf141 HGNC NCBI

Linked Data

dbSNP Id: rs1558210870

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67135461del , CM000663.2:g.67135461del GRCh38
NC_000001.10:g.67601144del , CM000663.1:g.67601144del GRCh37
NC_000001.9:g.67373732del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371007.6:c.-103-4231del ENSP00000360046.1:n.-103-4231del
ENST00000448166.6:c.-103-4231del ENSP00000415519.2:n.-103-4231del
XM_011541466.1:c.-18+6156del XP_011539768.1:n.-18+6156del
XM_011541466.2:c.-18+6156del XP_011539768.1:n.-18+6156del