Canonical Allele Identifier: CA1173010182
Gene: C1orf141 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67135433C= , CM000663.2:g.67135433C= GRCh38
NC_000001.10:g.67601116C= , CM000663.1:g.67601116C= GRCh37
NC_000001.9:g.67373704C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371007.6:c.-103-4206G= ENSP00000360046.1:n.-103-4206G=
ENST00000448166.6:c.-103-4206G= ENSP00000415519.2:n.-103-4206G=
XM_011541466.1:c.-18+6181G= XP_011539768.1:n.-18+6181G=
XM_011541466.2:c.-18+6181G= XP_011539768.1:n.-18+6181G=