Canonical Allele Identifier: CA1173010280
Gene: C1orf141 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67135528T= , CM000663.2:g.67135528T= GRCh38
NC_000001.10:g.67601211T= , CM000663.1:g.67601211T= GRCh37
NC_000001.9:g.67373799T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371007.6:c.-103-4301A= ENSP00000360046.1:n.-103-4301A=
ENST00000448166.6:c.-103-4301A= ENSP00000415519.2:n.-103-4301A=
XM_011541466.1:c.-18+6086A= XP_011539768.1:n.-18+6086A=
XM_011541466.2:c.-18+6086A= XP_011539768.1:n.-18+6086A=