Canonical Allele Identifier: CA1173013978
Gene: C1orf141 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67135206A= , CM000663.2:g.67135206A= GRCh38
NC_000001.10:g.67600889A= , CM000663.1:g.67600889A= GRCh37
NC_000001.9:g.67373477A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371007.6:c.-103-3979T= ENSP00000360046.1:n.-103-3979T=
ENST00000448166.6:c.-103-3979T= ENSP00000415519.2:n.-103-3979T=
XM_011541466.1:c.-18+6408T= XP_011539768.1:n.-18+6408T=
XM_011541466.2:c.-18+6408T= XP_011539768.1:n.-18+6408T=