Canonical Allele Identifier: CA1141487838
Gene: C1orf141 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67135391A= , CM000663.2:g.67135391A= GRCh38
NC_000001.10:g.67601074A= , CM000663.1:g.67601074A= GRCh37
NC_000001.9:g.67373662A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371007.6:c.-103-4164T= ENSP00000360046.1:n.-103-4164T=
ENST00000448166.6:c.-103-4164T= ENSP00000415519.2:n.-103-4164T=
XM_011541466.1:c.-18+6223T= XP_011539768.1:n.-18+6223T=
XM_011541466.2:c.-18+6223T= XP_011539768.1:n.-18+6223T=
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