Canonical Allele Identifier: CA1153439933
Gene: C1orf127 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10972764C= , CM000663.2:g.10972764C= GRCh38
NC_000001.10:g.11032821C= , CM000663.1:g.11032821C= GRCh37
NC_000001.9:g.10955408C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377004.9:c.128-2675G= MANE Select ENSP00000366203.4:n.128-2675G=
ENST00000377004.8:c.128-2675G= ENSP00000366203.4:n.128-2675G=
ENST00000520253.1:c.61-2675G=
NM_001170754.1:c.128-2675G= NP_001164225.1:n.128-2675G=
NM_001170754.2:c.128-2675G= MANE Select NP_001164225.1:n.128-2675G=
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