Canonical Allele Identifier: CA521155586
Gene: C1orf127 HGNC NCBI

Linked Data

dbSNP Id: rs201251174

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10972964_10972965insT , CM000663.2:g.10972964_10972965insT GRCh38
NC_000001.10:g.11033021_11033022insT , CM000663.1:g.11033021_11033022insT GRCh37
NC_000001.9:g.10955608_10955609insT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377004.9:c.128-2876_128-2875insA MANE Select ENSP00000366203.4:n.128-2876_128-2875insA...
ENST00000377004.8:c.128-2876_128-2875insA ENSP00000366203.4:n.128-2876_128-2875insA...
ENST00000520253.1:c.61-2876_61-2875insA
NM_001170754.1:c.128-2876_128-2875insA NP_001164225.1:n.128-2876_128-2875insA
NM_001170754.2:c.128-2876_128-2875insA MANE Select NP_001164225.1:n.128-2876_128-2875insA