Canonical Allele Identifier: CA1153440100
Gene: C1orf127 HGNC NCBI

Linked Data

dbSNP Id: rs72644043

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10972994T>C , CM000663.2:g.10972994T>C GRCh38
NC_000001.10:g.11033051T>C , CM000663.1:g.11033051T>C GRCh37
NC_000001.9:g.10955638T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377004.9:c.128-2905A>G MANE Select ENSP00000366203.4:n.128-2905A>G
ENST00000377004.8:c.128-2905A>G ENSP00000366203.4:n.128-2905A>G
ENST00000520253.1:c.61-2905A>G
NM_001170754.1:c.128-2905A>G NP_001164225.1:n.128-2905A>G
NM_001170754.2:c.128-2905A>G MANE Select NP_001164225.1:n.128-2905A>G