Canonical Allele Identifier: CA998565974
Gene: C1orf127 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10972968T>G , CM000663.2:g.10972968T>G GRCh38
NC_000001.10:g.11033025T>G , CM000663.1:g.11033025T>G GRCh37
NC_000001.9:g.10955612T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377004.8:n.128-2879A>C ENSP00000366203.4:n.128-2879A>C
ENST00000520253.1:n.61-2879A>C
NM_001170754.1:n.128-2879A>C NP_001164225.1:n.128-2879A>C
NM_001170754.2:c.128-2879A>C MANE Select NP_001164225.1:n.128-2879A>C