Canonical Allele Identifier: CA998565892
Gene: C1orf127 HGNC NCBI

Linked Data

gnomAD v3: 1-10972882-T-G
gnomAD v4: 1-10972882-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10972882T>G , CM000663.2:g.10972882T>G GRCh38
NC_000001.10:g.11032939T>G , CM000663.1:g.11032939T>G GRCh37
NC_000001.9:g.10955526T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377004.9:c.128-2793A>C MANE Select ENSP00000366203.4:n.128-2793A>C
ENST00000377004.8:c.128-2793A>C ENSP00000366203.4:n.128-2793A>C
ENST00000520253.1:c.61-2793A>C
NM_001170754.1:c.128-2793A>C NP_001164225.1:n.128-2793A>C
NM_001170754.2:c.128-2793A>C MANE Select NP_001164225.1:n.128-2793A>C