Canonical Allele Identifier: CA521155585

Gene: C1orf127

Linked Data

• gnomAD v2: 1:11033013 A / T
• MyVariant Identifiers: chr1:g.11033013A>T (hg19) ; chr1:g.10972956A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10972956A>T , CM000663.2:g.10972956A>T	GRCh38
NC_000001.10:g.11033013A>T , CM000663.1:g.11033013A>T	GRCh37
NC_000001.9:g.10955600A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000377004.8:c.128-2867T>A	ENSP00000366203.4:n.128-2867T>A
ENST00000520253.1:c.61-2867T>A
NM_001170754.1:c.128-2867T>A	NP_001164225.1:n.128-2867T>A
NM_001170754.2:c.128-2867T>A MANE Select	NP_001164225.1:n.128-2867T>A