Canonical Allele Identifier: CA885376283

Gene: C1orf127

Linked Data

• dbSNP Id: rs1471511917
• gnomAD v3: 1-10972952-A-AT
• gnomAD v4: 1-10972952-A-AT
• MyVariant Identifiers: chr1:g.11033009_11033010insT (hg19) ; chr1:g.10972952_10972953insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10972953dup , CM000663.2:g.10972953dup	GRCh38
NC_000001.10:g.11033010dup , CM000663.1:g.11033010dup	GRCh37
NC_000001.9:g.10955597dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000377004.9:c.128-2864dup MANE Select	ENSP00000366203.4:n.128-2864dup
ENST00000377004.8:c.128-2864dup	ENSP00000366203.4:n.128-2864dup
ENST00000520253.1:c.61-2864dup
NM_001170754.1:c.128-2864dup	NP_001164225.1:n.128-2864dup
NM_001170754.2:c.128-2864dup MANE Select	NP_001164225.1:n.128-2864dup