Canonical Allele Identifier: CA17879865

Gene: C1orf127

Linked Data

• dbSNP Id: rs376697353
• gnomAD v2: 1-11033010-T-TA
• gnomAD v3: 1-10972953-T-TA
• gnomAD v4: 1-10972953-T-TA
• MyVariant Identifiers: chr1:g.11033012_11033013insA (hg19) ; chr1:g.11033010_11033011insA (hg19) ; chr1:g.10972955_10972956insA (hg38) ; chr1:g.10972953_10972954insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10972964dup , CM000663.2:g.10972964dup	GRCh38
NC_000001.10:g.11033021dup , CM000663.1:g.11033021dup	GRCh37
NC_000001.9:g.10955608dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000377004.9:c.128-2865dup MANE Select	ENSP00000366203.4:n.128-2865dup
ENST00000377004.8:c.128-2865dup	ENSP00000366203.4:n.128-2865dup
ENST00000520253.1:c.61-2865dup
NM_001170754.1:c.128-2865dup	NP_001164225.1:n.128-2865dup
NM_001170754.2:c.128-2865dup MANE Select	NP_001164225.1:n.128-2865dup