Canonical Allele Identifier: CA10762984

Gene: C1orf127

Linked Data

• dbSNP Id: rs12565727
• gnomAD v2: 1-11033082-A-G
• gnomAD v3: 1-10973025-A-G
• gnomAD v4: 1-10973025-A-G
• MyVariant Identifiers: chr1:g.11033082A>G (hg19) ; chr1:g.10973025A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10973025A>G , CM000663.2:g.10973025A>G	GRCh38
NC_000001.10:g.11033082A>G , CM000663.1:g.11033082A>G	GRCh37
NC_000001.9:g.10955669A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000377004.9:c.128-2936T>C MANE Select	ENSP00000366203.4:n.128-2936T>C
ENST00000377004.8:c.128-2936T>C	ENSP00000366203.4:n.128-2936T>C
ENST00000520253.1:c.61-2936T>C
NM_001170754.1:c.128-2936T>C	NP_001164225.1:n.128-2936T>C
NM_001170754.2:c.128-2936T>C MANE Select	NP_001164225.1:n.128-2936T>C