Canonical Allele Identifier: CA17879750

Gene: C1orf127

Linked Data

• dbSNP Id: rs953211606
• MyVariant Identifiers: chr1:g.11032777T>A (hg19) ; chr1:g.10972720T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10972720T>A , CM000663.2:g.10972720T>A	GRCh38
NC_000001.10:g.11032777T>A , CM000663.1:g.11032777T>A	GRCh37
NC_000001.9:g.10955364T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377004.9:c.128-2631A>T MANE Select	ENSP00000366203.4:n.128-2631A>T
ENST00000377004.8:c.128-2631A>T	ENSP00000366203.4:n.128-2631A>T
ENST00000520253.1:c.61-2631A>T
NM_001170754.1:c.128-2631A>T	NP_001164225.1:n.128-2631A>T
NM_001170754.2:c.128-2631A>T MANE Select	NP_001164225.1:n.128-2631A>T