Canonical Allele Identifier: CA2006885
Gene: CCDC141 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs17362588

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178856319G>A , CM000664.2:g.178856319G>A GRCh38
NC_000002.10:g.179429291G>A NCBI36
NC_000002.11:g.179721046G>A , CM000664.1:g.179721046G>A GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000343876.6:n.1135C>T ENSP00000344627.2:p.Arg379Trp
ENST00000420890.6:c.2803C>T ENSP00000395995.2:p.Arg935Trp
ENST00000443758.5:c.2803C>T ENSP00000390190.1:p.Arg935Trp
NM_173648.3:c.2803C>T VV NP_775919.3:p.Arg935Trp
XM_011510991.1:c.2803C>T XP_011509293.1:p.Arg935Trp
XM_011510992.1:c.2803C>T XP_011509294.1:p.Arg935Trp
XM_011510993.1:c.2623C>T XP_011509295.1:p.Arg875Trp
XM_011510994.1:c.859C>T XP_011509296.1:p.Arg287Trp
XR_923628.1:n.1352+27665G>A