Canonical Allele Identifier: CA1718709289
Gene: CCDC146 HGNC NCBI

Linked Data

dbSNP Id: rs1790815985
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.77133507A>G , CM000669.2:g.77133507A>G GRCh38
NC_000007.13:g.76762824A>G , CM000669.1:g.76762824A>G GRCh37
NC_000007.12:g.76600760A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000285871.5:c.-12+10775A>G MANE Select ENSP00000285871.4:n.-12+10775A>G
ENST00000285871.4:c.-12+10775A>G ENSP00000285871.4:n.-12+10775A>G
ENST00000415750.5:c.-12+11039A>G ENSP00000388649.1:n.-12+11039A>G
NM_020879.2:c.-12+10775A>G NP_065930.2:n.-12+10775A>G
XR_927691.1:n.48-4781T>C
NM_020879.3:c.-12+10775A>G MANE Select NP_065930.2:n.-12+10775A>G
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