Canonical Allele Identifier: CA842429935
Gene: CCDC146 HGNC NCBI

Linked Data

dbSNP Id: rs1198281023
MyVariant Identifiers: chr7:g.76762786T>A (hg19) chr7:g.77133469T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.77133469T>A , CM000669.2:g.77133469T>A GRCh38
NC_000007.13:g.76762786T>A , CM000669.1:g.76762786T>A GRCh37
NC_000007.12:g.76600722T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000285871.5:c.-12+10737T>A MANE Select ENSP00000285871.4:n.-12+10737T>A
ENST00000285871.4:c.-12+10737T>A ENSP00000285871.4:n.-12+10737T>A
ENST00000415750.5:c.-12+11001T>A ENSP00000388649.1:n.-12+11001T>A
NM_020879.2:c.-12+10737T>A NP_065930.2:n.-12+10737T>A
XR_927691.1:n.48-4743A>T
NM_020879.3:c.-12+10737T>A MANE Select NP_065930.2:n.-12+10737T>A
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