Canonical Allele Identifier: CA3254829
Gene: CCDC152 HGNC NCBI
SELENOP HGNC NCBI
MyVariant.info:
GRCh38 chr5:g.42800706C>T
GRCh37 chr5:g.42800808C>T
gnomAD v2:
5:42800808 C / T
gnomAD v3:
5:42800706 C / T
gnomAD v4:
chr5-42800706-C-T
Joint Max Group AF 0.4469343 (AMR)
Genomes Max Group AF 0.37172721 (AMR)
Exomes Max Group AF 0.47276048 (AMR)
dbSNP:
7579
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.42800706C>T , CM000667.2:g.42800706C>T GRCh38
NC_000005.9:g.42800808C>T , CM000667.1:g.42800808C>T GRCh37
NC_000005.8:g.42836565C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361970.10:c.*925C>T (CCDC152) MANE Select ENSP00000354888.5:n.*925C>T
ENST00000514985.6:c.*14G>A (SELENOP) MANE Select ENSP00000420939.1:n.*14G>A
ENST00000361970.9:c.*925C>T (CCDC152) ENSP00000354888.5:n.*925C>T
ENST00000506577.5:c.*14G>A (SELENOP) ENSP00000425915.1:n.*14G>A
ENST00000511224.5:c.*14G>A (SELENOP) ENSP00000427671.1:n.*14G>A
ENST00000512980.5:n.3352G>A (SELENOP)
ENST00000514985.5:c.*14G>A (SELENOP) ENSP00000420939.1:n.*14G>A
NM_001085486.1:c.*14G>A (SELENOP) NP_001078955.1:n.*14G>A
NM_001093726.1:c.*14G>A (SELENOP) NP_001087195.1:n.*14G>A
NM_001134848.1:c.*925C>T (CCDC152) NP_001128320.1:n.*925C>T
NM_005410.2:c.*14G>A (SELENOP) NP_005401.3:n.*14G>A
NM_001085486.2:c.*14G>A (SELENOP) NP_001078955.1:n.*14G>A
NM_001093726.2:c.*14G>A (SELENOP) NP_001087195.1:n.*14G>A
NM_005410.3:c.*14G>A (SELENOP) NP_005401.3:n.*14G>A
NM_001134848.2:c.*925C>T (CCDC152) MANE Select NP_001128320.1:n.*925C>T
NM_005410.4:c.*14G>A (SELENOP) MANE Select NP_005401.3:n.*14G>A
NM_001085486.3:c.*14G>A (SELENOP) NP_001078955.1:n.*14G>A
NM_001093726.3:c.*14G>A (SELENOP) NP_001087195.1:n.*14G>A
Search 100 bp 5'
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