Canonical Allele Identifier: CA2577002026
Gene: SPR HGNC NCBI

Linked Data

gnomAD v4: 2-72891607-CCA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891611_72891612del , CM000664.2:g.72891611_72891612del GRCh38
NC_000002.11:g.73118740_73118741del , CM000664.1:g.73118740_73118741del GRCh37
NC_000002.10:g.72972248_72972249del NCBI36
NG_008234.1:g.9229_9230del

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*74_*75del MANE Select ENSP00000234454.5:n.*74_*75del
ENST00000234454.5:c.*74_*75del ENSP00000234454.5:n.*74_*75del
ENST00000498749.1:n.805_806del
NM_003124.4:c.*74_*75del NP_003115.1:n.*74_*75del
NM_003124.5:c.*74_*75del MANE Select NP_003115.1:n.*74_*75del
Search 100 bp 5'
Search 100 bp 3'