Canonical Allele Identifier: CA2750449386
Gene: SPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891642_72891643insACAACCCCAAACACACCCAACA , CM000664.2:g.72891642_72891643insACAACCCCAAACACACCCAACA GRCh38
NC_000002.11:g.73118771_73118772insACAACCCCAAACACACCCAACA , CM000664.1:g.73118771_73118772insACAACCCCAAACACACCCAACA GRCh37
NC_000002.10:g.72972279_72972280insACAACCCCAAACACACCCAACA NCBI36
NG_008234.1:g.9260_9261insACAACCCCAAACACACCCAACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*105_*106insACAACCCCAAACACACCCAACA MANE Select ENSP00000234454.5:n.*105_*106insACAACCCCAAACACACCCAACA
ENST00000234454.5:c.*105_*106insACAACCCCAAACACACCCAACA ENSP00000234454.5:n.*105_*106insACAACCCCAAACACACCCAACA
ENST00000498749.1:n.836_837insACAACCCCAAACACACCCAACA
NM_003124.4:c.*105_*106insACAACCCCAAACACACCCAACA NP_003115.1:n.*105_*106insACAACCCCAAACACACCCAACA
NM_003124.5:c.*105_*106insACAACCCCAAACACACCCAACA MANE Select NP_003115.1:n.*105_*106insACAACCCCAAACACACCCAACA