Canonical Allele Identifier: CA1260705267
Gene: SPR HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891573C= , CM000664.2:g.72891573C= GRCh38
NC_000002.11:g.73118702C= , CM000664.1:g.73118702C= GRCh37
NC_000002.10:g.72972210C= NCBI36
NG_008234.1:g.9191C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*36C= MANE Select ENSP00000234454.5:n.*36C=
ENST00000234454.5:c.*36C= ENSP00000234454.5:n.*36C=
ENST00000498749.1:n.767C=
NM_003124.4:c.*36C= NP_003115.1:n.*36C=
NM_003124.5:c.*36C= MANE Select NP_003115.1:n.*36C=
Search 100 bp 5'
Search 100 bp 3'