Canonical Allele Identifier: CA2659569872
Gene: SPR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891701dup , CM000664.2:g.72891701dup GRCh38
NC_000002.11:g.73118830dup , CM000664.1:g.73118830dup GRCh37
NC_000002.10:g.72972338dup NCBI36
NG_008234.1:g.9319dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*164dup MANE Select ENSP00000234454.5:n.*164dup
ENST00000234454.5:c.*164dup ENSP00000234454.5:n.*164dup
ENST00000498749.1:n.895dup
NM_003124.4:c.*164dup NP_003115.1:n.*164dup
NM_003124.5:c.*164dup MANE Select NP_003115.1:n.*164dup