Canonical Allele Identifier: CA2659569832
Gene: SPR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891671del , CM000664.2:g.72891671del GRCh38
NC_000002.11:g.73118800del , CM000664.1:g.73118800del GRCh37
NC_000002.10:g.72972308del NCBI36
NG_008234.1:g.9289del

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*134del MANE Select ENSP00000234454.5:n.*134del
ENST00000234454.5:c.*134del ENSP00000234454.5:n.*134del
ENST00000498749.1:n.865del
NM_003124.4:c.*134del NP_003115.1:n.*134del
NM_003124.5:c.*134del MANE Select NP_003115.1:n.*134del