Canonical Allele Identifier: CA49798701
Gene: SPR HGNC NCBI

Linked Data

dbSNP Id: rs937577453

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891507_72891508del , CM000664.2:g.72891507_72891508del GRCh38
NC_000002.11:g.73118636_73118637del , CM000664.1:g.73118636_73118637del GRCh37
NC_000002.10:g.72972144_72972145del NCBI36
NG_008234.1:g.9125_9126del

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.756_757del MANE Select ENSP00000234454.5:p.Gly253SerfsTer7
ENST00000234454.5:c.756_757del ENSP00000234454.5:p.Gly253SerfsTer7
ENST00000498749.1:n.701_702del
NM_003124.4:c.756_757del NP_003115.1:p.Gly253SerfsTer7
NM_003124.5:c.756_757del MANE Select NP_003115.1:p.Gly253SerfsTer7