Canonical Allele Identifier: CA1260705294
Gene: SPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891637T= , CM000664.2:g.72891637T= GRCh38
NC_000002.11:g.73118766T= , CM000664.1:g.73118766T= GRCh37
NC_000002.10:g.72972274T= NCBI36
NG_008234.1:g.9255T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*100T= MANE Select ENSP00000234454.5:n.*100T=
ENST00000234454.5:c.*100T= ENSP00000234454.5:n.*100T=
ENST00000498749.1:n.831T=
NM_003124.4:c.*100T= NP_003115.1:n.*100T=
NM_003124.5:c.*100T= MANE Select NP_003115.1:n.*100T=