Canonical Allele Identifier: CA1260705321
Gene: SPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891697C= , CM000664.2:g.72891697C= GRCh38
NC_000002.11:g.73118826C= , CM000664.1:g.73118826C= GRCh37
NC_000002.10:g.72972334C= NCBI36
NG_008234.1:g.9315C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*160C= MANE Select ENSP00000234454.5:n.*160C=
ENST00000234454.5:c.*160C= ENSP00000234454.5:n.*160C=
ENST00000498749.1:n.891C=
NM_003124.4:c.*160C= NP_003115.1:n.*160C=
NM_003124.5:c.*160C= MANE Select NP_003115.1:n.*160C=