Canonical Allele Identifier: CA1260705310
Gene: SPR HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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