Canonical Allele Identifier: CA1260705297
Gene: SPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891642A= , CM000664.2:g.72891642A= GRCh38
NC_000002.11:g.73118771A= , CM000664.1:g.73118771A= GRCh37
NC_000002.10:g.72972279A= NCBI36
NG_008234.1:g.9260A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*105A= MANE Select ENSP00000234454.5:n.*105A=
ENST00000234454.5:c.*105A= ENSP00000234454.5:n.*105A=
ENST00000498749.1:n.836A=
NM_003124.4:c.*105A= NP_003115.1:n.*105A=
NM_003124.5:c.*105A= MANE Select NP_003115.1:n.*105A=