Canonical Allele Identifier: CA1260705288
Gene: SPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891618C= , CM000664.2:g.72891618C= GRCh38
NC_000002.11:g.73118747C= , CM000664.1:g.73118747C= GRCh37
NC_000002.10:g.72972255C= NCBI36
NG_008234.1:g.9236C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*81C= MANE Select ENSP00000234454.5:n.*81C=
ENST00000234454.5:c.*81C= ENSP00000234454.5:n.*81C=
ENST00000498749.1:n.812C=
NM_003124.4:c.*81C= NP_003115.1:n.*81C=
NM_003124.5:c.*81C= MANE Select NP_003115.1:n.*81C=