Canonical Allele Identifier: CA1260705300
Gene: SPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891648G= , CM000664.2:g.72891648G= GRCh38
NC_000002.11:g.73118777G= , CM000664.1:g.73118777G= GRCh37
NC_000002.10:g.72972285G= NCBI36
NG_008234.1:g.9266G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*111G= MANE Select ENSP00000234454.5:n.*111G=
ENST00000234454.5:c.*111G= ENSP00000234454.5:n.*111G=
ENST00000498749.1:n.842G=
NM_003124.4:c.*111G= NP_003115.1:n.*111G=
NM_003124.5:c.*111G= MANE Select NP_003115.1:n.*111G=