Canonical Allele Identifier: CA1260705198
Gene: SPR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891393G= , CM000664.2:g.72891393G= GRCh38
NC_000002.11:g.73118522G= , CM000664.1:g.73118522G= GRCh37
NC_000002.10:g.72972030G= NCBI36
NG_008234.1:g.9011G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.642G= MANE Select ENSP00000234454.5:p.Val214=
ENST00000234454.5:c.642G= ENSP00000234454.5:p.Val214=
ENST00000498749.1:n.587G=
NM_003124.4:c.642G= NP_003115.1:p.Val214=
NM_003124.5:c.642G= MANE Select NP_003115.1:p.Val214=
Search 100 bp 5'
Search 100 bp 3'