Canonical Allele Identifier: CA1260705245

Gene: SPR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.72891517G= , CM000664.2:g.72891517G=	GRCh38
NC_000002.11:g.73118646G= , CM000664.1:g.73118646G=	GRCh37
NC_000002.10:g.72972154G=	NCBI36
NG_008234.1:g.9135G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234454.6:c.766G= MANE Select	ENSP00000234454.5:p.Val256=
ENST00000234454.5:c.766G=	ENSP00000234454.5:p.Val256=
ENST00000498749.1:n.711G=
NM_003124.4:c.766G=	NP_003115.1:p.Val256=
NM_003124.5:c.766G= MANE Select	NP_003115.1:p.Val256=