Canonical Allele Identifier: CA1260703864

Gene: SPR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.72888411G= , CM000664.2:g.72888411G=	GRCh38
NC_000002.11:g.73115540G= , CM000664.1:g.73115540G=	GRCh37
NC_000002.10:g.72969048G=	NCBI36
NG_008234.1:g.6029G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000234454.6:c.402G= MANE Select	ENSP00000234454.5:p.Leu134=
ENST00000234454.5:c.402G=	ENSP00000234454.5:p.Leu134=
ENST00000498749.1:n.356-9G=
NM_003124.4:c.402G=	NP_003115.1:p.Leu134=
NM_003124.5:c.402G= MANE Select	NP_003115.1:p.Leu134=