Canonical Allele Identifier: CA2699654473

Gene: SPR

Linked Data

• dbSNP Id: rs2105243452

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.72891579T>C , CM000664.2:g.72891579T>C	GRCh38
NC_000002.11:g.73118708T>C , CM000664.1:g.73118708T>C	GRCh37
NC_000002.10:g.72972216T>C	NCBI36
NG_008234.1:g.9197T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234454.6:c.*42T>C MANE Select	ENSP00000234454.5:n.*42T>C
ENST00000234454.5:c.*42T>C	ENSP00000234454.5:n.*42T>C
ENST00000498749.1:n.773T>C
NM_003124.4:c.*42T>C	NP_003115.1:n.*42T>C
NM_003124.5:c.*42T>C MANE Select	NP_003115.1:n.*42T>C