Canonical Allele Identifier: CA2659569808

Gene: SPR

Linked Data

• gnomAD v4: 2-72891650-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.72891652del , CM000664.2:g.72891652del	GRCh38
NC_000002.11:g.73118781del , CM000664.1:g.73118781del	GRCh37
NC_000002.10:g.72972289del	NCBI36
NG_008234.1:g.9270del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234454.6:c.*115del MANE Select	ENSP00000234454.5:n.*115del
ENST00000234454.5:c.*115del	ENSP00000234454.5:n.*115del
ENST00000498749.1:n.846del
NM_003124.4:c.*115del	NP_003115.1:n.*115del
NM_003124.5:c.*115del MANE Select	NP_003115.1:n.*115del