Canonical Allele Identifier: CA2659569780

Gene: SPR

Linked Data

• gnomAD v4: 2-72891604-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.72891608del , CM000664.2:g.72891608del	GRCh38
NC_000002.11:g.73118737del , CM000664.1:g.73118737del	GRCh37
NC_000002.10:g.72972245del	NCBI36
NG_008234.1:g.9226del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234454.6:c.*71del MANE Select	ENSP00000234454.5:n.*71del
ENST00000234454.5:c.*71del	ENSP00000234454.5:n.*71del
ENST00000498749.1:n.802del
NM_003124.4:c.*71del	NP_003115.1:n.*71del
NM_003124.5:c.*71del MANE Select	NP_003115.1:n.*71del