Canonical Allele Identifier: CA2577002023

Gene: SPR

Linked Data

• gnomAD v4: 2-72891544-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.72891549del , CM000664.2:g.72891549del	GRCh38
NC_000002.11:g.73118678del , CM000664.1:g.73118678del	GRCh37
NC_000002.10:g.72972186del	NCBI36
NG_008234.1:g.9167del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234454.6:c.*12del MANE Select	ENSP00000234454.5:n.*12del
ENST00000234454.5:c.*12del	ENSP00000234454.5:n.*12del
ENST00000498749.1:n.743del
NM_003124.4:c.*12del	NP_003115.1:n.*12del
NM_003124.5:c.*12del MANE Select	NP_003115.1:n.*12del