Canonical Allele Identifier: CA2659569838

Gene: SPR

Linked Data

• gnomAD v4: 2-72891671-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.72891672dup , CM000664.2:g.72891672dup	GRCh38
NC_000002.11:g.73118801dup , CM000664.1:g.73118801dup	GRCh37
NC_000002.10:g.72972309dup	NCBI36
NG_008234.1:g.9290dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234454.6:c.*135dup MANE Select	ENSP00000234454.5:n.*135dup
ENST00000234454.5:c.*135dup	ENSP00000234454.5:n.*135dup
ENST00000498749.1:n.866dup
NM_003124.4:c.*135dup	NP_003115.1:n.*135dup
NM_003124.5:c.*135dup MANE Select	NP_003115.1:n.*135dup