Canonical Allele Identifier: CA2659569880
Gene: SPR HGNC NCBI

Linked Data

gnomAD v4: 2-72891711-T-TA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891712dup , CM000664.2:g.72891712dup GRCh38
NC_000002.11:g.73118841dup , CM000664.1:g.73118841dup GRCh37
NC_000002.10:g.72972349dup NCBI36
NG_008234.1:g.9330dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*175dup MANE Select ENSP00000234454.5:n.*175dup
ENST00000234454.5:c.*175dup ENSP00000234454.5:n.*175dup
ENST00000498749.1:n.906dup
NM_003124.4:c.*175dup NP_003115.1:n.*175dup
NM_003124.5:c.*175dup MANE Select NP_003115.1:n.*175dup
Search 100 bp 5'
Search 100 bp 3'