Canonical Allele Identifier: CA2659569828
Gene: SPR HGNC NCBI

Linked Data

gnomAD v4: 2-72891664-C-CAGG
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891664_72891665insAGG , CM000664.2:g.72891664_72891665insAGG GRCh38
NC_000002.11:g.73118793_73118794insAGG , CM000664.1:g.73118793_73118794insAGG GRCh37
NC_000002.10:g.72972301_72972302insAGG NCBI36
NG_008234.1:g.9282_9283insAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*127_*128insAGG MANE Select ENSP00000234454.5:n.*127_*128insAGG
ENST00000234454.5:c.*127_*128insAGG ENSP00000234454.5:n.*127_*128insAGG
ENST00000498749.1:n.858_859insAGG
NM_003124.4:c.*127_*128insAGG NP_003115.1:n.*127_*128insAGG
NM_003124.5:c.*127_*128insAGG MANE Select NP_003115.1:n.*127_*128insAGG
Search 100 bp 5'
Search 100 bp 3'