Canonical Allele Identifier: CA2170765853
Gene: SPRED1 HGNC NCBI

Linked Data

dbSNP Id: rs1894018764
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253217_38253218insTAATA , CM000677.2:g.38253217_38253218insTAATA GRCh38
NC_000015.9:g.38545418_38545419insTAATA , CM000677.1:g.38545418_38545419insTAATA GRCh37
NC_000015.8:g.36332710_36332711insTAATA NCBI36
NG_008980.1:g.5367_5368insTAATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.32_32+1insTAATA MANE Select ENSP00000299084.4:p.Ser13IlefsTer11
ENST00000299084.8:c.32_32+1insTAATA ENSP00000299084.4:p.Ser13IlefsTer11
ENST00000561205.1:n.370_370+1insTAATA
ENST00000561317.1:c.-96_-96+1insTAATA ENSP00000453680.1:n.-96_-96+1insTAATA
NM_152594.2:c.32_32+1insTAATA NP_689807.1:p.Ser13IlefsTer11
XM_005254202.2:c.32_32+1insTAATA XP_005254259.1:p.Glu11AspfsTer25
XM_005254203.3:c.-16_-16+1insTAATA XP_005254260.1:n.-16_-16+1insTAATA
XM_005254202.3:c.32_32+1insTAATA XP_005254259.1:p.Glu11AspfsTer25
XR_001751484.1:n.87+350_87+351insATTAT
NM_152594.3:c.32_32+1insTAATA MANE Select NP_689807.1:p.Ser13IlefsTer11
Search 100 bp 5'
Search 100 bp 3'