Canonical Allele Identifier: CA2170765728
Gene: SPRED1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253134C= , CM000677.2:g.38253134C= GRCh38
NC_000015.9:g.38545335C= , CM000677.1:g.38545335C= GRCh37
NC_000015.8:g.36332627C= NCBI36
NG_008980.1:g.5284C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-52C= MANE Select ENSP00000299084.4:n.-52C=
ENST00000299084.8:c.-52C= ENSP00000299084.4:n.-52C=
ENST00000561205.1:n.287C=
NM_152594.2:c.-52C= NP_689807.1:n.-52C=
XM_005254202.2:c.-52C= XP_005254259.1:n.-52C=
XM_005254203.3:c.-99C= XP_005254260.1:n.-99C=
XM_005254202.3:c.-52C= XP_005254259.1:n.-52C=
XR_001751484.1:n.87+433G=
NM_152594.3:c.-52C= MANE Select NP_689807.1:n.-52C=
Search 100 bp 5'
Search 100 bp 3'