Canonical Allele Identifier: CA2170765569
Gene: SPRED1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38252993C= , CM000677.2:g.38252993C= GRCh38
NC_000015.9:g.38545194C= , CM000677.1:g.38545194C= GRCh37
NC_000015.8:g.36332486C= NCBI36
NG_008980.1:g.5143C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-193C= MANE Select ENSP00000299084.4:n.-193C=
ENST00000299084.8:c.-193C= ENSP00000299084.4:n.-193C=
ENST00000561205.1:n.146C=
NM_152594.2:c.-193C= NP_689807.1:n.-193C=
XM_005254202.2:c.-193C= XP_005254259.1:n.-193C=
XM_005254203.3:c.-240C= XP_005254260.1:n.-240C=
XM_005254202.3:c.-193C= XP_005254259.1:n.-193C=
XR_001751484.1:n.87+574G=
NM_152594.3:c.-193C= MANE Select NP_689807.1:n.-193C=
Search 100 bp 5'
Search 100 bp 3'