Canonical Allele Identifier: CA2627714326
Gene: SPRED1 HGNC NCBI

Linked Data

gnomAD v4: 15-38253082-C-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253082C>G , CM000677.2:g.38253082C>G GRCh38
NC_000015.9:g.38545283C>G , CM000677.1:g.38545283C>G GRCh37
NC_000015.8:g.36332575C>G NCBI36
NG_008980.1:g.5232C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-104C>G MANE Select ENSP00000299084.4:n.-104C>G
ENST00000299084.8:c.-104C>G ENSP00000299084.4:n.-104C>G
ENST00000561205.1:n.235C>G
NM_152594.2:c.-104C>G NP_689807.1:n.-104C>G
XM_005254202.2:c.-104C>G XP_005254259.1:n.-104C>G
XM_005254203.3:c.-151C>G XP_005254260.1:n.-151C>G
XM_005254202.3:c.-104C>G XP_005254259.1:n.-104C>G
XR_001751484.1:n.87+485G>C
NM_152594.3:c.-104C>G MANE Select NP_689807.1:n.-104C>G
Search 100 bp 5'
Search 100 bp 3'