Canonical Allele Identifier: CA968819833
Gene: SPRED1 HGNC NCBI

Linked Data

dbSNP Id: rs1888625684
gnomAD v3: 15-38356541-T-G
gnomAD v4: 15-38356541-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38356541T>G , CM000677.2:g.38356541T>G GRCh38
NC_000015.9:g.38648742T>G , CM000677.1:g.38648742T>G GRCh37
NC_000015.8:g.36436034T>G NCBI36
NG_008980.1:g.108691T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.*4877T>G MANE Select ENSP00000299084.4:n.*4877T>G
ENST00000299084.8:c.*4877T>G ENSP00000299084.4:n.*4877T>G
NM_152594.2:c.*4877T>G NP_689807.1:n.*4877T>G
XM_005254202.3:c.*4877T>G XP_005254259.1:n.*4877T>G
XM_011521289.3:c.*4877T>G XP_011519591.1:n.*4877T>G
NM_152594.3:c.*4877T>G MANE Select NP_689807.1:n.*4877T>G
Search 100 bp 5'
Search 100 bp 3'