Canonical Allele Identifier: CA269293955
Gene: SPRED1 HGNC NCBI

Linked Data

dbSNP Id: rs570447852
gnomAD v3: 15-38356538-C-G
gnomAD v4: 15-38356538-C-G
MyVariant Identifiers: chr15:g.38648739C>G (hg19) chr15:g.38356538C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38356538C>G , CM000677.2:g.38356538C>G GRCh38
NC_000015.9:g.38648739C>G , CM000677.1:g.38648739C>G GRCh37
NC_000015.8:g.36436031C>G NCBI36
NG_008980.1:g.108688C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.*4874C>G MANE Select ENSP00000299084.4:n.*4874C>G
ENST00000299084.8:c.*4874C>G ENSP00000299084.4:n.*4874C>G
NM_152594.2:c.*4874C>G NP_689807.1:n.*4874C>G
XM_005254202.3:c.*4874C>G XP_005254259.1:n.*4874C>G
XM_011521289.3:c.*4874C>G XP_011519591.1:n.*4874C>G
NM_152594.3:c.*4874C>G MANE Select NP_689807.1:n.*4874C>G
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