Canonical Allele Identifier: CA269282651
Gene: SPRED1 HGNC NCBI

Linked Data

dbSNP Id: rs998364290
MyVariant Identifiers: chr15:g.38545316C>G (hg19) chr15:g.38253115C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253115C>G , CM000677.2:g.38253115C>G GRCh38
NC_000015.9:g.38545316C>G , CM000677.1:g.38545316C>G GRCh37
NC_000015.8:g.36332608C>G NCBI36
NG_008980.1:g.5265C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-71C>G MANE Select ENSP00000299084.4:n.-71C>G
ENST00000299084.8:c.-71C>G ENSP00000299084.4:n.-71C>G
ENST00000561205.1:n.268C>G
NM_152594.2:c.-71C>G NP_689807.1:n.-71C>G
XM_005254202.2:c.-71C>G XP_005254259.1:n.-71C>G
XM_005254203.3:c.-118C>G XP_005254260.1:n.-118C>G
XM_005254202.3:c.-71C>G XP_005254259.1:n.-71C>G
XR_001751484.1:n.87+452G>C
NM_152594.3:c.-71C>G MANE Select NP_689807.1:n.-71C>G
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