Canonical Allele Identifier: CA7469959
Gene: SPRED1 HGNC NCBI

Linked Data

dbSNP Id: rs189604029
ExAC: 15:38545461 A / G
gnomAD v2: 15-38545461-A-G
gnomAD v3: 15-38253260-A-G
gnomAD v4: 15-38253260-A-G
MyVariant Identifiers: chr15:g.38545461A>G (hg19) chr15:g.38253260A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253260A>G , CM000677.2:g.38253260A>G GRCh38
NC_000015.9:g.38545461A>G , CM000677.1:g.38545461A>G GRCh37
NC_000015.8:g.36332753A>G NCBI36
NG_008980.1:g.5410A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.32+43A>G MANE Select ENSP00000299084.4:n.32+43A>G
ENST00000299084.8:c.32+43A>G ENSP00000299084.4:n.32+43A>G
ENST00000561205.1:n.370+43A>G
ENST00000561317.1:c.-96+43A>G ENSP00000453680.1:n.-96+43A>G
NM_152594.2:c.32+43A>G NP_689807.1:n.32+43A>G
XM_005254202.2:c.32+43A>G XP_005254259.1:n.32+43A>G
XM_005254203.3:c.-16+43A>G XP_005254260.1:n.-16+43A>G
XM_005254202.3:c.32+43A>G XP_005254259.1:n.32+43A>G
XR_001751484.1:n.87+307T>C
NM_152594.3:c.32+43A>G MANE Select NP_689807.1:n.32+43A>G
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