Canonical Allele Identifier: CA7469955
Gene: SPRED1 HGNC NCBI

Linked Data

dbSNP Id: rs183760632
ExAC: 15:38545454 T / A
gnomAD v2: 15-38545454-T-A
gnomAD v3: 15-38253253-T-A
gnomAD v4: 15-38253253-T-A
MyVariant Identifiers: chr15:g.38545454T>A (hg19) chr15:g.38253253T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253253T>A , CM000677.2:g.38253253T>A GRCh38
NC_000015.9:g.38545454T>A , CM000677.1:g.38545454T>A GRCh37
NC_000015.8:g.36332746T>A NCBI36
NG_008980.1:g.5403T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.32+36T>A MANE Select ENSP00000299084.4:n.32+36T>A
ENST00000299084.8:c.32+36T>A ENSP00000299084.4:n.32+36T>A
ENST00000561205.1:n.370+36T>A
ENST00000561317.1:c.-96+36T>A ENSP00000453680.1:n.-96+36T>A
NM_152594.2:c.32+36T>A NP_689807.1:n.32+36T>A
XM_005254202.2:c.32+36T>A XP_005254259.1:n.32+36T>A
XM_005254203.3:c.-16+36T>A XP_005254260.1:n.-16+36T>A
XM_005254202.3:c.32+36T>A XP_005254259.1:n.32+36T>A
XR_001751484.1:n.87+314A>T
NM_152594.3:c.32+36T>A MANE Select NP_689807.1:n.32+36T>A
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