Canonical Allele Identifier: CA269282650
Gene: SPRED1 HGNC NCBI

Linked Data

dbSNP Id: rs1046813969
gnomAD v2: 15-38545314-C-T
gnomAD v3: 15-38253113-C-T
gnomAD v4: 15-38253113-C-T
MyVariant Identifiers: chr15:g.38545314C>T (hg19) chr15:g.38253113C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253113C>T , CM000677.2:g.38253113C>T GRCh38
NC_000015.9:g.38545314C>T , CM000677.1:g.38545314C>T GRCh37
NC_000015.8:g.36332606C>T NCBI36
NG_008980.1:g.5263C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-73C>T MANE Select ENSP00000299084.4:n.-73C>T
ENST00000299084.8:c.-73C>T ENSP00000299084.4:n.-73C>T
ENST00000561205.1:n.266C>T
NM_152594.2:c.-73C>T NP_689807.1:n.-73C>T
XM_005254202.2:c.-73C>T XP_005254259.1:n.-73C>T
XM_005254203.3:c.-120C>T XP_005254260.1:n.-120C>T
XM_005254202.3:c.-73C>T XP_005254259.1:n.-73C>T
XR_001751484.1:n.87+454G>A
NM_152594.3:c.-73C>T MANE Select NP_689807.1:n.-73C>T
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