Canonical Allele Identifier: CA269293952
Gene: SPRED1 HGNC NCBI

Linked Data

dbSNP Id: rs527516741
gnomAD v3: 15-38356501-A-T
gnomAD v4: 15-38356501-A-T
MyVariant Identifiers: chr15:g.38648702A>T (hg19) chr15:g.38356501A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38356501A>T , CM000677.2:g.38356501A>T GRCh38
NC_000015.9:g.38648702A>T , CM000677.1:g.38648702A>T GRCh37
NC_000015.8:g.36435994A>T NCBI36
NG_008980.1:g.108651A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.*4837A>T MANE Select ENSP00000299084.4:n.*4837A>T
ENST00000299084.8:c.*4837A>T ENSP00000299084.4:n.*4837A>T
NM_152594.2:c.*4837A>T NP_689807.1:n.*4837A>T
XM_005254202.3:c.*4837A>T XP_005254259.1:n.*4837A>T
XM_011521289.3:c.*4837A>T XP_011519591.1:n.*4837A>T
NM_152594.3:c.*4837A>T MANE Select NP_689807.1:n.*4837A>T
Search 100 bp 5'
Search 100 bp 3'