Canonical Allele Identifier: CA391931848
Gene: SPRED1 HGNC NCBI

Linked Data

gnomAD v4: 15-38253212-C-G
MyVariant Identifiers: chr15:g.38545413C>G (hg19) chr15:g.38253212C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253212C>G , CM000677.2:g.38253212C>G GRCh38
NC_000015.9:g.38545413C>G , CM000677.1:g.38545413C>G GRCh37
NC_000015.8:g.36332705C>G NCBI36
NG_008980.1:g.5362C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.27C>G MANE Select ENSP00000299084.4:p.Asp9Glu
ENST00000299084.8:c.27C>G ENSP00000299084.4:p.Asp9Glu
ENST00000561205.1:n.365C>G
ENST00000561317.1:c.-101C>G ENSP00000453680.1:n.-101C>G
NM_152594.2:c.27C>G NP_689807.1:p.Asp9Glu
XM_005254202.2:c.27C>G XP_005254259.1:p.Asp9Glu
XM_005254203.3:c.-21C>G XP_005254260.1:n.-21C>G
XM_005254202.3:c.27C>G XP_005254259.1:p.Asp9Glu
XR_001751484.1:n.87+355G>C
NM_152594.3:c.27C>G MANE Select NP_689807.1:p.Asp9Glu
Search 100 bp 5'
Search 100 bp 3'