Canonical Allele Identifier: CA712588214
Gene: SPRED1 HGNC NCBI

Linked Data

dbSNP Id: rs531519324
gnomAD v3: 15-38253023-T-TG
gnomAD v4: 15-38253023-T-TG
MyVariant Identifiers: chr15:g.38545224_38545225insG (hg19) chr15:g.38253023_38253024insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253030dup , CM000677.2:g.38253030dup GRCh38
NC_000015.9:g.38545231dup , CM000677.1:g.38545231dup GRCh37
NC_000015.8:g.36332523dup NCBI36
NG_008980.1:g.5180dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-156dup MANE Select ENSP00000299084.4:n.-156dup
ENST00000299084.8:c.-156dup ENSP00000299084.4:n.-156dup
ENST00000561205.1:n.183dup
NM_152594.2:c.-156dup NP_689807.1:n.-156dup
XM_005254202.2:c.-156dup XP_005254259.1:n.-156dup
XM_005254203.3:c.-203dup XP_005254260.1:n.-203dup
XM_005254202.3:c.-156dup XP_005254259.1:n.-156dup
XR_001751484.1:n.87+543dup
NM_152594.3:c.-156dup MANE Select NP_689807.1:n.-156dup
Search 100 bp 5'
Search 100 bp 3'