Canonical Allele Identifier: CA269282649

Gene: SPRED1

Linked Data

• dbSNP Id: rs940235924
• MyVariant Identifiers: chr15:g.38545291_38545292insCCCGG (hg19) ; chr15:g.38253090_38253091insCCCGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253093_38253097dup , CM000677.2:g.38253093_38253097dup	GRCh38
NC_000015.9:g.38545294_38545298dup , CM000677.1:g.38545294_38545298dup	GRCh37
NC_000015.8:g.36332586_36332590dup	NCBI36
NG_008980.1:g.5243_5247dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.-93_-89dup MANE Select	ENSP00000299084.4:n.-93_-89dup
ENST00000299084.8:c.-93_-89dup	ENSP00000299084.4:n.-93_-89dup
ENST00000561205.1:n.246_250dup
NM_152594.2:c.-93_-89dup	NP_689807.1:n.-93_-89dup
XM_005254202.2:c.-93_-89dup	XP_005254259.1:n.-93_-89dup
XM_005254203.3:c.-140_-136dup	XP_005254260.1:n.-140_-136dup
XM_005254202.3:c.-93_-89dup	XP_005254259.1:n.-93_-89dup
XR_001751484.1:n.87+472_87+476dup
NM_152594.3:c.-93_-89dup MANE Select	NP_689807.1:n.-93_-89dup