Canonical Allele Identifier: CA617495220

Gene: SPRED1

Linked Data

• dbSNP Id: rs1566844452
• gnomAD v2: 15-38545454-T-TC
• gnomAD v4: 15-38253253-T-TC
• MyVariant Identifiers: chr15:g.38545454_38545455insC (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253258dup , CM000677.2:g.38253258dup	GRCh38
NC_000015.9:g.38545459dup , CM000677.1:g.38545459dup	GRCh37
NC_000015.8:g.36332751dup	NCBI36
NG_008980.1:g.5408dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.32+41dup MANE Select	ENSP00000299084.4:n.32+41dup
ENST00000299084.8:c.32+41dup	ENSP00000299084.4:n.32+41dup
ENST00000561205.1:n.370+41dup
ENST00000561317.1:c.-96+41dup	ENSP00000453680.1:n.-96+41dup
NM_152594.2:c.32+41dup	NP_689807.1:n.32+41dup
XM_005254202.2:c.32+41dup	XP_005254259.1:n.32+41dup
XM_005254203.3:c.-16+41dup	XP_005254260.1:n.-16+41dup
XM_005254202.3:c.32+41dup	XP_005254259.1:n.32+41dup
XR_001751484.1:n.87+313dup
NM_152594.3:c.32+41dup MANE Select	NP_689807.1:n.32+41dup