Canonical Allele Identifier: CA269293942

Gene: SPRED1

Linked Data

• dbSNP Id: rs946356477
• gnomAD v2: 15-38648587-A-AT
• gnomAD v3: 15-38356386-A-AT
• gnomAD v4: 15-38356386-A-AT
• MyVariant Identifiers: chr15:g.38648587_38648588insT (hg19) ; chr15:g.38356386_38356387insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38356387dup , CM000677.2:g.38356387dup	GRCh38
NC_000015.9:g.38648588dup , CM000677.1:g.38648588dup	GRCh37
NC_000015.8:g.36435880dup	NCBI36
NG_008980.1:g.108537dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.*4723dup MANE Select	ENSP00000299084.4:n.*4723dup
ENST00000299084.8:c.*4723dup	ENSP00000299084.4:n.*4723dup
NM_152594.2:c.*4723dup	NP_689807.1:n.*4723dup
XM_005254202.2:c.*4723dup	XP_005254259.1:n.*4723dup
XM_005254203.3:c.*4723dup	XP_005254260.1:n.*4723dup
XM_011521288.1:c.*4723dup	XP_011519590.1:n.*4723dup
XM_011521289.1:c.*4723dup	XP_011519591.1:n.*4723dup
XM_011521290.1:c.*4723dup	XP_011519592.1:n.*4723dup
XM_005254202.3:c.*4723dup	XP_005254259.1:n.*4723dup
XM_011521289.3:c.*4723dup	XP_011519591.1:n.*4723dup
NM_152594.3:c.*4723dup MANE Select	NP_689807.1:n.*4723dup