Canonical Allele Identifier: CA269293445

Gene: SPRED1

Linked Data

• dbSNP Id: rs111363743
• gnomAD v4: 15-38351150-A-G
• MyVariant Identifiers: chr15:g.38643351A>G (hg19) ; chr15:g.38351150A>G (hg38)
• PubMed: PMID:22753041

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351150A>G , CM000677.2:g.38351150A>G	GRCh38
NC_000015.9:g.38643351A>G , CM000677.1:g.38643351A>G	GRCh37
NC_000015.8:g.36430643A>G	NCBI36
NG_008980.1:g.103300A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.821A>G MANE Select	ENSP00000299084.4:p.Asp274Gly
ENST00000299084.8:c.821A>G	ENSP00000299084.4:p.Asp274Gly
NM_152594.2:c.821A>G	NP_689807.1:p.Asp274Gly
XM_005254202.2:c.857A>G	XP_005254259.1:p.Asp286Gly
XM_005254203.3:c.599A>G	XP_005254260.1:p.Asp200Gly
XM_011521288.1:c.758A>G	XP_011519590.1:p.Asp253Gly
XM_011521289.1:c.758A>G	XP_011519591.1:p.Asp253Gly
XM_011521290.1:c.758A>G	XP_011519592.1:p.Asp253Gly
XM_005254202.3:c.857A>G	XP_005254259.1:p.Asp286Gly
XM_011521289.3:c.758A>G	XP_011519591.1:p.Asp253Gly
NM_152594.3:c.821A>G MANE Select	NP_689807.1:p.Asp274Gly