Canonical Allele Identifier: CA391933692

Gene: SPRED1

Linked Data

• dbSNP Id: rs1888479856
• MyVariant Identifiers: chr15:g.38643517T>A (hg19) ; chr15:g.38351316T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351316T>A , CM000677.2:g.38351316T>A	GRCh38
NC_000015.9:g.38643517T>A , CM000677.1:g.38643517T>A	GRCh37
NC_000015.8:g.36430809T>A	NCBI36
NG_008980.1:g.103466T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.987T>A MANE Select	ENSP00000299084.4:p.Asp329Glu
ENST00000299084.8:c.987T>A	ENSP00000299084.4:p.Asp329Glu
NM_152594.2:c.987T>A	NP_689807.1:p.Asp329Glu
XM_005254202.2:c.1023T>A	XP_005254259.1:p.Asp341Glu
XM_005254203.3:c.765T>A	XP_005254260.1:p.Asp255Glu
XM_011521288.1:c.924T>A	XP_011519590.1:p.Asp308Glu
XM_011521289.1:c.924T>A	XP_011519591.1:p.Asp308Glu
XM_011521290.1:c.924T>A	XP_011519592.1:p.Asp308Glu
XM_005254202.3:c.1023T>A	XP_005254259.1:p.Asp341Glu
XM_011521289.3:c.924T>A	XP_011519591.1:p.Asp308Glu
NM_152594.3:c.987T>A MANE Select	NP_689807.1:p.Asp329Glu