Canonical Allele Identifier: CA391934354

Gene: SPRED1

Linked Data

• ClinVar Variation Id: 1400180
• ClinVar RCV Id: RCV001918061 ; RCV004041731
• dbSNP Id: rs1261567261
• gnomAD v2: 15-38591698-A-G
• gnomAD v3: 15-38299497-A-G
• gnomAD v4: 15-38299497-A-G
• MyVariant Identifiers: chr15:g.38591698A>G (hg19) ; chr15:g.38299497A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299497A>G , CM000677.2:g.38299497A>G	GRCh38
NC_000015.9:g.38591698A>G , CM000677.1:g.38591698A>G	GRCh37
NC_000015.8:g.36378990A>G	NCBI36
NG_008980.1:g.51647A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.157A>G MANE Select	ENSP00000299084.4:p.Asn53Asp
ENST00000299084.8:c.157A>G	ENSP00000299084.4:p.Asn53Asp
ENST00000561205.1:n.495A>G
ENST00000561317.1:c.94A>G	ENSP00000453680.1:p.Asn32Asp
NM_152594.2:c.157A>G	NP_689807.1:p.Asn53Asp
XM_005254202.2:c.193A>G	XP_005254259.1:p.Asn65Asp
XM_005254203.3:c.-15-22744A>G	XP_005254260.1:n.-15-22744A>G
XM_011521288.1:c.94A>G	XP_011519590.1:p.Asn32Asp
XM_011521289.1:c.94A>G	XP_011519591.1:p.Asn32Asp
XM_011521290.1:c.94A>G	XP_011519592.1:p.Asn32Asp
XM_005254202.3:c.193A>G	XP_005254259.1:p.Asn65Asp
XM_011521289.3:c.94A>G	XP_011519591.1:p.Asn32Asp
NM_152594.3:c.157A>G MANE Select	NP_689807.1:p.Asn53Asp