Canonical Allele Identifier: CA391934435

Gene: SPRED1

Linked Data

• ClinVar Variation Id: 1356671
• ClinVar RCV Id: RCV001876783
• dbSNP Id: rs1345810751
• gnomAD v2: 15-38643705-C-T
• gnomAD v4: 15-38351504-C-T
• COSMIC: COSM5889286
• MyVariant Identifiers: chr15:g.38643705C>T (hg19) ; chr15:g.38351504C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351504C>T , CM000677.2:g.38351504C>T	GRCh38
NC_000015.9:g.38643705C>T , CM000677.1:g.38643705C>T	GRCh37
NC_000015.8:g.36430997C>T	NCBI36
NG_008980.1:g.103654C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.1175C>T MANE Select	ENSP00000299084.4:p.Ser392Leu
ENST00000299084.8:c.1175C>T	ENSP00000299084.4:p.Ser392Leu
NM_152594.2:c.1175C>T	NP_689807.1:p.Ser392Leu
XM_005254202.2:c.1211C>T	XP_005254259.1:p.Ser404Leu
XM_005254203.3:c.953C>T	XP_005254260.1:p.Ser318Leu
XM_011521288.1:c.1112C>T	XP_011519590.1:p.Ser371Leu
XM_011521289.1:c.1112C>T	XP_011519591.1:p.Ser371Leu
XM_011521290.1:c.1112C>T	XP_011519592.1:p.Ser371Leu
XM_005254202.3:c.1211C>T	XP_005254259.1:p.Ser404Leu
XM_011521289.3:c.1112C>T	XP_011519591.1:p.Ser371Leu
NM_152594.3:c.1175C>T MANE Select	NP_689807.1:p.Ser392Leu