Canonical Allele Identifier: CA16606924

Gene: SPRED1

Linked Data

• ClinVar Variation Id: 387693
• ClinVar RCV Id: RCV000424209
• dbSNP Id: rs1057522873
• MyVariant Identifiers: chr15:g.38643463T>C (hg19) ; chr15:g.38351262T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351262T>C , CM000677.2:g.38351262T>C	GRCh38
NC_000015.9:g.38643463T>C , CM000677.1:g.38643463T>C	GRCh37
NC_000015.8:g.36430755T>C	NCBI36
NG_008980.1:g.103412T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.933T>C MANE Select	ENSP00000299084.4:p.Phe311=
ENST00000299084.8:c.933T>C	ENSP00000299084.4:p.Phe311=
NM_152594.2:c.933T>C	NP_689807.1:p.Phe311=
XM_005254202.2:c.969T>C	XP_005254259.1:p.Phe323=
XM_005254203.3:c.711T>C	XP_005254260.1:p.Phe237=
XM_011521288.1:c.870T>C	XP_011519590.1:p.Phe290=
XM_011521289.1:c.870T>C	XP_011519591.1:p.Phe290=
XM_011521290.1:c.870T>C	XP_011519592.1:p.Phe290=
XM_005254202.3:c.969T>C	XP_005254259.1:p.Phe323=
XM_011521289.3:c.870T>C	XP_011519591.1:p.Phe290=
NM_152594.3:c.933T>C MANE Select	NP_689807.1:p.Phe311=