Canonical Allele Identifier: CA391931836

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38545408T>A (hg19) ; chr15:g.38253207T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253207T>A , CM000677.2:g.38253207T>A	GRCh38
NC_000015.9:g.38545408T>A , CM000677.1:g.38545408T>A	GRCh37
NC_000015.8:g.36332700T>A	NCBI36
NG_008980.1:g.5357T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.22T>A MANE Select	ENSP00000299084.4:p.Ser8Thr
ENST00000299084.8:c.22T>A	ENSP00000299084.4:p.Ser8Thr
ENST00000561205.1:n.360T>A
ENST00000561317.1:c.-106T>A	ENSP00000453680.1:n.-106T>A
NM_152594.2:c.22T>A	NP_689807.1:p.Ser8Thr
XM_005254202.2:c.22T>A	XP_005254259.1:p.Ser8Thr
XM_005254203.3:c.-26T>A	XP_005254260.1:n.-26T>A
XM_005254202.3:c.22T>A	XP_005254259.1:p.Ser8Thr
XR_001751484.1:n.87+360A>T
NM_152594.3:c.22T>A MANE Select	NP_689807.1:p.Ser8Thr