Canonical Allele Identifier: CA391931821

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38253199-C-A
• MyVariant Identifiers: chr15:g.38545400C>A (hg19) ; chr15:g.38253199C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253199C>A , CM000677.2:g.38253199C>A	GRCh38
NC_000015.9:g.38545400C>A , CM000677.1:g.38545400C>A	GRCh37
NC_000015.8:g.36332692C>A	NCBI36
NG_008980.1:g.5349C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.14C>A MANE Select	ENSP00000299084.4:p.Thr5Lys
ENST00000299084.8:c.14C>A	ENSP00000299084.4:p.Thr5Lys
ENST00000561205.1:n.352C>A
ENST00000561317.1:c.-114C>A	ENSP00000453680.1:n.-114C>A
NM_152594.2:c.14C>A	NP_689807.1:p.Thr5Lys
XM_005254202.2:c.14C>A	XP_005254259.1:p.Thr5Lys
XM_005254203.3:c.-34C>A	XP_005254260.1:n.-34C>A
XM_005254202.3:c.14C>A	XP_005254259.1:p.Thr5Lys
XR_001751484.1:n.87+368G>T
NM_152594.3:c.14C>A MANE Select	NP_689807.1:p.Thr5Lys