Canonical Allele Identifier: CA391931847

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38253212-C-A
• MyVariant Identifiers: chr15:g.38545413C>A (hg19) ; chr15:g.38253212C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253212C>A , CM000677.2:g.38253212C>A	GRCh38
NC_000015.9:g.38545413C>A , CM000677.1:g.38545413C>A	GRCh37
NC_000015.8:g.36332705C>A	NCBI36
NG_008980.1:g.5362C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.27C>A MANE Select	ENSP00000299084.4:p.Asp9Glu
ENST00000299084.8:c.27C>A	ENSP00000299084.4:p.Asp9Glu
ENST00000561205.1:n.365C>A
ENST00000561317.1:c.-101C>A	ENSP00000453680.1:n.-101C>A
NM_152594.2:c.27C>A	NP_689807.1:p.Asp9Glu
XM_005254202.2:c.27C>A	XP_005254259.1:p.Asp9Glu
XM_005254203.3:c.-21C>A	XP_005254260.1:n.-21C>A
XM_005254202.3:c.27C>A	XP_005254259.1:p.Asp9Glu
XR_001751484.1:n.87+355G>T
NM_152594.3:c.27C>A MANE Select	NP_689807.1:p.Asp9Glu