Canonical Allele Identifier: CA391931833

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38253205-C-A
• MyVariant Identifiers: chr15:g.38545406C>A (hg19) ; chr15:g.38253205C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253205C>A , CM000677.2:g.38253205C>A	GRCh38
NC_000015.9:g.38545406C>A , CM000677.1:g.38545406C>A	GRCh37
NC_000015.8:g.36332698C>A	NCBI36
NG_008980.1:g.5355C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.20C>A MANE Select	ENSP00000299084.4:p.Thr7Asn
ENST00000299084.8:c.20C>A	ENSP00000299084.4:p.Thr7Asn
ENST00000561205.1:n.358C>A
ENST00000561317.1:c.-108C>A	ENSP00000453680.1:n.-108C>A
NM_152594.2:c.20C>A	NP_689807.1:p.Thr7Asn
XM_005254202.2:c.20C>A	XP_005254259.1:p.Thr7Asn
XM_005254203.3:c.-28C>A	XP_005254260.1:n.-28C>A
XM_005254202.3:c.20C>A	XP_005254259.1:p.Thr7Asn
XR_001751484.1:n.87+362G>T
NM_152594.3:c.20C>A MANE Select	NP_689807.1:p.Thr7Asn