Canonical Allele Identifier: CA391931823

Gene: SPRED1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.14C>T MANE Select	ENSP00000299084.4:p.Thr5Met
ENST00000299084.8:c.14C>T	ENSP00000299084.4:p.Thr5Met
ENST00000561205.1:n.352C>T
ENST00000561317.1:c.-114C>T	ENSP00000453680.1:n.-114C>T
NM_152594.2:c.14C>T	NP_689807.1:p.Thr5Met
XM_005254202.2:c.14C>T	XP_005254259.1:p.Thr5Met
XM_005254203.3:c.-34C>T	XP_005254260.1:n.-34C>T
XM_005254202.3:c.14C>T	XP_005254259.1:p.Thr5Met
XR_001751484.1:n.87+368G>A
NM_152594.3:c.14C>T MANE Select	NP_689807.1:p.Thr5Met