Canonical Allele Identifier: CA655954296

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38299267-C-A
• COSMIC: COSN6272180

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299267C>A , CM000677.2:g.38299267C>A	GRCh38
NC_000015.9:g.38591468C>A , CM000677.1:g.38591468C>A	GRCh37
NC_000015.8:g.36378760C>A	NCBI36
NG_008980.1:g.51417C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.33-106C>A MANE Select	ENSP00000299084.4:n.33-106C>A
ENST00000299084.8:c.33-106C>A	ENSP00000299084.4:n.33-106C>A
ENST00000561205.1:n.371-106C>A
ENST00000561317.1:c.-31-106C>A	ENSP00000453680.1:n.-31-106C>A
NM_152594.2:c.33-106C>A	NP_689807.1:n.33-106C>A
XM_005254202.2:c.69-106C>A	XP_005254259.1:n.69-106C>A
XM_005254203.3:c.-15-22974C>A	XP_005254260.1:n.-15-22974C>A
XM_011521288.1:c.-31-106C>A	XP_011519590.1:n.-31-106C>A
XM_011521289.1:c.-31-106C>A	XP_011519591.1:n.-31-106C>A
XM_011521290.1:c.-31-106C>A	XP_011519592.1:n.-31-106C>A
XM_005254202.3:c.69-106C>A	XP_005254259.1:n.69-106C>A
XM_011521289.3:c.-31-106C>A	XP_011519591.1:n.-31-106C>A
NM_152594.3:c.33-106C>A MANE Select	NP_689807.1:n.33-106C>A