Canonical Allele Identifier: CA2627714458

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38253185-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253185G>A , CM000677.2:g.38253185G>A	GRCh38
NC_000015.9:g.38545386G>A , CM000677.1:g.38545386G>A	GRCh37
NC_000015.8:g.36332678G>A	NCBI36
NG_008980.1:g.5335G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.-1G>A MANE Select	ENSP00000299084.4:n.-1G>A
ENST00000299084.8:c.-1G>A	ENSP00000299084.4:n.-1G>A
ENST00000561205.1:n.338G>A
ENST00000561317.1:c.-128G>A	ENSP00000453680.1:n.-128G>A
NM_152594.2:c.-1G>A	NP_689807.1:n.-1G>A
XM_005254202.2:c.-1G>A	XP_005254259.1:n.-1G>A
XM_005254203.3:c.-48G>A	XP_005254260.1:n.-48G>A
XM_005254202.3:c.-1G>A	XP_005254259.1:n.-1G>A
XR_001751484.1:n.87+382C>T
NM_152594.3:c.-1G>A MANE Select	NP_689807.1:n.-1G>A