Canonical Allele Identifier: CA2627714485

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38253246-ATCCCCC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253254_38253259del , CM000677.2:g.38253254_38253259del	GRCh38
NC_000015.9:g.38545455_38545460del , CM000677.1:g.38545455_38545460del	GRCh37
NC_000015.8:g.36332747_36332752del	NCBI36
NG_008980.1:g.5404_5409del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.32+37_32+42del MANE Select	ENSP00000299084.4:n.32+37_32+42del
ENST00000299084.8:c.32+37_32+42del	ENSP00000299084.4:n.32+37_32+42del
ENST00000561205.1:n.370+37_370+42del
ENST00000561317.1:c.-96+37_-96+42del	ENSP00000453680.1:n.-96+37_-96+42del
NM_152594.2:c.32+37_32+42del	NP_689807.1:n.32+37_32+42del
XM_005254202.2:c.32+37_32+42del	XP_005254259.1:n.32+37_32+42del
XM_005254203.3:c.-16+37_-16+42del	XP_005254260.1:n.-16+37_-16+42del
XM_005254202.3:c.32+37_32+42del	XP_005254259.1:n.32+37_32+42del
XR_001751484.1:n.87+315_87+320del
NM_152594.3:c.32+37_32+42del MANE Select	NP_689807.1:n.32+37_32+42del