Canonical Allele Identifier: CA2627714406

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38253138-GCCTGCTGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253139_38253146del , CM000677.2:g.38253139_38253146del	GRCh38
NC_000015.9:g.38545340_38545347del , CM000677.1:g.38545340_38545347del	GRCh37
NC_000015.8:g.36332632_36332639del	NCBI36
NG_008980.1:g.5289_5296del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.-47_-40del MANE Select	ENSP00000299084.4:n.-47_-40del
ENST00000299084.8:c.-47_-40del	ENSP00000299084.4:n.-47_-40del
ENST00000561205.1:n.292_299del
NM_152594.2:c.-47_-40del	NP_689807.1:n.-47_-40del
XM_005254202.2:c.-47_-40del	XP_005254259.1:n.-47_-40del
XM_005254203.3:c.-94_-87del	XP_005254260.1:n.-94_-87del
XM_005254202.3:c.-47_-40del	XP_005254259.1:n.-47_-40del
XR_001751484.1:n.87+421_87+428del
NM_152594.3:c.-47_-40del MANE Select	NP_689807.1:n.-47_-40del