Canonical Allele Identifier: CA968807125

Gene: SPRED1

Linked Data

• dbSNP Id: rs1894008310
• gnomAD v3: 15-38252896-CTT-C
• gnomAD v4: 15-38252896-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38252900_38252901del , CM000677.2:g.38252900_38252901del	GRCh38
NC_000015.9:g.38545101_38545102del , CM000677.1:g.38545101_38545102del	GRCh37
NC_000015.8:g.36332393_36332394del	NCBI36
NG_008980.1:g.5050_5051del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.-286_-285del MANE Select	ENSP00000299084.4:n.-286_-285del
ENST00000299084.8:c.-286_-285del	ENSP00000299084.4:n.-286_-285del
ENST00000561205.1:n.53_54del
NM_152594.2:c.-286_-285del	NP_689807.1:n.-286_-285del
XM_005254202.2:c.-286_-285del	XP_005254259.1:n.-286_-285del
XM_005254203.3:c.-333_-332del	XP_005254260.1:n.-333_-332del
XM_005254202.3:c.-286_-285del	XP_005254259.1:n.-286_-285del
XR_001751484.1:n.87+669_87+670del
NM_152594.3:c.-286_-285del MANE Select	NP_689807.1:n.-286_-285del