Canonical Allele Identifier: CA617495168

Gene: SPRED1

Linked Data

• dbSNP Id: rs1364084018
• gnomAD v2: 15-38545322-GCTGCTGTTGCTCCCCCGC-G
• gnomAD v3: 15-38253121-GCTGCTGTTGCTCCCCCGC-G
• gnomAD v4: 15-38253121-GCTGCTGTTGCTCCCCCGC-G
• MyVariant Identifiers: chr15:g.38545323_38545340del (hg19) ; chr15:g.38253122_38253139del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253135_38253152del , CM000677.2:g.38253135_38253152del	GRCh38
NC_000015.9:g.38545336_38545353del , CM000677.1:g.38545336_38545353del	GRCh37
NC_000015.8:g.36332628_36332645del	NCBI36
NG_008980.1:g.5285_5302del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.-51_-34del MANE Select	ENSP00000299084.4:n.-51_-34del
ENST00000299084.8:c.-51_-34del	ENSP00000299084.4:n.-51_-34del
ENST00000561205.1:n.288_305del
NM_152594.2:c.-51_-34del	NP_689807.1:n.-51_-34del
XM_005254202.2:c.-51_-34del	XP_005254259.1:n.-51_-34del
XM_005254203.3:c.-98_-81del	XP_005254260.1:n.-98_-81del
XM_005254202.3:c.-51_-34del	XP_005254259.1:n.-51_-34del
XR_001751484.1:n.87+428_87+445del
NM_152594.3:c.-51_-34del MANE Select	NP_689807.1:n.-51_-34del