Canonical Allele Identifier: CA2627714196

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38252984-TGCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38252988_38252990del , CM000677.2:g.38252988_38252990del	GRCh38
NC_000015.9:g.38545189_38545191del , CM000677.1:g.38545189_38545191del	GRCh37
NC_000015.8:g.36332481_36332483del	NCBI36
NG_008980.1:g.5138_5140del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.-198_-196del MANE Select	ENSP00000299084.4:n.-198_-196del
ENST00000299084.8:c.-198_-196del	ENSP00000299084.4:n.-198_-196del
ENST00000561205.1:n.141_143del
NM_152594.2:c.-198_-196del	NP_689807.1:n.-198_-196del
XM_005254202.2:c.-198_-196del	XP_005254259.1:n.-198_-196del
XM_005254203.3:c.-245_-243del	XP_005254260.1:n.-245_-243del
XM_005254202.3:c.-198_-196del	XP_005254259.1:n.-198_-196del
XR_001751484.1:n.87+580_87+582del
NM_152594.3:c.-198_-196del MANE Select	NP_689807.1:n.-198_-196del