Canonical Allele Identifier: CA617506046

Gene: SPRED1

Linked Data

• dbSNP Id: rs1442935138
• gnomAD v2: 15-38643966-TATC-T
• gnomAD v3: 15-38351765-TATC-T
• gnomAD v4: 15-38351765-TATC-T
• MyVariant Identifiers: chr15:g.38643967_38643969del (hg19) ; chr15:g.38351766_38351768del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351768_38351770del , CM000677.2:g.38351768_38351770del	GRCh38
NC_000015.9:g.38643969_38643971del , CM000677.1:g.38643969_38643971del	GRCh37
NC_000015.8:g.36431261_36431263del	NCBI36
NG_008980.1:g.103918_103920del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.*104_*106del MANE Select	ENSP00000299084.4:n.*104_*106del
ENST00000299084.8:c.*104_*106del	ENSP00000299084.4:n.*104_*106del
NM_152594.2:c.*104_*106del	NP_689807.1:n.*104_*106del
XM_005254202.2:c.*104_*106del	XP_005254259.1:n.*104_*106del
XM_005254203.3:c.*104_*106del	XP_005254260.1:n.*104_*106del
XM_011521288.1:c.*104_*106del	XP_011519590.1:n.*104_*106del
XM_011521289.1:c.*104_*106del	XP_011519591.1:n.*104_*106del
XM_011521290.1:c.*104_*106del	XP_011519592.1:n.*104_*106del
XM_005254202.3:c.*104_*106del	XP_005254259.1:n.*104_*106del
XM_011521289.3:c.*104_*106del	XP_011519591.1:n.*104_*106del
NM_152594.3:c.*104_*106del MANE Select	NP_689807.1:n.*104_*106del