Canonical Allele Identifier: CA617500599

Gene: SPRED1

Linked Data

• dbSNP Id: rs1235148954
• gnomAD v2: 15-38591539-GA-G
• gnomAD v4: 15-38299338-GA-G
• MyVariant Identifiers: chr15:g.38591540del (hg19) ; chr15:g.38299339del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299342del , CM000677.2:g.38299342del	GRCh38
NC_000015.9:g.38591543del , CM000677.1:g.38591543del	GRCh37
NC_000015.8:g.36378835del	NCBI36
NG_008980.1:g.51492del

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.33-31del MANE Select	ENSP00000299084.4:n.33-31del
ENST00000299084.8:c.33-31del	ENSP00000299084.4:n.33-31del
ENST00000561205.1:n.371-31del
ENST00000561317.1:c.-31-31del	ENSP00000453680.1:n.-31-31del
NM_152594.2:c.33-31del	NP_689807.1:n.33-31del
XM_005254202.2:c.69-31del	XP_005254259.1:n.69-31del
XM_005254203.3:c.-15-22899del	XP_005254260.1:n.-15-22899del
XM_011521288.1:c.-31-31del	XP_011519590.1:n.-31-31del
XM_011521289.1:c.-31-31del	XP_011519591.1:n.-31-31del
XM_011521290.1:c.-31-31del	XP_011519592.1:n.-31-31del
XM_005254202.3:c.69-31del	XP_005254259.1:n.69-31del
XM_011521289.3:c.-31-31del	XP_011519591.1:n.-31-31del
NM_152594.3:c.33-31del MANE Select	NP_689807.1:n.33-31del