Canonical Allele Identifier: CA2575673305

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38350934-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38350936del , CM000677.2:g.38350936del	GRCh38
NC_000015.9:g.38643137del , CM000677.1:g.38643137del	GRCh37
NC_000015.8:g.36430429del	NCBI36
NG_008980.1:g.103086del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.685-78del MANE Select	ENSP00000299084.4:n.685-78del
ENST00000299084.8:c.685-78del	ENSP00000299084.4:n.685-78del
NM_152594.2:c.685-78del	NP_689807.1:n.685-78del
XM_005254202.2:c.721-78del	XP_005254259.1:n.721-78del
XM_005254203.3:c.463-78del	XP_005254260.1:n.463-78del
XM_011521288.1:c.622-78del	XP_011519590.1:n.622-78del
XM_011521289.1:c.622-78del	XP_011519591.1:n.622-78del
XM_011521290.1:c.622-78del	XP_011519592.1:n.622-78del
XM_005254202.3:c.721-78del	XP_005254259.1:n.721-78del
XM_011521289.3:c.622-78del	XP_011519591.1:n.622-78del
NM_152594.3:c.685-78del MANE Select	NP_689807.1:n.685-78del