Canonical Allele Identifier: CA968818191

Gene: SPRED1

Linked Data

• gnomAD v3: 15-38352097-AG-A
• gnomAD v4: 15-38352097-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38352098del , CM000677.2:g.38352098del	GRCh38
NC_000015.9:g.38644299del , CM000677.1:g.38644299del	GRCh37
NC_000015.8:g.36431591del	NCBI36
NG_008980.1:g.104248del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.*434del MANE Select	ENSP00000299084.4:n.*434del
ENST00000299084.8:c.*434del	ENSP00000299084.4:n.*434del
NM_152594.2:c.*434del	NP_689807.1:n.*434del
XM_005254202.2:c.*434del	XP_005254259.1:n.*434del
XM_005254203.3:c.*434del	XP_005254260.1:n.*434del
XM_011521288.1:c.*434del	XP_011519590.1:n.*434del
XM_011521289.1:c.*434del	XP_011519591.1:n.*434del
XM_011521290.1:c.*434del	XP_011519592.1:n.*434del
XM_005254202.3:c.*434del	XP_005254259.1:n.*434del
XM_011521289.3:c.*434del	XP_011519591.1:n.*434del
NM_152594.3:c.*434del MANE Select	NP_689807.1:n.*434del