Canonical Allele Identifier: CA2627716460

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38352133-T-TGGGAA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38352133_38352134insGGGAA , CM000677.2:g.38352133_38352134insGGGAA	GRCh38
NC_000015.9:g.38644334_38644335insGGGAA , CM000677.1:g.38644334_38644335insGGGAA	GRCh37
NC_000015.8:g.36431626_36431627insGGGAA	NCBI36
NG_008980.1:g.104283_104284insGGGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.*469_*470insGGGAA MANE Select	ENSP00000299084.4:n.*469_*470insGGGAA
ENST00000299084.8:c.*469_*470insGGGAA	ENSP00000299084.4:n.*469_*470insGGGAA
NM_152594.2:c.*469_*470insGGGAA	NP_689807.1:n.*469_*470insGGGAA
XM_005254202.2:c.*469_*470insGGGAA	XP_005254259.1:n.*469_*470insGGGAA
XM_005254203.3:c.*469_*470insGGGAA	XP_005254260.1:n.*469_*470insGGGAA
XM_011521288.1:c.*469_*470insGGGAA	XP_011519590.1:n.*469_*470insGGGAA
XM_011521289.1:c.*469_*470insGGGAA	XP_011519591.1:n.*469_*470insGGGAA
XM_011521290.1:c.*469_*470insGGGAA	XP_011519592.1:n.*469_*470insGGGAA
XM_005254202.3:c.*469_*470insGGGAA	XP_005254259.1:n.*469_*470insGGGAA
XM_011521289.3:c.*469_*470insGGGAA	XP_011519591.1:n.*469_*470insGGGAA
NM_152594.3:c.*469_*470insGGGAA MANE Select	NP_689807.1:n.*469_*470insGGGAA