Canonical Allele Identifier: CA2627716287

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38351808-T-TGC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351808_38351809insGC , CM000677.2:g.38351808_38351809insGC	GRCh38
NC_000015.9:g.38644009_38644010insGC , CM000677.1:g.38644009_38644010insGC	GRCh37
NC_000015.8:g.36431301_36431302insGC	NCBI36
NG_008980.1:g.103958_103959insGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.*144_*145insGC MANE Select	ENSP00000299084.4:n.*144_*145insGC
ENST00000299084.8:c.*144_*145insGC	ENSP00000299084.4:n.*144_*145insGC
NM_152594.2:c.*144_*145insGC	NP_689807.1:n.*144_*145insGC
XM_005254202.2:c.*144_*145insGC	XP_005254259.1:n.*144_*145insGC
XM_005254203.3:c.*144_*145insGC	XP_005254260.1:n.*144_*145insGC
XM_011521288.1:c.*144_*145insGC	XP_011519590.1:n.*144_*145insGC
XM_011521289.1:c.*144_*145insGC	XP_011519591.1:n.*144_*145insGC
XM_011521290.1:c.*144_*145insGC	XP_011519592.1:n.*144_*145insGC
XM_005254202.3:c.*144_*145insGC	XP_005254259.1:n.*144_*145insGC
XM_011521289.3:c.*144_*145insGC	XP_011519591.1:n.*144_*145insGC
NM_152594.3:c.*144_*145insGC MANE Select	NP_689807.1:n.*144_*145insGC