Canonical Allele Identifier: CA2170789080
Gene: SPRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38299654_38299666delinsATGTTTCTGGAGC , CM000677.2:g.38299654_38299666delinsATGTTTCTGGAGC GRCh38
NC_000015.9:g.38591855_38591867delinsATGTTTCTGGAGC , CM000677.1:g.38591855_38591867delinsATGTTTCTGGAGC GRCh37
NC_000015.8:g.36379147_36379159delinsATGTTTCTGGAGC NCBI36
NG_008980.1:g.51804_51816delinsATGTTTCTGGAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.207+107_207+119delinsATGTTTCTGGAGC MANE Select ENSP00000299084.4:n.207+107_207+119delinsATGTTTCTGGAGC
ENST00000299084.8:c.207+107_207+119delinsATGTTTCTGGAGC ENSP00000299084.4:n.207+107_207+119delinsATGTTTCTGGAGC
ENST00000561205.1:n.545+107_545+119delinsATGTTTCTGGAGC
ENST00000561317.1:c.144+107_144+119delinsATGTTTCTGGAGC ENSP00000453680.1:n.144+107_144+119delinsATGTTTCTGGAGC
NM_152594.2:c.207+107_207+119delinsATGTTTCTGGAGC NP_689807.1:n.207+107_207+119delinsATGTTTCTGGAGC
XM_005254202.2:c.243+107_243+119delinsATGTTTCTGGAGC XP_005254259.1:n.243+107_243+119delinsATGTTTCTGGAGC
XM_005254203.3:c.-15-22587_-15-22575delinsATGTTTCTGGAGC XP_005254260.1:n.-15-22587_-15-22575delinsATGTTTCTGGAGC
XM_011521288.1:c.144+107_144+119delinsATGTTTCTGGAGC XP_011519590.1:n.144+107_144+119delinsATGTTTCTGGAGC
XM_011521289.1:c.144+107_144+119delinsATGTTTCTGGAGC XP_011519591.1:n.144+107_144+119delinsATGTTTCTGGAGC
XM_011521290.1:c.144+107_144+119delinsATGTTTCTGGAGC XP_011519592.1:n.144+107_144+119delinsATGTTTCTGGAGC
XM_005254202.3:c.243+107_243+119delinsATGTTTCTGGAGC XP_005254259.1:n.243+107_243+119delinsATGTTTCTGGAGC
XM_011521289.3:c.144+107_144+119delinsATGTTTCTGGAGC XP_011519591.1:n.144+107_144+119delinsATGTTTCTGGAGC
NM_152594.3:c.207+107_207+119delinsATGTTTCTGGAGC MANE Select NP_689807.1:n.207+107_207+119delinsATGTTTCTGGAGC