Canonical Allele Identifier: CA2170788883
Gene: SPRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38299156_38299175delinsCAAGAGTAGTCTTTAAAATA , CM000677.2:g.38299156_38299175delinsCAAGAGTAGTCTTTAAAATA GRCh38
NC_000015.9:g.38591357_38591376delinsCAAGAGTAGTCTTTAAAATA , CM000677.1:g.38591357_38591376delinsCAAGAGTAGTCTTTAAAATA GRCh37
NC_000015.8:g.36378649_36378668delinsCAAGAGTAGTCTTTAAAATA NCBI36
NG_008980.1:g.51306_51325delinsCAAGAGTAGTCTTTAAAATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.33-217_33-198delinsCAAGAGTAGTCTTTAAAATA MANE Select ENSP00000299084.4:n.33-217_33-198delinsCAAGAGTAGTCTTTAAAATA
ENST00000299084.8:c.33-217_33-198delinsCAAGAGTAGTCTTTAAAATA ENSP00000299084.4:n.33-217_33-198delinsCAAGAGTAGTCTTTAAAATA
ENST00000561205.1:n.371-217_371-198delinsCAAGAGTAGTCTTTAAAATA
ENST00000561317.1:c.-31-217_-31-198delinsCAAGAGTAGTCTTTAAAATA ENSP00000453680.1:n.-31-217_-31-198delinsCAAGAGTAGTCTTTAAAATA...
NM_152594.2:c.33-217_33-198delinsCAAGAGTAGTCTTTAAAATA NP_689807.1:n.33-217_33-198delinsCAAGAGTAGTCTTTAAAATA
XM_005254202.2:c.69-217_69-198delinsCAAGAGTAGTCTTTAAAATA XP_005254259.1:n.69-217_69-198delinsCAAGAGTAGTCTTTAAAATA
XM_005254203.3:c.-15-23085_-15-23066delinsCAAGAGTAGTCTTTAAAATA XP_005254260.1:n.-15-23085_-15-23066delinsCAAGAGTAGTCTTTAAAAT...
XM_011521288.1:c.-31-217_-31-198delinsCAAGAGTAGTCTTTAAAATA XP_011519590.1:n.-31-217_-31-198delinsCAAGAGTAGTCTTTAAAATA
XM_011521289.1:c.-31-217_-31-198delinsCAAGAGTAGTCTTTAAAATA XP_011519591.1:n.-31-217_-31-198delinsCAAGAGTAGTCTTTAAAATA
XM_011521290.1:c.-31-217_-31-198delinsCAAGAGTAGTCTTTAAAATA XP_011519592.1:n.-31-217_-31-198delinsCAAGAGTAGTCTTTAAAATA
XM_005254202.3:c.69-217_69-198delinsCAAGAGTAGTCTTTAAAATA XP_005254259.1:n.69-217_69-198delinsCAAGAGTAGTCTTTAAAATA
XM_011521289.3:c.-31-217_-31-198delinsCAAGAGTAGTCTTTAAAATA XP_011519591.1:n.-31-217_-31-198delinsCAAGAGTAGTCTTTAAAATA
NM_152594.3:c.33-217_33-198delinsCAAGAGTAGTCTTTAAAATA MANE Select NP_689807.1:n.33-217_33-198delinsCAAGAGTAGTCTTTAAAATA