Canonical Allele Identifier: CA2803803439
Gene: SPRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253081_38253106del , CM000677.2:g.38253081_38253106del GRCh38
NC_000015.9:g.38545282_38545307del , CM000677.1:g.38545282_38545307del GRCh37
NC_000015.8:g.36332574_36332599del NCBI36
NG_008980.1:g.5231_5256del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-105_-80del MANE Select ENSP00000299084.4:n.-105_-80del
ENST00000299084.8:c.-105_-80del ENSP00000299084.4:n.-105_-80del
ENST00000561205.1:n.234_259del
NM_152594.2:c.-105_-80del NP_689807.1:n.-105_-80del
XM_005254202.2:c.-105_-80del XP_005254259.1:n.-105_-80del
XM_005254203.3:c.-152_-127del XP_005254260.1:n.-152_-127del
XM_005254202.3:c.-105_-80del XP_005254259.1:n.-105_-80del
XR_001751484.1:n.87+470_87+495del
NM_152594.3:c.-105_-80del MANE Select NP_689807.1:n.-105_-80del