Canonical Allele Identifier: CA2627714153
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38252953_38252964del , CM000677.2:g.38252953_38252964del GRCh38
NC_000015.9:g.38545154_38545165del , CM000677.1:g.38545154_38545165del GRCh37
NC_000015.8:g.36332446_36332457del NCBI36
NG_008980.1:g.5103_5114del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-233_-222del MANE Select ENSP00000299084.4:n.-233_-222del
ENST00000299084.8:c.-233_-222del ENSP00000299084.4:n.-233_-222del
ENST00000561205.1:n.106_117del
NM_152594.2:c.-233_-222del NP_689807.1:n.-233_-222del
XM_005254202.2:c.-233_-222del XP_005254259.1:n.-233_-222del
XM_005254203.3:c.-280_-269del XP_005254260.1:n.-280_-269del
XM_005254202.3:c.-233_-222del XP_005254259.1:n.-233_-222del
XR_001751484.1:n.87+607_87+618del
NM_152594.3:c.-233_-222del MANE Select NP_689807.1:n.-233_-222del