Canonical Allele Identifier: CA913993912
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38352247_38352248insGTAT , CM000677.2:g.38352247_38352248insGTAT GRCh38
NC_000015.9:g.38644448_38644449insGTAT , CM000677.1:g.38644448_38644449insGTAT GRCh37
NC_000015.8:g.36431740_36431741insGTAT NCBI36
NG_008980.1:g.104397_104398insGTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.*583_*584insGTAT MANE Select ENSP00000299084.4:n.*583_*584insGTAT
ENST00000299084.8:c.*583_*584insGTAT ENSP00000299084.4:n.*583_*584insGTAT
NM_152594.2:c.*583_*584insGTAT NP_689807.1:n.*583_*584insGTAT
XM_005254202.2:c.*583_*584insGTAT XP_005254259.1:n.*583_*584insGTAT
XM_005254203.3:c.*583_*584insGTAT XP_005254260.1:n.*583_*584insGTAT
XM_011521288.1:c.*583_*584insGTAT XP_011519590.1:n.*583_*584insGTAT
XM_011521289.1:c.*583_*584insGTAT XP_011519591.1:n.*583_*584insGTAT
XM_011521290.1:c.*583_*584insGTAT XP_011519592.1:n.*583_*584insGTAT
XM_005254202.3:c.*583_*584insGTAT XP_005254259.1:n.*583_*584insGTAT
XM_011521289.3:c.*583_*584insGTAT XP_011519591.1:n.*583_*584insGTAT
NM_152594.3:c.*583_*584insGTAT MANE Select NP_689807.1:n.*583_*584insGTAT