Canonical Allele Identifier: CA2746290247
Gene: SPTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.158612736_158612737insTTTTTTTTTTTAC , CM000663.2:g.158612736_158612737insTTTTTTTTTTTAC GRCh38
NC_000001.10:g.158582526_158582527insTTTTTTTTTTTAC , CM000663.1:g.158582526_158582527insTTTTTTTTTTTAC GRCh37
NC_000001.9:g.156849150_156849151insTTTTTTTTTTTAC NCBI36
NG_011474.1:g.78980_78981insGTAAAAAAAAAAA

Transcript Alleles

HGVS Amino-acid change
ENST00000643759.2:c.7134+80_7134+81insGTAAAAAAAAAAA MANE Select ENSP00000495214.1:n.7134+80_7134+81insGTAAAAAAAAAAA
ENST00000368147.8:c.7134+80_7134+81insGTAAAAAAAAAAA ENSP00000357129.4:n.7134+80_7134+81insGTAAAAAAAAAAA
ENST00000614909.4:c.7134+80_7134+81insGTAAAAAAAAAAA ENSP00000482595.1:n.7134+80_7134+81insGTAAAAAAAAAAA
NM_003126.2:c.7134+80_7134+81insGTAAAAAAAAAAA NP_003117.2:n.7134+80_7134+81insGTAAAAAAAAAAA
XM_011509916.1:c.7134+80_7134+81insGTAAAAAAAAAAA XP_011508218.1:n.7134+80_7134+81insGTAAAAAAAAAAA
XM_011509917.1:c.7116+80_7116+81insGTAAAAAAAAAAA XP_011508219.1:n.7116+80_7116+81insGTAAAAAAAAAAA
NM_003126.3:c.7134+80_7134+81insGTAAAAAAAAAAA NP_003117.2:n.7134+80_7134+81insGTAAAAAAAAAAA
XM_011509916.2:c.7134+80_7134+81insGTAAAAAAAAAAA XP_011508218.1:n.7134+80_7134+81insGTAAAAAAAAAAA
XM_011509917.3:c.7116+80_7116+81insGTAAAAAAAAAAA XP_011508219.1:n.7116+80_7116+81insGTAAAAAAAAAAA
NM_003126.4:c.7134+80_7134+81insGTAAAAAAAAAAA MANE Select NP_003117.2:n.7134+80_7134+81insGTAAAAAAAAAAA