Canonical Allele Identifier: CA1406373035

Gene: SPSB4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.141080378_141080380delinsCTG , CM000665.2:g.141080378_141080380delinsCTG	GRCh38
NC_000003.11:g.140799220_140799222delinsCTG , CM000665.1:g.140799220_140799222delinsCTG	GRCh37
NC_000003.10:g.142281910_142281912delinsCTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310546.3:c.694+13580_694+13582delinsCTG MANE Select	ENSP00000311609.2:n.694+13580_694+13582delinsCTG
ENST00000310546.2:c.694+13580_694+13582delinsCTG	ENSP00000311609.2:n.694+13580_694+13582delinsCTG
ENST00000507895.1:n.227_229delinsCTG
ENST00000508126.1:c.161+13580_161+13582delinsCTG
NM_080862.2:c.694+13580_694+13582delinsCTG	NP_543138.1:n.694+13580_694+13582delinsCTG
XM_011513313.1:c.694+13580_694+13582delinsCTG	XP_011511615.1:n.694+13580_694+13582delinsCTG
XR_924215.1:n.1517_1519delinsCTG
XR_924216.1:n.1517_1519delinsCTG
XM_017007509.2:c.*81_*83delinsCTG	XP_016862998.1:n.*81_*83delinsCTG
XR_924215.3:n.998_1000delinsCTG
XR_924216.3:n.998_1000delinsCTG
NM_080862.3:c.694+13580_694+13582delinsCTG MANE Select	NP_543138.1:n.694+13580_694+13582delinsCTG