Canonical Allele Identifier: CA1201536899

Gene: SPTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158612794_158612795delinsAG , CM000663.2:g.158612794_158612795delinsAG	GRCh38
NC_000001.10:g.158582584_158582585delinsAG , CM000663.1:g.158582584_158582585delinsAG	GRCh37
NC_000001.9:g.156849208_156849209delinsAG	NCBI36
NG_011474.1:g.78922_78923delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.7134+22_7134+23delinsCT MANE Select	ENSP00000495214.1:n.7134+22_7134+23delinsCT
ENST00000368147.8:c.7134+22_7134+23delinsCT	ENSP00000357129.4:n.7134+22_7134+23delinsCT
ENST00000481212.5:n.597_598delinsCT
ENST00000498708.1:n.588_589delinsCT
ENST00000614909.4:c.7134+22_7134+23delinsCT	ENSP00000482595.1:n.7134+22_7134+23delinsCT
NM_003126.2:c.7134+22_7134+23delinsCT	NP_003117.2:n.7134+22_7134+23delinsCT
XM_011509916.1:c.7134+22_7134+23delinsCT	XP_011508218.1:n.7134+22_7134+23delinsCT
XM_011509917.1:c.7116+22_7116+23delinsCT	XP_011508219.1:n.7116+22_7116+23delinsCT
NM_003126.3:c.7134+22_7134+23delinsCT	NP_003117.2:n.7134+22_7134+23delinsCT
XM_011509916.2:c.7134+22_7134+23delinsCT	XP_011508218.1:n.7134+22_7134+23delinsCT
XM_011509917.3:c.7116+22_7116+23delinsCT	XP_011508219.1:n.7116+22_7116+23delinsCT
NM_003126.4:c.7134+22_7134+23delinsCT MANE Select	NP_003117.2:n.7134+22_7134+23delinsCT