Canonical Allele Identifier: CA1201536863

Gene: SPTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158612730_158612731delinsGT , CM000663.2:g.158612730_158612731delinsGT	GRCh38
NC_000001.10:g.158582520_158582521delinsGT , CM000663.1:g.158582520_158582521delinsGT	GRCh37
NC_000001.9:g.156849144_156849145delinsGT	NCBI36
NG_011474.1:g.78986_78987delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000643759.2:c.7134+86_7134+87delinsAC MANE Select	ENSP00000495214.1:n.7134+86_7134+87delins...
ENST00000368147.8:c.7134+86_7134+87delinsAC	ENSP00000357129.4:n.7134+86_7134+87delins...
ENST00000614909.4:c.7134+86_7134+87delinsAC	ENSP00000482595.1:n.7134+86_7134+87delins...
NM_003126.2:c.7134+86_7134+87delinsAC	NP_003117.2:n.7134+86_7134+87delinsAC
XM_011509916.1:c.7134+86_7134+87delinsAC	XP_011508218.1:n.7134+86_7134+87delinsAC
XM_011509917.1:c.7116+86_7116+87delinsAC	XP_011508219.1:n.7116+86_7116+87delinsAC
NM_003126.3:c.7134+86_7134+87delinsAC	NP_003117.2:n.7134+86_7134+87delinsAC
XM_011509916.2:c.7134+86_7134+87delinsAC	XP_011508218.1:n.7134+86_7134+87delinsAC
XM_011509917.3:c.7116+86_7116+87delinsAC	XP_011508219.1:n.7116+86_7116+87delinsAC
NM_003126.4:c.7134+86_7134+87delinsAC MANE Select	NP_003117.2:n.7134+86_7134+87delinsAC