Canonical Allele Identifier: CA2746290245

Gene: SPTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158612736_158612737insTTTTTTTTT , CM000663.2:g.158612736_158612737insTTTTTTTTT	GRCh38
NC_000001.10:g.158582526_158582527insTTTTTTTTT , CM000663.1:g.158582526_158582527insTTTTTTTTT	GRCh37
NC_000001.9:g.156849150_156849151insTTTTTTTTT	NCBI36
NG_011474.1:g.78986_78987insAAAAAAAAA

Transcript Alleles

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