Canonical Allele Identifier: CA2648555390

Gene: SPTA1

Linked Data

• gnomAD v4: 1-158612572-T-TAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158612573_158612574insAAAA , CM000663.2:g.158612573_158612574insAAAA	GRCh38
NC_000001.10:g.158582363_158582364insAAAA , CM000663.1:g.158582363_158582364insAAAA	GRCh37
NC_000001.9:g.156848987_156848988insAAAA	NCBI36
NG_011474.1:g.79144_79145insTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.7134+244_7134+245insTTTT MANE Select	ENSP00000495214.1:n.7134+244_7134+245insTTTT
ENST00000368147.8:c.7134+244_7134+245insTTTT	ENSP00000357129.4:n.7134+244_7134+245insTTTT
ENST00000614909.4:c.7134+244_7134+245insTTTT	ENSP00000482595.1:n.7134+244_7134+245insTTTT
NM_003126.2:c.7134+244_7134+245insTTTT	NP_003117.2:n.7134+244_7134+245insTTTT
XM_011509916.1:c.7134+244_7134+245insTTTT	XP_011508218.1:n.7134+244_7134+245insTTTT
XM_011509917.1:c.7116+244_7116+245insTTTT	XP_011508219.1:n.7116+244_7116+245insTTTT
NM_003126.3:c.7134+244_7134+245insTTTT	NP_003117.2:n.7134+244_7134+245insTTTT
XM_011509916.2:c.7134+244_7134+245insTTTT	XP_011508218.1:n.7134+244_7134+245insTTTT
XM_011509917.3:c.7116+244_7116+245insTTTT	XP_011508219.1:n.7116+244_7116+245insTTTT
NM_003126.4:c.7134+244_7134+245insTTTT MANE Select	NP_003117.2:n.7134+244_7134+245insTTTT