Canonical Allele Identifier: CA2697334391

Gene: SPTA1

Linked Data

• dbSNP Id: rs2101744766

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158612800del , CM000663.2:g.158612800del	GRCh38
NC_000001.10:g.158582590del , CM000663.1:g.158582590del	GRCh37
NC_000001.9:g.156849214del	NCBI36
NG_011474.1:g.78918del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.7134+18del MANE Select	ENSP00000495214.1:n.7134+18del
ENST00000368147.8:c.7134+18del	ENSP00000357129.4:n.7134+18del
ENST00000481212.5:n.593del
ENST00000498708.1:n.584del
ENST00000614909.4:c.7134+18del	ENSP00000482595.1:n.7134+18del
NM_003126.2:c.7134+18del	NP_003117.2:n.7134+18del
XM_011509916.1:c.7134+18del	XP_011508218.1:n.7134+18del
XM_011509917.1:c.7116+18del	XP_011508219.1:n.7116+18del
NM_003126.3:c.7134+18del	NP_003117.2:n.7134+18del
XM_011509916.2:c.7134+18del	XP_011508218.1:n.7134+18del
XM_011509917.3:c.7116+18del	XP_011508219.1:n.7116+18del
NM_003126.4:c.7134+18del MANE Select	NP_003117.2:n.7134+18del