Canonical Allele Identifier: CA2648555482

Gene: SPTA1

Linked Data

• gnomAD v4: 1-158612635-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158612635_158612636insA , CM000663.2:g.158612635_158612636insA	GRCh38
NC_000001.10:g.158582425_158582426insA , CM000663.1:g.158582425_158582426insA	GRCh37
NC_000001.9:g.156849049_156849050insA	NCBI36
NG_011474.1:g.79081_79082insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.7134+181_7134+182insT MANE Select	ENSP00000495214.1:n.7134+181_7134+182insT
ENST00000368147.8:c.7134+181_7134+182insT	ENSP00000357129.4:n.7134+181_7134+182insT
ENST00000614909.4:c.7134+181_7134+182insT	ENSP00000482595.1:n.7134+181_7134+182insT
NM_003126.2:c.7134+181_7134+182insT	NP_003117.2:n.7134+181_7134+182insT
XM_011509916.1:c.7134+181_7134+182insT	XP_011508218.1:n.7134+181_7134+182insT
XM_011509917.1:c.7116+181_7116+182insT	XP_011508219.1:n.7116+181_7116+182insT
NM_003126.3:c.7134+181_7134+182insT	NP_003117.2:n.7134+181_7134+182insT
XM_011509916.2:c.7134+181_7134+182insT	XP_011508218.1:n.7134+181_7134+182insT
XM_011509917.3:c.7116+181_7116+182insT	XP_011508219.1:n.7116+181_7116+182insT
NM_003126.4:c.7134+181_7134+182insT MANE Select	NP_003117.2:n.7134+181_7134+182insT