Canonical Allele Identifier: CA1008228954

Gene: SPTA1

Linked Data

• gnomAD v3: 1-158612557-G-GTA
• gnomAD v4: 1-158612557-G-GTA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158612557_158612558insTA , CM000663.2:g.158612557_158612558insTA	GRCh38
NC_000001.10:g.158582347_158582348insTA , CM000663.1:g.158582347_158582348insTA	GRCh37
NC_000001.9:g.156848971_156848972insTA	NCBI36
NG_011474.1:g.79159_79160insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.7134+259_7134+260insTA MANE Select	ENSP00000495214.1:n.7134+259_7134+260insTA
ENST00000368147.8:c.7134+259_7134+260insTA	ENSP00000357129.4:n.7134+259_7134+260insTA
ENST00000614909.4:c.7134+259_7134+260insTA	ENSP00000482595.1:n.7134+259_7134+260insTA
NM_003126.2:c.7134+259_7134+260insTA	NP_003117.2:n.7134+259_7134+260insTA
XM_011509916.1:c.7134+259_7134+260insTA	XP_011508218.1:n.7134+259_7134+260insTA
XM_011509917.1:c.7116+259_7116+260insTA	XP_011508219.1:n.7116+259_7116+260insTA
NM_003126.3:c.7134+259_7134+260insTA	NP_003117.2:n.7134+259_7134+260insTA
XM_011509916.2:c.7134+259_7134+260insTA	XP_011508218.1:n.7134+259_7134+260insTA
XM_011509917.3:c.7116+259_7116+260insTA	XP_011508219.1:n.7116+259_7116+260insTA
NM_003126.4:c.7134+259_7134+260insTA MANE Select	NP_003117.2:n.7134+259_7134+260insTA