Canonical Allele Identifier: CA13826947

Gene: SPATA13

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24221351G>A , CM000675.2:g.24221351G>A	GRCh38
NC_000013.10:g.24795489G>A , CM000675.1:g.24795489G>A	GRCh37
NC_000013.9:g.23693489G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382108.8:c.-111-1468G>A MANE Select	ENSP00000371542.3:n.-111-1468G>A
ENST00000382095.8:c.-222-28126G>A	ENSP00000371527.4:n.-222-28126G>A
ENST00000382108.7:c.-111-1468G>A	ENSP00000371542.3:n.-111-1468G>A
ENST00000382141.4:c.-111-1468G>A	ENSP00000371576.4:n.-111-1468G>A
ENST00000424834.6:c.-111-1468G>A	ENSP00000398560.2:n.-111-1468G>A
ENST00000466831.2:n.212-1468G>A
NM_001166271.2:c.-111-1468G>A	NP_001159743.1:n.-111-1468G>A
NM_001286792.1:c.76-1468G>A	NP_001273721.1:n.76-1468G>A
NM_153023.3:c.-222-28126G>A	NP_694568.1:n.-222-28126G>A
NM_001166271.3:c.-111-1468G>A MANE Select	NP_001159743.1:n.-111-1468G>A
NM_001286792.2:c.76-1468G>A	NP_001273721.1:n.76-1468G>A
NM_153023.4:c.-222-28126G>A	NP_694568.1:n.-222-28126G>A