Canonical Allele Identifier: CA583868090

Gene: SPAG1

Linked Data

• dbSNP Id: rs1457518916
• gnomAD v2: 8-101203903-A-G
• gnomAD v3: 8-100191675-A-G
• gnomAD v4: 8-100191675-A-G
• MyVariant Identifiers: chr8:g.101203903A>G (hg19) ; chr8:g.100191675A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.100191675A>G , CM000670.2:g.100191675A>G	GRCh38
NC_000008.10:g.101203903A>G , CM000670.1:g.101203903A>G	GRCh37
NC_000008.9:g.101273079A>G	NCBI36
NG_033834.1:g.38641A>G
NG_033834.2:g.38641A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388798.7:c.939+179A>G MANE Select	ENSP00000373450.3:n.939+179A>G
ENST00000251809.4:c.939+179A>G	ENSP00000251809.3:n.939+179A>G
ENST00000388798.6:c.939+179A>G	ENSP00000373450.2:n.939+179A>G
ENST00000520508.5:c.939+179A>G	ENSP00000428070.1:n.939+179A>G
ENST00000520643.5:c.939+179A>G	ENSP00000427716.1:n.939+179A>G
NM_003114.4:c.939+179A>G	NP_003105.2:n.939+179A>G
NM_172218.2:c.939+179A>G	NP_757367.1:n.939+179A>G
XM_011517240.1:c.939+179A>G	XP_011515542.1:n.939+179A>G
XM_011517241.1:c.939+179A>G	XP_011515543.1:n.939+179A>G
XM_011517242.1:c.939+179A>G	XP_011515544.1:n.939+179A>G
XM_011517243.1:c.939+179A>G	XP_011515545.1:n.939+179A>G
XM_011517244.1:c.939+179A>G	XP_011515546.1:n.939+179A>G
XM_011517245.1:c.939+179A>G	XP_011515547.1:n.939+179A>G
XM_011517240.2:c.939+179A>G	XP_011515542.1:n.939+179A>G
XM_011517241.2:c.939+179A>G	XP_011515543.1:n.939+179A>G
XM_011517242.2:c.939+179A>G	XP_011515544.1:n.939+179A>G
XM_011517243.2:c.939+179A>G	XP_011515545.1:n.939+179A>G
XM_011517245.2:c.939+179A>G	XP_011515547.1:n.939+179A>G
XM_017013754.1:c.1044+179A>G	XP_016869243.1:n.1044+179A>G
XM_017013755.1:c.603+179A>G	XP_016869244.1:n.603+179A>G
XR_001745580.1:n.1025+179A>G
XR_001745581.1:n.1025+179A>G
XR_001745582.1:n.1025+179A>G
XR_001745583.1:n.1025+179A>G
NM_001374321.1:c.939+179A>G	NP_001361250.1:n.939+179A>G
NM_003114.5:c.939+179A>G MANE Select	NP_003105.2:n.939+179A>G
NM_172218.3:c.939+179A>G	NP_757367.1:n.939+179A>G