Canonical Allele Identifier: CA182382728

Gene: SPAG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.100212989A>G , CM000670.2:g.100212989A>G	GRCh38
NC_000008.10:g.101225217A>G , CM000670.1:g.101225217A>G	GRCh37
NC_000008.9:g.101294393A>G	NCBI36
NG_033834.1:g.59955A>G
NG_033834.2:g.59955A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_003114.5:c.1097-101A>G MANE Select	NP_003105.2:n.1097-101A>G
ENST00000388798.7:c.1097-101A>G MANE Select	ENSP00000373450.3:n.1097-101A>G
NM_001374321.1:c.1097-101A>G	NP_001361250.1:n.1097-101A>G
NM_003114.4:c.1097-101A>G	NP_003105.2:n.1097-101A>G
NM_172218.2:c.1097-101A>G	NP_757367.1:n.1097-101A>G
NM_172218.3:c.1097-101A>G	NP_757367.1:n.1097-101A>G
ENST00000251809.4:c.1097-101A>G	ENSP00000251809.3:n.1097-101A>G
ENST00000388798.6:c.1097-101A>G	ENSP00000373450.2:n.1097-101A>G
XM_011517240.1:c.1097-101A>G	XP_011515542.1:n.1097-101A>G
XM_011517240.2:c.1097-101A>G	XP_011515542.1:n.1097-101A>G
XM_011517241.1:c.1097-101A>G	XP_011515543.1:n.1097-101A>G
XM_011517241.2:c.1097-101A>G	XP_011515543.1:n.1097-101A>G
XM_011517242.1:c.1097-101A>G	XP_011515544.1:n.1097-101A>G
XM_011517242.2:c.1097-101A>G	XP_011515544.1:n.1097-101A>G
XM_011517243.1:c.1097-101A>G	XP_011515545.1:n.1097-101A>G
XM_011517243.2:c.1097-101A>G	XP_011515545.1:n.1097-101A>G
XM_011517244.1:c.1097-101A>G	XP_011515546.1:n.1097-101A>G
XM_011517245.1:c.1097-101A>G	XP_011515547.1:n.1097-101A>G
XM_011517245.2:c.1097-101A>G	XP_011515547.1:n.1097-101A>G
XM_017013754.1:c.1202-101A>G	XP_016869243.1:n.1202-101A>G
XM_017013755.1:c.761-101A>G	XP_016869244.1:n.761-101A>G
XR_001745580.1:n.1183-101A>G
XR_001745581.1:n.1183-101A>G
XR_001745582.1:n.1183-101A>G
XR_001745583.1:n.1183-101A>G