Canonical Allele Identifier: CA371803229

Gene: SPAG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.100187244G>A , CM000670.2:g.100187244G>A	GRCh38
NC_000008.10:g.101199472G>A , CM000670.1:g.101199472G>A	GRCh37
NC_000008.9:g.101268648G>A	NCBI36
NG_033834.1:g.34210G>A
NG_033834.2:g.34210G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003114.5:c.826G>A MANE Select	NP_003105.2:p.Val276Ile
ENST00000388798.7:c.826G>A MANE Select	ENSP00000373450.3:p.Val276Ile
NM_001374321.1:c.826G>A	NP_001361250.1:p.Val276Ile
NM_003114.4:c.826G>A	NP_003105.2:p.Val276Ile
NM_172218.2:c.826G>A	NP_757367.1:p.Val276Ile
NM_172218.3:c.826G>A	NP_757367.1:p.Val276Ile
ENST00000251809.4:c.826G>A	ENSP00000251809.3:p.Val276Ile
ENST00000388798.6:c.826G>A	ENSP00000373450.2:p.Val276Ile
ENST00000520508.5:c.826G>A	ENSP00000428070.1:p.Val276Ile
ENST00000520643.5:c.826G>A	ENSP00000427716.1:p.Val276Ile
XM_011517240.1:c.826G>A	XP_011515542.1:p.Val276Ile
XM_011517240.2:c.826G>A	XP_011515542.1:p.Val276Ile
XM_011517241.1:c.826G>A	XP_011515543.1:p.Val276Ile
XM_011517241.2:c.826G>A	XP_011515543.1:p.Val276Ile
XM_011517242.1:c.826G>A	XP_011515544.1:p.Val276Ile
XM_011517242.2:c.826G>A	XP_011515544.1:p.Val276Ile
XM_011517243.1:c.826G>A	XP_011515545.1:p.Val276Ile
XM_011517243.2:c.826G>A	XP_011515545.1:p.Val276Ile
XM_011517244.1:c.826G>A	XP_011515546.1:p.Val276Ile
XM_011517245.1:c.826G>A	XP_011515547.1:p.Val276Ile
XM_011517245.2:c.826G>A	XP_011515547.1:p.Val276Ile
XM_017013754.1:c.931G>A	XP_016869243.1:p.Val311Ile
XM_017013755.1:c.490G>A	XP_016869244.1:p.Val164Ile
XR_001745580.1:n.912G>A
XR_001745581.1:n.912G>A
XR_001745582.1:n.912G>A
XR_001745583.1:n.912G>A