Canonical Allele Identifier: CA9791751

Gene: SYNDIG1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.24543323C>G , CM000682.2:g.24543323C>G	GRCh38
NC_000020.10:g.24523959C>G , CM000682.1:g.24523959C>G	GRCh37
NC_000020.9:g.24471959C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376862.4:c.226C>G MANE Select	ENSP00000366058.3:p.Pro76Ala
ENST00000376862.3:c.226C>G	ENSP00000366058.3:p.Pro76Ala
NM_024893.2:c.226C>G	NP_079169.1:p.Pro76Ala
XM_011529347.1:c.226C>G	XP_011527649.1:p.Pro76Ala
XM_011529348.1:c.226C>G	XP_011527650.1:p.Pro76Ala
XM_011529349.1:c.226C>G	XP_011527651.1:p.Pro76Ala
XM_011529350.1:c.226C>G	XP_011527652.1:p.Pro76Ala
XM_011529351.1:c.226C>G	XP_011527653.1:p.Pro76Ala
XM_011529352.1:c.226C>G	XP_011527654.1:p.Pro76Ala
XM_011529353.1:c.226C>G	XP_011527655.1:p.Pro76Ala
XM_011529354.1:c.226C>G	XP_011527656.1:p.Pro76Ala
XM_011529355.1:c.226C>G	XP_011527657.1:p.Pro76Ala
XM_011529356.1:c.226C>G	XP_011527658.1:p.Pro76Ala
XM_011529357.1:c.226C>G	XP_011527659.1:p.Pro76Ala
XM_011529358.1:c.226C>G	XP_011527660.1:p.Pro76Ala
XR_937144.1:n.434C>G
NM_001323606.1:c.226C>G	NP_001310535.1:p.Pro76Ala
NM_001323607.1:c.226C>G	NP_001310536.1:p.Pro76Ala
NR_147606.1:n.577C>G
XM_011529347.3:c.226C>G	XP_011527649.1:p.Pro76Ala
XM_011529348.3:c.226C>G	XP_011527650.1:p.Pro76Ala
XM_011529349.3:c.226C>G	XP_011527651.1:p.Pro76Ala
XM_011529352.2:c.226C>G	XP_011527654.1:p.Pro76Ala
XM_011529353.2:c.226C>G	XP_011527655.1:p.Pro76Ala
XM_011529354.2:c.226C>G	XP_011527656.1:p.Pro76Ala
XM_011529356.3:c.226C>G	XP_011527658.1:p.Pro76Ala
XM_011529358.3:c.226C>G	XP_011527660.1:p.Pro76Ala
XM_017028064.1:c.226C>G	XP_016883553.1:p.Pro76Ala
XM_017028065.1:c.226C>G	XP_016883554.1:p.Pro76Ala
XM_017028066.2:c.226C>G	XP_016883555.1:p.Pro76Ala
XM_017028067.2:c.226C>G	XP_016883556.1:p.Pro76Ala
XM_017028068.1:c.226C>G	XP_016883557.1:p.Pro76Ala
XM_017028069.2:c.226C>G	XP_016883558.1:p.Pro76Ala
XR_937144.3:n.429C>G
NM_024893.3:c.226C>G MANE Select	NP_079169.1:p.Pro76Ala
NM_001323606.2:c.226C>G	NP_001310535.1:p.Pro76Ala
NM_001323607.2:c.226C>G	NP_001310536.1:p.Pro76Ala
NR_147606.2:n.665C>G