Canonical Allele Identifier: CA8257470

Gene: GAS8

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.90027735G>A , CM000678.2:g.90027735G>A	GRCh38
NC_000016.9:g.90094143G>A , CM000678.1:g.90094143G>A	GRCh37
NC_000016.8:g.88621644G>A	NCBI36
NG_046598.1:g.13107G>A
NG_054714.1:g.7167C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001481.3:c.90+13G>A MANE Select	NP_001472.1:n.90+13G>A
ENST00000268699.9:c.90+13G>A MANE Select	ENSP00000268699.4:n.90+13G>A
NM_001286205.1:c.-283+13G>A	NP_001273134.1:n.-283+13G>A
NM_001286205.2:c.-283+13G>A	NP_001273134.1:n.-283+13G>A
NM_001286208.1:c.-555+13G>A	NP_001273137.1:n.-555+13G>A
NM_001286208.2:c.-555+13G>A	NP_001273137.1:n.-555+13G>A
NM_001286209.1:c.15+13G>A	NP_001273138.1:n.15+13G>A
NM_001286209.2:c.15+13G>A	NP_001273138.1:n.15+13G>A
NM_001481.2:c.90+13G>A	NP_001472.1:n.90+13G>A
ENST00000268699.8:c.90+13G>A	ENSP00000268699.4:n.90+13G>A
ENST00000536122.5:c.15+13G>A	ENSP00000440977.1:n.15+13G>A
ENST00000536122.7:c.15+13G>A	ENSP00000440977.1:n.15+13G>A
ENST00000537797.5:n.129+13G>A
ENST00000540721.5:n.62-3564G>A
ENST00000561675.1:c.-268-3455G>A	ENSP00000457554.1:n.-268-3455G>A
ENST00000563936.5:c.15+13G>A	ENSP00000454905.1:n.15+13G>A
ENST00000563980.5:n.469+13G>A
ENST00000564392.5:c.15+13G>A	ENSP00000455172.1:n.15+13G>A
ENST00000564853.1:n.155G>A
ENST00000565062.5:c.90+13G>A	ENSP00000455936.1:n.90+13G>A
ENST00000565957.5:n.332+13G>A
ENST00000566266.5:c.90+13G>A	ENSP00000454343.1:n.90+13G>A
ENST00000568664.5:n.126+13G>A
ENST00000568705.5:n.163+13G>A
ENST00000620723.4:c.-283+13G>A	ENSP00000482877.1:n.-283+13G>A
XM_005256304.3:c.15+13G>A	XP_005256361.1:n.15+13G>A
XM_005256309.4:c.-802+13G>A	XP_005256366.1:n.-802+13G>A
XM_006721175.2:c.-269+13G>A	XP_006721238.1:n.-269+13G>A
XM_006721175.3:c.-269+13G>A	XP_006721238.1:n.-269+13G>A
XM_011522990.1:c.-283+13G>A	XP_011521292.1:n.-283+13G>A
XM_011522990.2:c.-283+13G>A	XP_011521292.1:n.-283+13G>A
XM_011522991.1:c.-269+13G>A	XP_011521293.1:n.-269+13G>A
XM_011522992.1:c.-268-3455G>A	XP_011521294.1:n.-268-3455G>A
XM_011522992.2:c.-268-3455G>A	XP_011521294.1:n.-268-3455G>A
XM_017023122.1:c.-283+13G>A	XP_016878611.1:n.-283+13G>A
XM_017023123.1:c.-283+13G>A	XP_016878612.1:n.-283+13G>A
XM_017023124.1:c.-432+13G>A	XP_016878613.1:n.-432+13G>A
XM_017023125.1:c.-541+13G>A	XP_016878614.1:n.-541+13G>A
XM_024450228.1:c.15+13G>A	XP_024305996.1:n.15+13G>A