Canonical Allele Identifier: CA497196381

Linked Data

MyVariant Identifiers: chr16:g.90106779G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.90040371G>T , CM000678.2:g.90040371G>T GRCh38
NC_000016.9:g.90106779G>T , CM000678.1:g.90106779G>T GRCh37
NC_000016.8:g.88634280G>T NCBI36
NG_046598.1:g.25743G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000268699.9:c.1083G>T (GAS8) MANE Select ENSP00000268699.4:p.Gly361=
ENST00000536122.7:c.1008G>T (GAS8) ENSP00000440977.1:p.Gly336=
ENST00000268699.8:c.1083G>T (GAS8) ENSP00000268699.4:p.Gly361=
ENST00000409873.5:n.739C>A (URAHP)
ENST00000536122.5:c.1008G>T (GAS8) ENSP00000440977.1:p.Gly336=
ENST00000540721.5:n.1054G>T (GAS8)
ENST00000564789.5:n.329G>T (GAS8)
ENST00000566266.5:c.*1043G>T (GAS8) ENSP00000454343.1:n.*1043G>T
ENST00000569399.1:n.718G>T (GAS8)
ENST00000569558.5:n.1886G>T (GAS8)
ENST00000620723.4:c.834G>T (GAS8) ENSP00000482877.1:p.Gly278=
NM_001286205.1:c.834G>T (GAS8) NP_001273134.1:p.Gly278=
NM_001286208.1:c.507G>T (GAS8) NP_001273137.1:p.Gly169=
NM_001286209.1:c.1008G>T (GAS8) NP_001273138.1:p.Gly336=
NM_001481.2:c.1083G>T (GAS8) NP_001472.1:p.Gly361=
NR_027335.2:n.739C>A (URAHP)
XM_005256304.3:c.1008G>T (GAS8) XP_005256361.1:p.Gly336=
XM_005256309.3:c.507G>T (GAS8) XP_005256366.1:p.Gly169=
XM_006721175.2:c.834G>T (GAS8) XP_006721238.1:p.Gly278=
XM_011522990.1:c.834G>T (GAS8) XP_011521292.1:p.Gly278=
XM_011522991.1:c.834G>T (GAS8) XP_011521293.1:p.Gly278=
XM_011522992.1:c.834G>T (GAS8) XP_011521294.1:p.Gly278=
XM_005256309.4:c.507G>T (GAS8) XP_005256366.1:p.Gly169=
XM_006721175.3:c.834G>T (GAS8) XP_006721238.1:p.Gly278=
XM_011522990.2:c.834G>T (GAS8) XP_011521292.1:p.Gly278=
XM_011522992.2:c.834G>T (GAS8) XP_011521294.1:p.Gly278=
XM_017023122.1:c.834G>T (GAS8) XP_016878611.1:p.Gly278=
XM_017023123.1:c.834G>T (GAS8) XP_016878612.1:p.Gly278=
XM_017023124.1:c.507G>T (GAS8) XP_016878613.1:p.Gly169=
XM_017023125.1:c.507G>T (GAS8) XP_016878614.1:p.Gly169=
XM_024450228.1:c.1008G>T (GAS8) XP_024305996.1:p.Gly336=
NM_001481.3:c.1083G>T (GAS8) MANE Select NP_001472.1:p.Gly361=
NM_001286205.2:c.834G>T (GAS8) NP_001273134.1:p.Gly278=
NM_001286208.2:c.507G>T (GAS8) NP_001273137.1:p.Gly169=
NM_001286209.2:c.1008G>T (GAS8) NP_001273138.1:p.Gly336=