Canonical Allele Identifier: CA2733101791

Linked Data

dbSNP Id: rs2151293335

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.90040290_90040291del , CM000678.2:g.90040290_90040291del GRCh38
NC_000016.9:g.90106698_90106699del , CM000678.1:g.90106698_90106699del GRCh37
NC_000016.8:g.88634199_88634200del NCBI36
NG_046598.1:g.25662_25663del

Transcript Alleles

HGVS Amino-acid Change
ENST00000268699.9:c.1012-10_1012-9del (GAS8) MANE Select ENSP00000268699.4:n.1012-10_1012-9del
ENST00000536122.7:c.937-10_937-9del (GAS8) ENSP00000440977.1:n.937-10_937-9del
ENST00000268699.8:c.1012-10_1012-9del (GAS8) ENSP00000268699.4:n.1012-10_1012-9del
ENST00000409873.5:n.820_821del (URAHP)
ENST00000536122.5:c.937-10_937-9del (GAS8) ENSP00000440977.1:n.937-10_937-9del
ENST00000540721.5:n.983-10_983-9del (GAS8)
ENST00000564789.5:n.248_249del (GAS8)
ENST00000566266.5:c.*972-10_*972-9del (GAS8) ENSP00000454343.1:n.*972-10_*972-9del
ENST00000569399.1:n.647-10_647-9del (GAS8)
ENST00000569558.5:n.1815-10_1815-9del (GAS8)
ENST00000620723.4:c.763-10_763-9del (GAS8) ENSP00000482877.1:n.763-10_763-9del
NM_001286205.1:c.763-10_763-9del (GAS8) NP_001273134.1:n.763-10_763-9del
NM_001286208.1:c.436-10_436-9del (GAS8) NP_001273137.1:n.436-10_436-9del
NM_001286209.1:c.937-10_937-9del (GAS8) NP_001273138.1:n.937-10_937-9del
NM_001481.2:c.1012-10_1012-9del (GAS8) NP_001472.1:n.1012-10_1012-9del
NR_027335.2:n.820_821del (URAHP)
XM_005256304.3:c.937-10_937-9del (GAS8) XP_005256361.1:n.937-10_937-9del
XM_005256309.3:c.436-10_436-9del (GAS8) XP_005256366.1:n.436-10_436-9del
XM_006721175.2:c.763-10_763-9del (GAS8) XP_006721238.1:n.763-10_763-9del
XM_011522990.1:c.763-10_763-9del (GAS8) XP_011521292.1:n.763-10_763-9del
XM_011522991.1:c.763-10_763-9del (GAS8) XP_011521293.1:n.763-10_763-9del
XM_011522992.1:c.763-10_763-9del (GAS8) XP_011521294.1:n.763-10_763-9del
XM_005256309.4:c.436-10_436-9del (GAS8) XP_005256366.1:n.436-10_436-9del
XM_006721175.3:c.763-10_763-9del (GAS8) XP_006721238.1:n.763-10_763-9del
XM_011522990.2:c.763-10_763-9del (GAS8) XP_011521292.1:n.763-10_763-9del
XM_011522992.2:c.763-10_763-9del (GAS8) XP_011521294.1:n.763-10_763-9del
XM_017023122.1:c.763-10_763-9del (GAS8) XP_016878611.1:n.763-10_763-9del
XM_017023123.1:c.763-10_763-9del (GAS8) XP_016878612.1:n.763-10_763-9del
XM_017023124.1:c.436-10_436-9del (GAS8) XP_016878613.1:n.436-10_436-9del
XM_017023125.1:c.436-10_436-9del (GAS8) XP_016878614.1:n.436-10_436-9del
XM_024450228.1:c.937-10_937-9del (GAS8) XP_024305996.1:n.937-10_937-9del
NM_001481.3:c.1012-10_1012-9del (GAS8) MANE Select NP_001472.1:n.1012-10_1012-9del
NM_001286205.2:c.763-10_763-9del (GAS8) NP_001273134.1:n.763-10_763-9del
NM_001286208.2:c.436-10_436-9del (GAS8) NP_001273137.1:n.436-10_436-9del
NM_001286209.2:c.937-10_937-9del (GAS8) NP_001273138.1:n.937-10_937-9del