Canonical Allele Identifier: CA2241338049

Gene: GALNS TRAPPC2L

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88856718_88856739delinsCCCCACCCCGGCCCTGCCCCGT , CM000678.2:g.88856718_88856739delinsCCCCACCCCGGCCCTGCCCCGT	GRCh38
NC_000016.9:g.88923126_88923147delinsCCCCACCCCGGCCCTGCCCCGT , CM000678.1:g.88923126_88923147delinsCCCCACCCCGGCCCTGCCCCGT	GRCh37
NC_000016.8:g.87450627_87450648delinsCCCCACCCCGGCCCTGCCCCGT	NCBI36
NG_008667.1:g.5228_5249delinsACGGGGCAGGGCCGGGGTGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268695.10:c.120+19_120+40delinsACGGGGCAGGGCCGGGGTGGGG (GALNS) MANE Select	ENSP00000268695.5:n.120+19_120+40delinsACGGGGCAGGGCCGGGGTGGGG...
ENST00000268695.9:c.120+19_120+40delinsACGGGGCAGGGCCGGGGTGGGG (GALNS)	ENSP00000268695.5:n.120+19_120+40delinsACGGGGCAGGGCCGGGGTGGGG...
ENST00000564365.5:c.-398+472_-398+493delinsCCCCACCCCGGCCCTGCCCCGT (TRAPPC2L)	ENSP00000455447.1:n.-398+472_-398+493delinsCCCCACCCCGGCCCTGCC...
ENST00000565364.1:n.85+19_85+40delinsACGGGGCAGGGCCGGGGTGGGG (GALNS)
ENST00000567525.5:c.69+19_69+40delinsACGGGGCAGGGCCGGGGTGGGG (GALNS)	ENSP00000454484.1:n.69+19_69+40delinsACGGGGCAGGGCCGGGGTGGGG
ENST00000568311.1:c.120+19_120+40delinsACGGGGCAGGGCCGGGGTGGGG (GALNS)	ENSP00000455006.1:n.120+19_120+40delinsACGGGGCAGGGCCGGGGTGGGG...
ENST00000568613.5:c.69+19_69+40delinsACGGGGCAGGGCCGGGGTGGGG (GALNS)	ENSP00000457921.1:n.69+19_69+40delinsACGGGGCAGGGCCGGGGTGGGG
ENST00000569433.1:c.120+19_120+40delinsACGGGGCAGGGCCGGGGTGGGG (GALNS)	ENSP00000456884.1:n.120+19_120+40delinsACGGGGCAGGGCCGGGGTGGGG...
NM_000512.4:c.120+19_120+40delinsACGGGGCAGGGCCGGGGTGGGG (GALNS)	NP_000503.1:n.120+19_120+40delinsACGGGGCAGGGCCGGGGTGGGG
XM_005256301.2:c.120+19_120+40delinsACGGGGCAGGGCCGGGGTGGGG (GALNS)	XP_005256358.1:n.120+19_120+40delinsACGGGGCAGGGCCGGGGTGGGG
XM_005256302.1:c.-33+19_-33+40delinsACGGGGCAGGGCCGGGGTGGGG (GALNS)	XP_005256359.1:n.-33+19_-33+40delinsACGGGGCAGGGCCGGGGTGGGG
XM_011522982.1:c.-33+19_-33+40delinsACGGGGCAGGGCCGGGGTGGGG (GALNS)	XP_011521284.1:n.-33+19_-33+40delinsACGGGGCAGGGCCGGGGTGGGG
XM_011522984.1:c.-33+19_-33+40delinsACGGGGCAGGGCCGGGGTGGGG (GALNS)	XP_011521286.1:n.-33+19_-33+40delinsACGGGGCAGGGCCGGGGTGGGG
NM_001323543.1:c.-312+19_-312+40delinsACGGGGCAGGGCCGGGGTGGGG (GALNS)	NP_001310472.1:n.-312+19_-312+40delinsACGGGGCAGGGCCGGGGTGGGG
NM_001323544.1:c.-33+19_-33+40delinsACGGGGCAGGGCCGGGGTGGGG (GALNS)	NP_001310473.1:n.-33+19_-33+40delinsACGGGGCAGGGCCGGGGTGGGG
NR_134671.1:n.27+472_27+493delinsCCCCACCCCGGCCCTGCCCCGT (TRAPPC2L)
XM_005256301.3:c.120+19_120+40delinsACGGGGCAGGGCCGGGGTGGGG (GALNS)	XP_005256358.1:n.120+19_120+40delinsACGGGGCAGGGCCGGGGTGGGG
XM_011522982.2:c.-33+19_-33+40delinsACGGGGCAGGGCCGGGGTGGGG (GALNS)	XP_011521284.1:n.-33+19_-33+40delinsACGGGGCAGGGCCGGGGTGGGG
XM_017023113.1:c.-312+19_-312+40delinsACGGGGCAGGGCCGGGGTGGGG (GALNS)	XP_016878602.1:n.-312+19_-312+40delinsACGGGGCAGGGCCGGGGTGGGG
NM_000512.5:c.120+19_120+40delinsACGGGGCAGGGCCGGGGTGGGG (GALNS) MANE Select	NP_000503.1:n.120+19_120+40delinsACGGGGCAGGGCCGGGGTGGGG
NM_001323543.2:c.-312+19_-312+40delinsACGGGGCAGGGCCGGGGTGGGG (GALNS)	NP_001310472.1:n.-312+19_-312+40delinsACGGGGCAGGGCCGGGGTGGGG
NM_001323544.2:c.-33+19_-33+40delinsACGGGGCAGGGCCGGGGTGGGG (GALNS)	NP_001310473.1:n.-33+19_-33+40delinsACGGGGCAGGGCCGGGGTGGGG
NR_134671.2:n.27+472_27+493delinsCCCCACCCCGGCCCTGCCCCGT (TRAPPC2L)