Canonical Allele Identifier: CA2634898038
Gene: GALNS HGNC NCBI
TRAPPC2L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88856543_88856544insGCTGAG , CM000678.2:g.88856543_88856544insGCTGAG GRCh38
NC_000016.9:g.88922951_88922952insGCTGAG , CM000678.1:g.88922951_88922952insGCTGAG GRCh37
NC_000016.8:g.87450452_87450453insGCTGAG NCBI36
NG_008667.1:g.5423_5424insCTCAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000268695.10:c.120+214_120+215insCTCAGC (GALNS) MANE Select ENSP00000268695.5:n.120+214_120+215insCTCAGC
ENST00000268695.9:c.120+214_120+215insCTCAGC (GALNS) ENSP00000268695.5:n.120+214_120+215insCTCAGC
ENST00000562831.1:c.-66_-65insCTCAGC (GALNS) ENSP00000455174.1:n.-66_-65insCTCAGC
ENST00000564365.5:c.-398+297_-398+298insGCTGAG (TRAPPC2L) ENSP00000455447.1:n.-398+297_-398+298insGCTGAG
ENST00000565364.1:n.85+214_85+215insCTCAGC (GALNS)
ENST00000567525.5:c.69+214_69+215insCTCAGC (GALNS) ENSP00000454484.1:n.69+214_69+215insCTCAGC
ENST00000568311.1:c.120+214_120+215insCTCAGC (GALNS) ENSP00000455006.1:n.120+214_120+215insCTCAGC
ENST00000568613.5:c.69+214_69+215insCTCAGC (GALNS) ENSP00000457921.1:n.69+214_69+215insCTCAGC
ENST00000569433.1:c.120+214_120+215insCTCAGC (GALNS) ENSP00000456884.1:n.120+214_120+215insCTCAGC
NM_000512.4:c.120+214_120+215insCTCAGC (GALNS) NP_000503.1:n.120+214_120+215insCTCAGC
XM_005256301.2:c.120+214_120+215insCTCAGC (GALNS) XP_005256358.1:n.120+214_120+215insCTCAGC
XM_005256302.1:c.-33+214_-33+215insCTCAGC (GALNS) XP_005256359.1:n.-33+214_-33+215insCTCAGC
XM_011522982.1:c.-33+214_-33+215insCTCAGC (GALNS) XP_011521284.1:n.-33+214_-33+215insCTCAGC
XM_011522984.1:c.-33+214_-33+215insCTCAGC (GALNS) XP_011521286.1:n.-33+214_-33+215insCTCAGC
XR_933884.1:n.36_37insCTCAGC
NM_001323543.1:c.-312+214_-312+215insCTCAGC (GALNS) NP_001310472.1:n.-312+214_-312+215insCTCAGC
NM_001323544.1:c.-33+214_-33+215insCTCAGC (GALNS) NP_001310473.1:n.-33+214_-33+215insCTCAGC
NR_134671.1:n.27+297_27+298insGCTGAG (TRAPPC2L)
XM_005256301.3:c.120+214_120+215insCTCAGC (GALNS) XP_005256358.1:n.120+214_120+215insCTCAGC
XM_011522982.2:c.-33+214_-33+215insCTCAGC (GALNS) XP_011521284.1:n.-33+214_-33+215insCTCAGC
XM_017023113.1:c.-312+214_-312+215insCTCAGC (GALNS) XP_016878602.1:n.-312+214_-312+215insCTCAGC
XR_933884.2:n.38_39insCTCAGC
NM_000512.5:c.120+214_120+215insCTCAGC (GALNS) MANE Select NP_000503.1:n.120+214_120+215insCTCAGC
NM_001323543.2:c.-312+214_-312+215insCTCAGC (GALNS) NP_001310472.1:n.-312+214_-312+215insCTCAGC
NM_001323544.2:c.-33+214_-33+215insCTCAGC (GALNS) NP_001310473.1:n.-33+214_-33+215insCTCAGC
NR_134671.2:n.27+297_27+298insGCTGAG (TRAPPC2L)