Canonical Allele Identifier: CA397101397
Gene: GALNS HGNC NCBI
TRAPPC2L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88856811C>T , CM000678.2:g.88856811C>T GRCh38
NC_000016.9:g.88923219C>T , CM000678.1:g.88923219C>T GRCh37
NC_000016.8:g.87450720C>T NCBI36
NG_008667.1:g.5156G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000268695.10:c.67G>A (GALNS) MANE Select ENSP00000268695.5:p.Gly23Arg
ENST00000268695.9:c.67G>A (GALNS) ENSP00000268695.5:p.Gly23Arg
ENST00000564365.5:c.-398+565C>T (TRAPPC2L) ENSP00000455447.1:n.-398+565C>T
ENST00000565364.1:n.32G>A (GALNS)
ENST00000567525.5:c.16G>A (GALNS) ENSP00000454484.1:p.Gly6Arg
ENST00000568311.1:c.67G>A (GALNS) ENSP00000455006.1:p.Gly23Arg
ENST00000568613.5:c.16G>A (GALNS) ENSP00000457921.1:p.Gly6Arg
ENST00000569433.1:c.67G>A (GALNS) ENSP00000456884.1:p.Gly23Arg
NM_000512.4:c.67G>A (GALNS) NP_000503.1:p.Gly23Arg
XM_005256301.2:c.67G>A (GALNS) XP_005256358.1:p.Gly23Arg
XM_005256302.1:c.-86G>A (GALNS) XP_005256359.1:n.-86G>A
XM_011522982.1:c.-86G>A (GALNS) XP_011521284.1:n.-86G>A
XM_011522984.1:c.-86G>A (GALNS) XP_011521286.1:n.-86G>A
NM_001323543.1:c.-365G>A (GALNS) NP_001310472.1:n.-365G>A
NM_001323544.1:c.-86G>A (GALNS) NP_001310473.1:n.-86G>A
NR_134671.1:n.27+565C>T (TRAPPC2L)
XM_005256301.3:c.67G>A (GALNS) XP_005256358.1:p.Gly23Arg
XM_011522982.2:c.-86G>A (GALNS) XP_011521284.1:n.-86G>A
XM_017023113.1:c.-365G>A (GALNS) XP_016878602.1:n.-365G>A
NM_000512.5:c.67G>A (GALNS) MANE Select NP_000503.1:p.Gly23Arg
NM_001323543.2:c.-365G>A (GALNS) NP_001310472.1:n.-365G>A
NM_001323544.2:c.-86G>A (GALNS) NP_001310473.1:n.-86G>A
NR_134671.2:n.27+565C>T (TRAPPC2L)