Canonical Allele Identifier: CA397101082
Gene: GALNS HGNC NCBI
TRAPPC2L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88856777A>C , CM000678.2:g.88856777A>C GRCh38
NC_000016.9:g.88923185A>C , CM000678.1:g.88923185A>C GRCh37
NC_000016.8:g.87450686A>C NCBI36
NG_008667.1:g.5190T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000268695.10:c.101T>G (GALNS) MANE Select ENSP00000268695.5:p.Leu34Arg
ENST00000268695.9:c.101T>G (GALNS) ENSP00000268695.5:p.Leu34Arg
ENST00000564365.5:c.-398+531A>C (TRAPPC2L) ENSP00000455447.1:n.-398+531A>C
ENST00000565364.1:n.66T>G (GALNS)
ENST00000567525.5:c.50T>G (GALNS) ENSP00000454484.1:p.Leu17Arg
ENST00000568311.1:c.101T>G (GALNS) ENSP00000455006.1:p.Leu34Arg
ENST00000568613.5:c.50T>G (GALNS) ENSP00000457921.1:p.Leu17Arg
ENST00000569433.1:c.101T>G (GALNS) ENSP00000456884.1:p.Leu34Arg
NM_000512.4:c.101T>G (GALNS) NP_000503.1:p.Leu34Arg
XM_005256301.2:c.101T>G (GALNS) XP_005256358.1:p.Leu34Arg
XM_005256302.1:c.-52T>G (GALNS) XP_005256359.1:n.-52T>G
XM_011522982.1:c.-52T>G (GALNS) XP_011521284.1:n.-52T>G
XM_011522984.1:c.-52T>G (GALNS) XP_011521286.1:n.-52T>G
NM_001323543.1:c.-331T>G (GALNS) NP_001310472.1:n.-331T>G
NM_001323544.1:c.-52T>G (GALNS) NP_001310473.1:n.-52T>G
NR_134671.1:n.27+531A>C (TRAPPC2L)
XM_005256301.3:c.101T>G (GALNS) XP_005256358.1:p.Leu34Arg
XM_011522982.2:c.-52T>G (GALNS) XP_011521284.1:n.-52T>G
XM_017023113.1:c.-331T>G (GALNS) XP_016878602.1:n.-331T>G
NM_000512.5:c.101T>G (GALNS) MANE Select NP_000503.1:p.Leu34Arg
NM_001323543.2:c.-331T>G (GALNS) NP_001310472.1:n.-331T>G
NM_001323544.2:c.-52T>G (GALNS) NP_001310473.1:n.-52T>G
NR_134671.2:n.27+531A>C (TRAPPC2L)