Canonical Allele Identifier: CA980347281
Gene: GALNS HGNC NCBI
TRAPPC2L HGNC NCBI

Linked Data

dbSNP Id: rs1337481994

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88856552G>T , CM000678.2:g.88856552G>T GRCh38
NC_000016.9:g.88922960G>T , CM000678.1:g.88922960G>T GRCh37
NC_000016.8:g.87450461G>T NCBI36
NG_008667.1:g.5415C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000268695.10:c.120+206C>A (GALNS) MANE Select ENSP00000268695.5:n.120+206C>A
ENST00000268695.9:c.120+206C>A (GALNS) ENSP00000268695.5:n.120+206C>A
ENST00000562831.1:c.-74C>A (GALNS) ENSP00000455174.1:n.-74C>A
ENST00000564365.5:c.-398+306G>T (TRAPPC2L) ENSP00000455447.1:n.-398+306G>T
ENST00000565364.1:n.85+206C>A (GALNS)
ENST00000567525.5:c.69+206C>A (GALNS) ENSP00000454484.1:n.69+206C>A
ENST00000568311.1:c.120+206C>A (GALNS) ENSP00000455006.1:n.120+206C>A
ENST00000568613.5:c.69+206C>A (GALNS) ENSP00000457921.1:n.69+206C>A
ENST00000569433.1:c.120+206C>A (GALNS) ENSP00000456884.1:n.120+206C>A
NM_000512.4:c.120+206C>A (GALNS) NP_000503.1:n.120+206C>A
XM_005256301.2:c.120+206C>A (GALNS) XP_005256358.1:n.120+206C>A
XM_005256302.1:c.-33+206C>A (GALNS) XP_005256359.1:n.-33+206C>A
XM_011522982.1:c.-33+206C>A (GALNS) XP_011521284.1:n.-33+206C>A
XM_011522984.1:c.-33+206C>A (GALNS) XP_011521286.1:n.-33+206C>A
XR_933884.1:n.28C>A
NM_001323543.1:c.-312+206C>A (GALNS) NP_001310472.1:n.-312+206C>A
NM_001323544.1:c.-33+206C>A (GALNS) NP_001310473.1:n.-33+206C>A
NR_134671.1:n.27+306G>T (TRAPPC2L)
XM_005256301.3:c.120+206C>A (GALNS) XP_005256358.1:n.120+206C>A
XM_011522982.2:c.-33+206C>A (GALNS) XP_011521284.1:n.-33+206C>A
XM_017023113.1:c.-312+206C>A (GALNS) XP_016878602.1:n.-312+206C>A
XR_933884.2:n.30C>A
NM_000512.5:c.120+206C>A (GALNS) MANE Select NP_000503.1:n.120+206C>A
NM_001323543.2:c.-312+206C>A (GALNS) NP_001310472.1:n.-312+206C>A
NM_001323544.2:c.-33+206C>A (GALNS) NP_001310473.1:n.-33+206C>A
NR_134671.2:n.27+306G>T (TRAPPC2L)