Canonical Allele Identifier: CA2241324508
Gene: GALNS HGNC NCBI

Linked Data

dbSNP Id: rs1911986363

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88835202_88835216dup , CM000678.2:g.88835202_88835216dup GRCh38
NC_000016.9:g.88901610_88901624dup , CM000678.1:g.88901610_88901624dup GRCh37
NC_000016.8:g.87429111_87429125dup NCBI36
NG_008667.1:g.26752_26766dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000268695.10:c.896_898+12dup
ENST00000268695.9:c.896_898+12dup
ENST00000562593.5:n.4305_4307+12dup
ENST00000562931.5:n.484_486+12dup
ENST00000567525.5:c.577_579+12dup
ENST00000568613.5:c.1015_1017+12dup
NM_000512.4:c.896_898+12dup
XM_005256301.2:c.896_898+12dup
XM_005256302.1:c.914_916+12dup
XM_011522982.1:c.914_916+12dup
XM_011522984.1:c.914_916+12dup
NM_001323543.1:c.341_343+12dup
NM_001323544.1:c.914_916+12dup
XM_005256301.3:c.896_898+12dup
XM_011522982.2:c.914_916+12dup
XM_017023111.2:c.914_916+12dup
XM_017023112.2:c.914_916+12dup
XM_017023113.1:c.341_343+12dup
NM_000512.5:c.896_898+12dup
NM_001323543.2:c.341_343+12dup
NM_001323544.2:c.914_916+12dup