Canonical Allele Identifier: CA2733027140
Gene: GALNS HGNC NCBI

Linked Data

dbSNP Id: rs2143001656

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88836131A>C , CM000678.2:g.88836131A>C GRCh38
NC_000016.9:g.88902539A>C , CM000678.1:g.88902539A>C GRCh37
NC_000016.8:g.87430040A>C NCBI36
NG_008667.1:g.25836T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000268695.10:c.633+70T>G MANE Select ENSP00000268695.5:n.633+70T>G
ENST00000268695.9:c.633+70T>G ENSP00000268695.5:n.633+70T>G
ENST00000562593.5:n.4042+70T>G
ENST00000562831.1:c.417+70T>G ENSP00000455174.1:n.417+70T>G
ENST00000562931.5:n.221+70T>G
ENST00000566563.1:n.335+70T>G
ENST00000567525.5:c.314+70T>G ENSP00000454484.1:n.314+70T>G
ENST00000568613.5:c.752+70T>G ENSP00000457921.1:n.752+70T>G
NM_000512.4:c.633+70T>G NP_000503.1:n.633+70T>G
XM_005256301.2:c.633+70T>G XP_005256358.1:n.633+70T>G
XM_005256302.1:c.651+70T>G XP_005256359.1:n.651+70T>G
XM_011522982.1:c.651+70T>G XP_011521284.1:n.651+70T>G
XM_011522984.1:c.651+70T>G XP_011521286.1:n.651+70T>G
NM_001323543.1:c.78+70T>G NP_001310472.1:n.78+70T>G
NM_001323544.1:c.651+70T>G NP_001310473.1:n.651+70T>G
XM_005256301.3:c.633+70T>G XP_005256358.1:n.633+70T>G
XM_011522982.2:c.651+70T>G XP_011521284.1:n.651+70T>G
XM_017023111.2:c.651+70T>G XP_016878600.1:n.651+70T>G
XM_017023112.2:c.651+70T>G XP_016878601.1:n.651+70T>G
XM_017023113.1:c.78+70T>G XP_016878602.1:n.78+70T>G
NM_000512.5:c.633+70T>G MANE Select NP_000503.1:n.633+70T>G
NM_001323543.2:c.78+70T>G NP_001310472.1:n.78+70T>G
NM_001323544.2:c.651+70T>G NP_001310473.1:n.651+70T>G