Canonical Allele Identifier: CA397089100
Community Standard Title: NM_000512.5(GALNS):c.294C>G (p.Tyr98Ter)
Gene: GALNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88841922G>C , CM000678.2:g.88841922G>C GRCh38
NC_000016.9:g.88908330G>C , CM000678.1:g.88908330G>C GRCh37
NC_000016.8:g.87435831G>C NCBI36
NG_008667.1:g.20045C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000512.5:c.294C>G MANE Select NP_000503.1:p.Tyr98Ter
ENST00000268695.10:c.294C>G MANE Select ENSP00000268695.5:p.Tyr98Ter
NM_000512.4:c.294C>G NP_000503.1:p.Tyr98Ter
NM_001323543.1:c.-262C>G NP_001310472.1:n.-262C>G
NM_001323543.2:c.-262C>G NP_001310472.1:n.-262C>G
NM_001323544.1:c.312C>G NP_001310473.1:p.Tyr104Ter
NM_001323544.2:c.312C>G NP_001310473.1:p.Tyr104Ter
ENST00000268695.9:c.294C>G ENSP00000268695.5:p.Tyr98Ter
ENST00000562593.5:n.3703C>G
ENST00000562831.1:c.78C>G ENSP00000455174.1:p.Tyr26Ter
ENST00000565364.1:n.429C>G
ENST00000567525.5:c.119C>G ENSP00000454484.1:p.Thr40Arg
ENST00000567779.1:n.124C>G
ENST00000568613.5:c.413C>G ENSP00000457921.1:n.413C>G
XM_005256301.2:c.294C>G XP_005256358.1:p.Tyr98Ter
XM_005256301.3:c.294C>G XP_005256358.1:p.Tyr98Ter
XM_005256302.1:c.312C>G XP_005256359.1:p.Tyr104Ter
XM_011522982.1:c.312C>G XP_011521284.1:p.Tyr104Ter
XM_011522982.2:c.312C>G XP_011521284.1:p.Tyr104Ter
XM_011522984.1:c.312C>G XP_011521286.1:p.Tyr104Ter
XM_017023111.2:c.312C>G XP_016878600.1:p.Tyr104Ter
XM_017023112.2:c.312C>G XP_016878601.1:p.Tyr104Ter
XM_017023113.1:c.-262C>G XP_016878602.1:n.-262C>G