Canonical Allele Identifier: CA11518879
Gene: ST6GAL1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.187005156G>A , CM000665.2:g.187005156G>A GRCh38
NC_000003.11:g.186722944G>A , CM000665.1:g.186722944G>A GRCh37
NC_000003.10:g.188205638G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000169298.8:c.-182-33586G>A MANE Select ENSP00000169298.3:n.-182-33586G>A
ENST00000676633.1:c.-183+8483G>A ENSP00000504448.1:n.-183+8483G>A
ENST00000676786.1:n.653-12428G>A
ENST00000677292.1:c.-182-33586G>A ENSP00000503457.1:n.-182-33586G>A
ENST00000169298.7:c.-182-33586G>A ENSP00000169298.3:n.-182-33586G>A
ENST00000417392.5:c.-182-33586G>A ENSP00000407631.1:n.-182-33586G>A
ENST00000427315.5:c.-86-46093G>A ENSP00000412821.1:n.-86-46093G>A
ENST00000430309.5:c.-182-33586G>A ENSP00000399525.1:n.-182-33586G>A
ENST00000438590.5:c.-183+30066G>A ENSP00000416163.1:n.-183+30066G>A
ENST00000448408.5:c.-183+8483G>A ENSP00000390793.1:n.-183+8483G>A
ENST00000455441.5:c.-87+41230G>A ENSP00000397273.1:n.-87+41230G>A
ENST00000457772.6:c.-218-33586G>A ENSP00000412221.2:n.-218-33586G>A
ENST00000458216.5:c.-232-33586G>A ENSP00000400547.1:n.-232-33586G>A
ENST00000485105.1:n.53-986G>A
NM_173216.2:c.-182-33586G>A MANE Select NP_775323.1:n.-182-33586G>A
NM_173217.2:c.-218-33586G>A NP_775324.1:n.-218-33586G>A
XM_005247717.2:c.-183+8483G>A XP_005247774.1:n.-183+8483G>A
XM_006713734.1:c.-182-33586G>A XP_006713797.1:n.-182-33586G>A
XM_011513085.1:c.-182-33586G>A XP_011511387.1:n.-182-33586G>A
XM_011513086.1:c.-183+30066G>A XP_011511388.1:n.-183+30066G>A
XR_924163.1:n.493-33586G>A
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