Canonical Allele Identifier: CA1427202127

Gene: ST6GAL1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.187008099G= , CM000665.2:g.187008099G=	GRCh38
NC_000003.11:g.186725887G= , CM000665.1:g.186725887G=	GRCh37
NC_000003.10:g.188208581G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_173216.2:c.-182-30643G= MANE Select	NP_775323.1:n.-182-30643G=
ENST00000169298.8:c.-182-30643G= MANE Select	ENSP00000169298.3:n.-182-30643G=
NM_173217.2:c.-218-30643G=	NP_775324.1:n.-218-30643G=
ENST00000169298.7:c.-182-30643G=	ENSP00000169298.3:n.-182-30643G=
ENST00000417392.5:c.-182-30643G=	ENSP00000407631.1:n.-182-30643G=
ENST00000427315.5:c.-86-43150G=	ENSP00000412821.1:n.-86-43150G=
ENST00000430309.5:c.-182-30643G=	ENSP00000399525.1:n.-182-30643G=
ENST00000438590.5:c.-182-30643G=	ENSP00000416163.1:n.-182-30643G=
ENST00000448408.5:c.-183+11426G=	ENSP00000390793.1:n.-183+11426G=
ENST00000455441.5:c.-86-43150G=	ENSP00000397273.1:n.-86-43150G=
ENST00000457772.6:c.-218-30643G=	ENSP00000412221.2:n.-218-30643G=
ENST00000458216.5:c.-232-30643G=	ENSP00000400547.1:n.-232-30643G=
ENST00000676633.1:c.-183+11426G=	ENSP00000504448.1:n.-183+11426G=
ENST00000676786.1:n.653-9485G=
ENST00000677292.1:c.-182-30643G=	ENSP00000503457.1:n.-182-30643G=
XM_005247717.2:c.-183+11426G=	XP_005247774.1:n.-183+11426G=
XM_006713734.1:c.-182-30643G=	XP_006713797.1:n.-182-30643G=
XM_011513085.1:c.-182-30643G=	XP_011511387.1:n.-182-30643G=
XM_011513086.1:c.-182-30643G=	XP_011511388.1:n.-182-30643G=
XR_924163.1:n.493-30643G=