Canonical Allele Identifier: CA1821269862

Gene: ST3GAL1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133475643C= , CM000670.2:g.133475643C=	GRCh38
NC_000008.10:g.134487886C= , CM000670.1:g.134487886C=	GRCh37
NC_000008.9:g.134557068C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000522652.6:c.306+76G= MANE Select	ENSP00000430515.1:n.306+76G=
ENST00000648219.1:c.306+76G=	ENSP00000497381.1:n.306+76G=
ENST00000399640.3:c.306+76G=	ENSP00000414073.1:n.306+76G=
ENST00000517668.5:c.-84-9553G=	ENSP00000427720.1:n.-84-9553G=
ENST00000521180.5:c.306+76G=	ENSP00000428540.1:n.306+76G=
ENST00000522204.1:n.216+76G=
ENST00000522652.5:c.306+76G=	ENSP00000430515.1:n.306+76G=
ENST00000523854.5:c.-84-9553G=	ENSP00000429638.1:n.-84-9553G=
NM_003033.3:c.306+76G=	NP_003024.1:n.306+76G=
NM_173344.2:c.306+76G=	NP_775479.1:n.306+76G=
XM_005251023.1:c.306+76G=	XP_005251080.1:n.306+76G=
XM_005251024.3:c.306+76G=	XP_005251081.1:n.306+76G=
XM_005251025.3:c.306+76G=	XP_005251082.1:n.306+76G=
XM_006716617.1:c.306+76G=	XP_006716680.1:n.306+76G=
XM_011517225.1:c.306+76G=	XP_011515527.1:n.306+76G=
XM_011517226.1:c.306+76G=	XP_011515528.1:n.306+76G=
XM_005251025.5:c.306+76G=	XP_005251082.1:n.306+76G=
XM_006716617.2:c.306+76G=	XP_006716680.1:n.306+76G=
XM_011517225.2:c.306+76G=	XP_011515527.1:n.306+76G=
XM_017013736.2:c.306+76G=	XP_016869225.1:n.306+76G=
XM_024447233.1:c.306+76G=	XP_024303001.1:n.306+76G=
NM_173344.3:c.306+76G= MANE Select	NP_775479.1:n.306+76G=
NM_003033.4:c.306+76G=	NP_003024.1:n.306+76G=