Canonical Allele Identifier: CA2007095987

Gene: ST3GAL4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126413890C= , CM000673.2:g.126413890C=	GRCh38
NC_000011.9:g.126283785C= , CM000673.1:g.126283785C=	GRCh37
NC_000011.8:g.125788995C=	NCBI36
NG_053025.1:g.63246C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356132.9:c.979-71C=	ENSP00000348451.5:n.979-71C=
ENST00000444328.7:c.916-71C= MANE Select	ENSP00000394354.2:n.916-71C=
ENST00000676831.1:n.1111-71C=
ENST00000676867.1:c.*95-71C=	ENSP00000503991.1:n.*95-71C=
ENST00000677503.1:c.822-71C=	ENSP00000504548.1:n.822-71C=
ENST00000677721.1:c.*180-71C=	ENSP00000502908.1:n.*180-71C=
ENST00000678865.1:c.834-71C=	ENSP00000504245.1:n.834-71C=
ENST00000227495.10:c.904-71C=	ENSP00000227495.6:n.904-71C=
ENST00000356132.8:c.934-71C=	ENSP00000348451.4:n.934-71C=
ENST00000392669.6:c.916-71C=	ENSP00000376437.2:n.916-71C=
ENST00000444328.6:c.916-71C=	ENSP00000394354.2:n.916-71C=
ENST00000449406.6:c.883-71C=	ENSP00000399444.2:n.883-71C=
ENST00000524834.5:n.629+4479C=
ENST00000524860.1:c.424-71C=	ENSP00000431170.1:n.424-71C=
ENST00000526727.5:c.916-71C=	ENSP00000436047.1:n.916-71C=
ENST00000530591.5:c.904-71C=	ENSP00000433989.1:n.904-71C=
ENST00000531217.5:c.*474-71C=	ENSP00000432929.1:n.*474-71C=
ENST00000532243.5:c.913-71C=	ENSP00000434349.1:n.913-71C=
ENST00000533826.1:n.444-71C=
ENST00000534083.5:c.916-71C=	ENSP00000433318.1:n.916-71C=
ENST00000534457.5:c.901-71C=	ENSP00000434668.1:n.901-71C=
NM_001254757.1:c.916-71C=	NP_001241686.1:n.916-71C=
NM_001254758.1:c.916-71C=	NP_001241687.1:n.916-71C=
NM_001254759.1:c.913-71C=	NP_001241688.1:n.913-71C=
NM_006278.2:c.904-71C=	NP_006269.1:n.904-71C=
XM_011542959.1:c.771+4479C=	XP_011541261.1:n.771+4479C=
XM_011542960.1:c.771+4479C=	XP_011541262.1:n.771+4479C=
XM_011542961.1:c.771+4479C=	XP_011541263.1:n.771+4479C=
XM_011542962.1:c.771+4479C=	XP_011541264.1:n.771+4479C=
NM_001348396.1:c.979-71C=	NP_001335325.1:n.979-71C=
NM_001348397.1:c.979-71C=	NP_001335326.1:n.979-71C=
NM_001348398.1:c.822-71C=	NP_001335327.1:n.822-71C=
NM_001348399.1:c.916-71C=	NP_001335328.1:n.916-71C=
NM_001348400.1:c.904-71C=	NP_001335329.1:n.904-71C=
NR_145671.1:n.1349-71C=
XM_024448658.1:c.916-71C=	XP_024304426.1:n.916-71C=
XM_024448659.1:c.916-71C=	XP_024304427.1:n.916-71C=
XM_024448660.1:c.916-71C=	XP_024304428.1:n.916-71C=
NM_001254757.2:c.916-71C= MANE Select	NP_001241686.1:n.916-71C=
NM_001254759.2:c.913-71C=	NP_001241688.1:n.913-71C=
NM_001348396.2:c.979-71C=	NP_001335325.1:n.979-71C=
NM_001348397.2:c.979-71C=	NP_001335326.1:n.979-71C=
NM_001348398.2:c.822-71C=	NP_001335327.1:n.822-71C=
NM_001348399.2:c.916-71C=	NP_001335328.1:n.916-71C=
NM_001348400.2:c.904-71C=	NP_001335329.1:n.904-71C=
NM_006278.3:c.904-71C=	NP_006269.1:n.904-71C=
NR_145671.2:n.1308-71C=
NM_001254758.2:c.916-71C=	NP_001241687.1:n.916-71C=