Canonical Allele Identifier: CA673064909

Gene: ST3GAL4

Linked Data

• dbSNP Id: rs1405351000
• gnomAD v3: 11-126411986-T-C
• gnomAD v4: 11-126411986-T-C
• MyVariant Identifiers: chr11:g.126281881T>C (hg19) ; chr11:g.126411986T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126411986T>C , CM000673.2:g.126411986T>C	GRCh38
NC_000011.9:g.126281881T>C , CM000673.1:g.126281881T>C	GRCh37
NC_000011.8:g.125787091T>C	NCBI36
NG_053025.1:g.61342T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356132.9:c.835-1519T>C	ENSP00000348451.5:n.835-1519T>C
ENST00000444328.7:c.772-1519T>C MANE Select	ENSP00000394354.2:n.772-1519T>C
ENST00000676831.1:n.967-1519T>C
ENST00000676867.1:c.772-1344T>C	ENSP00000503991.1:n.772-1344T>C
ENST00000677503.1:c.760-1601T>C	ENSP00000504548.1:n.760-1601T>C
ENST00000677721.1:c.*36-1519T>C	ENSP00000502908.1:n.*36-1519T>C
ENST00000678865.1:c.772-1601T>C	ENSP00000504245.1:n.772-1601T>C
ENST00000227495.10:c.760-1519T>C	ENSP00000227495.6:n.760-1519T>C
ENST00000356132.8:c.790-1519T>C	ENSP00000348451.4:n.790-1519T>C
ENST00000392669.6:c.772-1519T>C	ENSP00000376437.2:n.772-1519T>C
ENST00000444328.6:c.772-1519T>C	ENSP00000394354.2:n.772-1519T>C
ENST00000449406.6:c.739-1519T>C	ENSP00000399444.2:n.739-1519T>C
ENST00000524834.5:n.629+2575T>C
ENST00000524860.1:c.280-1519T>C	ENSP00000431170.1:n.280-1519T>C
ENST00000526727.5:c.772-1519T>C	ENSP00000436047.1:n.772-1519T>C
ENST00000530591.5:c.760-1519T>C	ENSP00000433989.1:n.760-1519T>C
ENST00000531217.5:c.*330-1519T>C	ENSP00000432929.1:n.*330-1519T>C
ENST00000532243.5:c.769-1519T>C	ENSP00000434349.1:n.769-1519T>C
ENST00000533826.1:n.192-1411T>C
ENST00000534083.5:c.772-1519T>C	ENSP00000433318.1:n.772-1519T>C
ENST00000534457.5:c.757-1519T>C	ENSP00000434668.1:n.757-1519T>C
NM_001254757.1:c.772-1519T>C	NP_001241686.1:n.772-1519T>C
NM_001254758.1:c.772-1519T>C	NP_001241687.1:n.772-1519T>C
NM_001254759.1:c.769-1519T>C	NP_001241688.1:n.769-1519T>C
NM_006278.2:c.760-1519T>C	NP_006269.1:n.760-1519T>C
XM_011542959.1:c.771+2575T>C	XP_011541261.1:n.771+2575T>C
XM_011542960.1:c.771+2575T>C	XP_011541262.1:n.771+2575T>C
XM_011542961.1:c.771+2575T>C	XP_011541263.1:n.771+2575T>C
XM_011542962.1:c.771+2575T>C	XP_011541264.1:n.771+2575T>C
NM_001348396.1:c.835-1519T>C	NP_001335325.1:n.835-1519T>C
NM_001348397.1:c.835-1519T>C	NP_001335326.1:n.835-1519T>C
NM_001348398.1:c.760-1601T>C	NP_001335327.1:n.760-1601T>C
NM_001348399.1:c.772-1519T>C	NP_001335328.1:n.772-1519T>C
NM_001348400.1:c.760-1519T>C	NP_001335329.1:n.760-1519T>C
NR_145671.1:n.1030-1344T>C
XM_024448658.1:c.772-1519T>C	XP_024304426.1:n.772-1519T>C
XM_024448659.1:c.772-1519T>C	XP_024304427.1:n.772-1519T>C
XM_024448660.1:c.772-1519T>C	XP_024304428.1:n.772-1519T>C
NM_001254757.2:c.772-1519T>C MANE Select	NP_001241686.1:n.772-1519T>C
NM_001254759.2:c.769-1519T>C	NP_001241688.1:n.769-1519T>C
NM_001348396.2:c.835-1519T>C	NP_001335325.1:n.835-1519T>C
NM_001348397.2:c.835-1519T>C	NP_001335326.1:n.835-1519T>C
NM_001348398.2:c.760-1601T>C	NP_001335327.1:n.760-1601T>C
NM_001348399.2:c.772-1519T>C	NP_001335328.1:n.772-1519T>C
NM_001348400.2:c.760-1519T>C	NP_001335329.1:n.760-1519T>C
NM_006278.3:c.760-1519T>C	NP_006269.1:n.760-1519T>C
NR_145671.2:n.989-1344T>C
NM_001254758.2:c.772-1519T>C	NP_001241687.1:n.772-1519T>C