Canonical Allele Identifier: CA6355236

Gene: ST3GAL4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126406065T>C , CM000673.2:g.126406065T>C	GRCh38
NC_000011.9:g.126275960T>C , CM000673.1:g.126275960T>C	GRCh37
NC_000011.8:g.125781170T>C	NCBI36
NG_053025.1:g.55421T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356132.9:c.4-31T>C	ENSP00000348451.5:n.4-31T>C
ENST00000444328.7:c.-60-31T>C MANE Select	ENSP00000394354.2:n.-60-31T>C
ENST00000676545.1:c.-60-31T>C	ENSP00000503901.1:n.-60-31T>C
ENST00000676867.1:c.-60-31T>C	ENSP00000503991.1:n.-60-31T>C
ENST00000677503.1:c.-60-31T>C	ENSP00000504548.1:n.-60-31T>C
ENST00000677721.1:c.-60-31T>C	ENSP00000502908.1:n.-60-31T>C
ENST00000678865.1:c.-60-31T>C	ENSP00000504245.1:n.-60-31T>C
ENST00000227495.10:c.-60-31T>C	ENSP00000227495.6:n.-60-31T>C
ENST00000356132.8:c.-60-31T>C	ENSP00000348451.4:n.-60-31T>C
ENST00000392669.6:c.-60-31T>C	ENSP00000376437.2:n.-60-31T>C
ENST00000444328.6:c.-60-31T>C	ENSP00000394354.2:n.-60-31T>C
ENST00000526311.5:c.-60-31T>C	ENSP00000432647.1:n.-60-31T>C
ENST00000526727.5:c.-91T>C	ENSP00000436047.1:n.-91T>C
ENST00000526756.5:n.114-31T>C
ENST00000528605.5:n.106-31T>C
ENST00000528858.5:c.-60-31T>C	ENSP00000432424.1:n.-60-31T>C
ENST00000530591.5:c.-60-31T>C	ENSP00000433989.1:n.-60-31T>C
ENST00000531217.5:c.-60-31T>C	ENSP00000432929.1:n.-60-31T>C
ENST00000534083.5:c.-60-31T>C	ENSP00000433318.1:n.-60-31T>C
ENST00000534452.5:c.-60-31T>C	ENSP00000434756.1:n.-60-31T>C
ENST00000534733.6:c.88-31T>C	ENSP00000433495.2:n.88-31T>C
NM_001254757.1:c.-60-31T>C	NP_001241686.1:n.-60-31T>C
NM_001254758.1:c.-60-31T>C	NP_001241687.1:n.-60-31T>C
NM_006278.2:c.-60-31T>C	NP_006269.1:n.-60-31T>C
NM_001348396.1:c.4-31T>C	NP_001335325.1:n.4-31T>C
NM_001348397.1:c.4-31T>C	NP_001335326.1:n.4-31T>C
NM_001348398.1:c.-60-31T>C	NP_001335327.1:n.-60-31T>C
NM_001348399.1:c.-60-31T>C	NP_001335328.1:n.-60-31T>C
NM_001348400.1:c.-60-31T>C	NP_001335329.1:n.-60-31T>C
NR_145671.1:n.199-31T>C
XM_024448658.1:c.-60-31T>C	XP_024304426.1:n.-60-31T>C
XM_024448659.1:c.-60-31T>C	XP_024304427.1:n.-60-31T>C
XM_024448660.1:c.-60-31T>C	XP_024304428.1:n.-60-31T>C
NM_001254757.2:c.-60-31T>C MANE Select	NP_001241686.1:n.-60-31T>C
NM_001348396.2:c.4-31T>C	NP_001335325.1:n.4-31T>C
NM_001348397.2:c.4-31T>C	NP_001335326.1:n.4-31T>C
NM_001348398.2:c.-60-31T>C	NP_001335327.1:n.-60-31T>C
NM_001348399.2:c.-60-31T>C	NP_001335328.1:n.-60-31T>C
NM_001348400.2:c.-60-31T>C	NP_001335329.1:n.-60-31T>C
NM_006278.3:c.-60-31T>C	NP_006269.1:n.-60-31T>C
NR_145671.2:n.158-31T>C
NM_001254758.2:c.-60-31T>C	NP_001241687.1:n.-60-31T>C