Canonical Allele Identifier: CA915300

Gene: ST6GALNAC5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.76868501A>G , CM000663.2:g.76868501A>G	GRCh38
NC_000001.10:g.77334186A>G , CM000663.1:g.77334186A>G	GRCh37
NC_000001.9:g.77106774A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477717.6:c.20A>G MANE Select	ENSP00000417583.1:p.His7Arg
ENST00000318803.6:c.20A>G	ENSP00000436263.1:p.His7Arg
ENST00000477717.5:c.20A>G	ENSP00000417583.1:p.His7Arg
ENST00000480428.1:n.216A>G
ENST00000496845.1:n.214A>G
NM_030965.1:c.20A>G	NP_112227.1:p.His7Arg
XM_005271238.2:c.20A>G	XP_005271295.1:p.His7Arg
XR_946772.1:n.255A>G
NM_001320273.1:c.20A>G	NP_001307202.1:p.His7Arg
NM_001320274.1:c.20A>G	NP_001307203.1:p.His7Arg
NM_030965.2:c.20A>G	NP_112227.1:p.His7Arg
XR_001737460.2:n.247A>G
NM_030965.3:c.20A>G MANE Select	NP_112227.1:p.His7Arg
NM_001320273.2:c.20A>G	NP_001307202.1:p.His7Arg
NM_001320274.2:c.20A>G	NP_001307203.1:p.His7Arg