Canonical Allele Identifier: CA340862583

Gene: ST6GALNAC5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77044499A>G , CM000663.2:g.77044499A>G	GRCh38
NC_000001.10:g.77510184A>G , CM000663.1:g.77510184A>G	GRCh37
NC_000001.9:g.77282772A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477717.6:c.557A>G MANE Select	ENSP00000417583.1:p.Tyr186Cys
ENST00000318803.6:c.557A>G	ENSP00000436263.1:p.Tyr186Cys
ENST00000477717.5:c.557A>G	ENSP00000417583.1:p.Tyr186Cys
ENST00000488940.1:n.360A>G
NM_030965.1:c.557A>G	NP_112227.1:p.Tyr186Cys
XM_005271238.2:c.557A>G	XP_005271295.1:p.Tyr186Cys
XR_946772.1:n.792A>G
NM_001320273.1:c.262-5759A>G	NP_001307202.1:n.262-5759A>G
NM_001320274.1:c.262-18476A>G	NP_001307203.1:n.262-18476A>G
NM_030965.2:c.557A>G	NP_112227.1:p.Tyr186Cys
XR_001737460.2:n.784A>G
NM_030965.3:c.557A>G MANE Select	NP_112227.1:p.Tyr186Cys
NM_001320273.2:c.262-5759A>G	NP_001307202.1:n.262-5759A>G
NM_001320274.2:c.262-18476A>G	NP_001307203.1:n.262-18476A>G