Canonical Allele Identifier: CA2276065331

Gene: ST6GALNAC2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76578744C= , CM000679.2:g.76578744C=	GRCh38
NC_000017.10:g.74574826C= , CM000679.1:g.74574826C=	GRCh37
NC_000017.9:g.72086421C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006456.3:c.186+12G= MANE Select	NP_006447.2:n.186+12G=
ENST00000225276.10:c.186+12G= MANE Select	ENSP00000225276.4:n.186+12G=
NM_006456.2:c.186+12G=	NP_006447.2:n.186+12G=
ENST00000225276.9:c.186+12G=	ENSP00000225276.4:n.186+12G=
ENST00000585736.1:c.*43+12G=	ENSP00000466513.1:n.*43+12G=
ENST00000586520.5:n.235+12G=
ENST00000588005.5:n.149+12G=
ENST00000588120.5:c.126-4205G=	ENSP00000465778.1:n.126-4205G=
ENST00000592508.1:n.228+12G=
XM_005256954.3:c.186+12G=	XP_005257011.1:n.186+12G=
XM_005256954.4:c.186+12G=	XP_005257011.1:n.186+12G=
XM_011524200.1:c.186+12G=	XP_011522502.1:n.186+12G=
XR_001752403.2:n.506+12G=
XR_001752404.2:n.506+12G=
XR_001752405.2:n.506+12G=
XR_001752406.2:n.444+12G=
XR_001752407.2:n.444+12G=
XR_934349.1:n.444+12G=
XR_934349.2:n.506+12G=
XR_934350.1:n.444+12G=
XR_934351.1:n.444+12G=