Canonical Allele Identifier: CA1299558943

Gene: GALNT13

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.154377834A= , CM000664.2:g.154377834A=	GRCh38
NC_000002.11:g.155234346A= , CM000664.1:g.155234346A=	GRCh37
NC_000002.10:g.154942592A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000392825.8:c.1157-18157A= MANE Select	ENSP00000376570.3:n.1157-18157A=
ENST00000392825.7:c.1157-18157A=	ENSP00000376570.3:n.1157-18157A=
ENST00000409237.5:c.1157-18157A=	ENSP00000387239.1:n.1157-18157A=
ENST00000431076.5:c.1146-18157A=
ENST00000450838.5:c.12-18157A=
ENST00000487047.1:n.459-18157A=
NM_001301627.1:c.1157-18157A=	NP_001288556.1:n.1157-18157A=
NM_052917.3:c.1157-18157A=	NP_443149.2:n.1157-18157A=
XM_011510537.1:c.1157-18157A=	XP_011508839.1:n.1157-18157A=
XM_011510538.1:c.614-18157A=	XP_011508840.1:n.614-18157A=
XM_011510537.3:c.1157-18157A=	XP_011508839.1:n.1157-18157A=
XM_011510538.2:c.614-18157A=	XP_011508840.1:n.614-18157A=
XM_017003258.1:c.1157-18157A=	XP_016858747.1:n.1157-18157A=
XM_017003259.1:c.1157-18157A=	XP_016858748.1:n.1157-18157A=
XM_017003260.2:c.1157-18157A=	XP_016858749.1:n.1157-18157A=
XM_017003261.1:c.1157-18157A=	XP_016858750.1:n.1157-18157A=
XM_017003262.1:c.614-18157A=	XP_016858751.1:n.614-18157A=
XM_024452643.1:c.614-18157A=	XP_024308411.1:n.614-18157A=
XR_001738598.2:n.1597-18157A=
XR_001738599.2:n.1597-18157A=
NM_052917.4:c.1157-18157A= MANE Select	NP_443149.2:n.1157-18157A=
NM_001301627.2:c.1157-18157A=	NP_001288556.1:n.1157-18157A=
NM_001376392.1:c.1157-18157A=	NP_001363321.1:n.1157-18157A=
NM_001376394.1:c.1157-18157A=	NP_001363323.1:n.1157-18157A=
NM_001376398.1:c.1157-18157A=	NP_001363327.1:n.1157-18157A=
NM_001376400.1:c.1157-18157A=	NP_001363329.1:n.1157-18157A=
NM_001376401.1:c.1157-18157A=	NP_001363330.1:n.1157-18157A=
NM_001376402.1:c.1157-18157A=	NP_001363331.1:n.1157-18157A=
NM_001376403.1:c.1157-18157A=	NP_001363332.1:n.1157-18157A=
NM_001376404.1:c.1157-18157A=	NP_001363333.1:n.1157-18157A=
NM_001376405.1:c.1039-31150A=	NP_001363334.1:n.1039-31150A=