Canonical Allele Identifier: CA1299365741

Gene: GALNT13

Linked Data

• dbSNP Id: rs1042328770

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.153969905C>T , CM000664.2:g.153969905C>T	GRCh38
NC_000002.11:g.154826418C>T , CM000664.1:g.154826418C>T	GRCh37
NC_000002.10:g.154534664C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000392825.8:c.142+25266C>T MANE Select	ENSP00000376570.3:n.142+25266C>T
ENST00000392825.7:c.142+25266C>T	ENSP00000376570.3:n.142+25266C>T
ENST00000409237.5:c.142+25266C>T	ENSP00000387239.1:n.142+25266C>T
NM_001301627.1:c.142+25266C>T	NP_001288556.1:n.142+25266C>T
NM_052917.3:c.142+25266C>T	NP_443149.2:n.142+25266C>T
XM_011510537.1:c.142+25266C>T	XP_011508839.1:n.142+25266C>T
XM_011510537.3:c.142+25266C>T	XP_011508839.1:n.142+25266C>T
XM_017003258.1:c.142+25266C>T	XP_016858747.1:n.142+25266C>T
XM_017003259.1:c.142+25266C>T	XP_016858748.1:n.142+25266C>T
XM_017003260.2:c.142+25266C>T	XP_016858749.1:n.142+25266C>T
XM_017003261.1:c.142+25266C>T	XP_016858750.1:n.142+25266C>T
XM_024452643.1:c.-537+25266C>T	XP_024308411.1:n.-537+25266C>T
XR_001738598.2:n.700+25266C>T
XR_001738599.2:n.700+25266C>T
NM_052917.4:c.142+25266C>T MANE Select	NP_443149.2:n.142+25266C>T
NM_001301627.2:c.142+25266C>T	NP_001288556.1:n.142+25266C>T
NM_001376392.1:c.142+25266C>T	NP_001363321.1:n.142+25266C>T
NM_001376394.1:c.142+25266C>T	NP_001363323.1:n.142+25266C>T
NM_001376398.1:c.142+25266C>T	NP_001363327.1:n.142+25266C>T
NM_001376400.1:c.142+25266C>T	NP_001363329.1:n.142+25266C>T
NM_001376401.1:c.142+25266C>T	NP_001363330.1:n.142+25266C>T
NM_001376402.1:c.142+25266C>T	NP_001363331.1:n.142+25266C>T
NM_001376403.1:c.142+25266C>T	NP_001363332.1:n.142+25266C>T
NM_001376404.1:c.142+25266C>T	NP_001363333.1:n.142+25266C>T
NM_001376405.1:c.142+25266C>T	NP_001363334.1:n.142+25266C>T