Canonical Allele Identifier: CA15514151

Gene: SNX13

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17879635G>T , CM000669.2:g.17879635G>T	GRCh38
NC_000007.13:g.17919258G>T , CM000669.1:g.17919258G>T	GRCh37
NC_000007.12:g.17885783G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409076.6:c.*139-3845C>A	ENSP00000387053.2:n.*139-3845C>A
ENST00000409604.1:c.*3179C>A	ENSP00000386639.1:n.*3179C>A
ENST00000428135.7:c.441-3845C>A MANE Select	ENSP00000398789.2:n.441-3845C>A
ENST00000444712.5:c.*206-3845C>A	ENSP00000397768.1:n.*206-3845C>A
ENST00000482558.5:n.618-3845C>A
ENST00000611725.4:c.441-3845C>A	ENSP00000479044.1:n.441-3845C>A
NM_015132.4:c.441-3845C>A	NP_055947.1:n.441-3845C>A
XM_005249672.1:c.441-3845C>A	XP_005249729.1:n.441-3845C>A
XM_005249673.3:c.441-3845C>A	XP_005249730.1:n.441-3845C>A
XM_005249674.3:c.441-3845C>A	XP_005249731.1:n.441-3845C>A
XM_011515229.1:c.441-3845C>A	XP_011513531.1:n.441-3845C>A
XM_011515230.1:c.201-3845C>A	XP_011513532.1:n.201-3845C>A
XM_011515231.1:c.201-3845C>A	XP_011513533.1:n.201-3845C>A
XM_011515232.1:c.201-3845C>A	XP_011513534.1:n.201-3845C>A
XM_011515233.1:c.134+1332C>A	XP_011513535.1:n.134+1332C>A
NM_001350862.1:c.441-3845C>A	NP_001337791.1:n.441-3845C>A
NM_001350863.1:c.201-3845C>A	NP_001337792.1:n.201-3845C>A
NM_001350864.1:c.134+1332C>A	NP_001337793.1:n.134+1332C>A
NM_001350866.1:c.-169-3845C>A	NP_001337795.1:n.-169-3845C>A
NM_001350867.1:c.-169-3845C>A	NP_001337796.1:n.-169-3845C>A
NM_001350868.1:c.441-3845C>A	NP_001337797.1:n.441-3845C>A
NM_001350870.1:c.*3179C>A	NP_001337799.1:n.*3179C>A
NR_146932.1:n.654-3845C>A
NR_146933.1:n.654-3845C>A
XM_005249673.5:c.441-3845C>A	XP_005249730.1:n.441-3845C>A
XM_011515229.2:c.441-3845C>A	XP_011513531.1:n.441-3845C>A
XM_011515230.2:c.201-3845C>A	XP_011513532.1:n.201-3845C>A
XM_011515231.2:c.201-3845C>A	XP_011513533.1:n.201-3845C>A
XM_011515233.3:c.134+1332C>A	XP_011513535.1:n.134+1332C>A
XM_017011893.2:c.441-3845C>A	XP_016867382.1:n.441-3845C>A
XM_017011894.2:c.201-3845C>A	XP_016867383.1:n.201-3845C>A
XM_017011896.2:c.53+1332C>A	XP_016867385.1:n.53+1332C>A
XM_024446696.1:c.53+1332C>A	XP_024302464.1:n.53+1332C>A
NM_015132.5:c.441-3845C>A MANE Select	NP_055947.1:n.441-3845C>A
NM_001350862.2:c.441-3845C>A	NP_001337791.1:n.441-3845C>A
NM_001350863.2:c.201-3845C>A	NP_001337792.1:n.201-3845C>A
NM_001350864.2:c.134+1332C>A	NP_001337793.1:n.134+1332C>A
NM_001350866.2:c.-169-3845C>A	NP_001337795.1:n.-169-3845C>A
NM_001350867.2:c.-169-3845C>A	NP_001337796.1:n.-169-3845C>A
NM_001350870.2:c.*3179C>A	NP_001337799.1:n.*3179C>A
NR_146932.2:n.640-3845C>A
NR_146933.2:n.640-3845C>A
NM_001350868.2:c.441-3845C>A	NP_001337797.1:n.441-3845C>A