Canonical Allele Identifier: CA477582336

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750659G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880764G>T , CM000673.2:g.130880764G>T	GRCh38
NC_000011.9:g.130750659G>T , CM000673.1:g.130750659G>T	GRCh37
NC_000011.8:g.130255869G>T	NCBI36
NG_053190.1:g.40725C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2616C>A MANE Select	ENSP00000265909.4:p.Arg872=
ENST00000265909.8:c.2616C>A	ENSP00000265909.4:p.Arg872=
ENST00000426933.6:c.120C>A	ENSP00000413345.2:p.Arg40=
ENST00000526579.5:n.178-1053C>A
ENST00000527116.5:n.378C>A
ENST00000528555.5:c.756C>A	ENSP00000435122.1:p.Arg252=
ENST00000530330.1:n.352C>A
ENST00000530356.5:c.756C>A	ENSP00000432307.1:p.Arg252=
ENST00000533318.5:n.976C>A
ENST00000534726.5:c.336C>A	ENSP00000433699.1:p.Arg112=
NM_001301089.1:c.756C>A	NP_001288018.1:p.Arg252=
NM_014758.2:c.2616C>A	NP_055573.2:p.Arg872=
XM_005271546.3:c.2574-1053C>A	XP_005271603.1:n.2574-1053C>A
XM_011542819.1:c.2862C>A	XP_011541121.1:p.Arg954=
XM_011542820.1:c.2850C>A	XP_011541122.1:p.Arg950=
XM_011542821.1:c.2742C>A	XP_011541123.1:p.Arg914=
XM_011542824.1:c.1980C>A	XP_011541126.1:p.Arg660=
XM_011542825.1:c.1137C>A	XP_011541127.1:p.Arg379=
XM_011542826.1:c.1002C>A	XP_011541128.1:p.Arg334=
XM_011542827.1:c.882C>A	XP_011541129.1:p.Arg294=
NM_001347918.1:c.2496C>A	NP_001334847.1:p.Arg832=
NM_001347919.1:c.2574-1053C>A	NP_001334848.1:n.2574-1053C>A
NM_001347922.1:c.945C>A	NP_001334851.1:p.Arg315=
NM_001347923.1:c.891C>A	NP_001334852.1:p.Arg297=
NM_001347924.1:c.636C>A	NP_001334853.1:p.Arg212=
NM_001347925.1:c.582C>A	NP_001334854.1:p.Arg194=
NM_001347926.1:c.714-1053C>A	NP_001334855.1:n.714-1053C>A
NM_001347927.1:c.336C>A	NP_001334856.1:p.Arg112=
NR_144939.1:n.3249C>A
XM_011542820.2:c.2850C>A	XP_011541122.1:p.Arg950=
XM_011542821.3:c.2742C>A	XP_011541123.1:p.Arg914=
XM_011542824.2:c.1980C>A	XP_011541126.1:p.Arg660=
XM_011542825.2:c.1137C>A	XP_011541127.1:p.Arg379=
XM_011542826.2:c.1002C>A	XP_011541128.1:p.Arg334=
XM_024448521.1:c.2862C>A	XP_024304289.1:p.Arg954=
XR_001747870.1:n.3687C>A
XR_001747872.1:n.3033C>A
XR_001747873.1:n.3347C>A
NM_001301089.2:c.756C>A	NP_001288018.1:p.Arg252=
NM_001347918.2:c.2496C>A	NP_001334847.2:p.Arg832=
NM_001347919.2:c.2574-1053C>A	NP_001334848.2:n.2574-1053C>A
NM_001347920.2:c.*21012C>A	NP_001334849.2:n.*21012C>A
NM_001347922.2:c.945C>A	NP_001334851.2:p.Arg315=
NM_001347923.2:c.891C>A	NP_001334852.2:p.Arg297=
NM_001347924.2:c.636C>A	NP_001334853.1:p.Arg212=
NM_001347925.2:c.582C>A	NP_001334854.1:p.Arg194=
NM_001347926.2:c.714-1053C>A	NP_001334855.1:n.714-1053C>A
NM_001347927.2:c.336C>A	NP_001334856.1:p.Arg112=
NM_014758.3:c.2616C>A MANE Select	NP_055573.3:p.Arg872=
NR_144939.2:n.3241C>A