Canonical Allele Identifier: CA383457744

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750597A>T (hg19) ; chr11:g.130880702A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880702A>T , CM000673.2:g.130880702A>T	GRCh38
NC_000011.9:g.130750597A>T , CM000673.1:g.130750597A>T	GRCh37
NC_000011.8:g.130255807A>T	NCBI36
NG_053190.1:g.40787T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2678T>A MANE Select	ENSP00000265909.4:p.Phe893Tyr
ENST00000265909.8:c.2678T>A	ENSP00000265909.4:p.Phe893Tyr
ENST00000426933.6:c.182T>A	ENSP00000413345.2:p.Phe61Tyr
ENST00000526579.5:n.178-991T>A
ENST00000527116.5:n.440T>A
ENST00000528555.5:c.818T>A	ENSP00000435122.1:p.Phe273Tyr
ENST00000530330.1:n.414T>A
ENST00000530356.5:c.818T>A	ENSP00000432307.1:p.Phe273Tyr
ENST00000533318.5:n.1038T>A
ENST00000534726.5:c.398T>A	ENSP00000433699.1:p.Phe133Tyr
NM_001301089.1:c.818T>A	NP_001288018.1:p.Phe273Tyr
NM_014758.2:c.2678T>A	NP_055573.2:p.Phe893Tyr
XM_005271546.3:c.2574-991T>A	XP_005271603.1:n.2574-991T>A
XM_011542819.1:c.2924T>A	XP_011541121.1:p.Phe975Tyr
XM_011542820.1:c.2912T>A	XP_011541122.1:p.Phe971Tyr
XM_011542821.1:c.2804T>A	XP_011541123.1:p.Phe935Tyr
XM_011542824.1:c.2042T>A	XP_011541126.1:p.Phe681Tyr
XM_011542825.1:c.1199T>A	XP_011541127.1:p.Phe400Tyr
XM_011542826.1:c.1064T>A	XP_011541128.1:p.Phe355Tyr
XM_011542827.1:c.944T>A	XP_011541129.1:p.Phe315Tyr
NM_001347918.1:c.2558T>A	NP_001334847.1:p.Phe853Tyr
NM_001347919.1:c.2574-991T>A	NP_001334848.1:n.2574-991T>A
NM_001347922.1:c.1007T>A	NP_001334851.1:p.Phe336Tyr
NM_001347923.1:c.953T>A	NP_001334852.1:p.Phe318Tyr
NM_001347924.1:c.698T>A	NP_001334853.1:p.Phe233Tyr
NM_001347925.1:c.644T>A	NP_001334854.1:p.Phe215Tyr
NM_001347926.1:c.714-991T>A	NP_001334855.1:n.714-991T>A
NM_001347927.1:c.398T>A	NP_001334856.1:p.Phe133Tyr
NR_144939.1:n.3311T>A
XM_011542820.2:c.2912T>A	XP_011541122.1:p.Phe971Tyr
XM_011542821.3:c.2804T>A	XP_011541123.1:p.Phe935Tyr
XM_011542824.2:c.2042T>A	XP_011541126.1:p.Phe681Tyr
XM_011542825.2:c.1199T>A	XP_011541127.1:p.Phe400Tyr
XM_011542826.2:c.1064T>A	XP_011541128.1:p.Phe355Tyr
XM_024448521.1:c.2924T>A	XP_024304289.1:p.Phe975Tyr
XR_001747870.1:n.3749T>A
XR_001747872.1:n.3095T>A
XR_001747873.1:n.3409T>A
NM_001301089.2:c.818T>A	NP_001288018.1:p.Phe273Tyr
NM_001347918.2:c.2558T>A	NP_001334847.2:p.Phe853Tyr
NM_001347919.2:c.2574-991T>A	NP_001334848.2:n.2574-991T>A
NM_001347920.2:c.*21074T>A	NP_001334849.2:n.*21074T>A
NM_001347922.2:c.1007T>A	NP_001334851.2:p.Phe336Tyr
NM_001347923.2:c.953T>A	NP_001334852.2:p.Phe318Tyr
NM_001347924.2:c.698T>A	NP_001334853.1:p.Phe233Tyr
NM_001347925.2:c.644T>A	NP_001334854.1:p.Phe215Tyr
NM_001347926.2:c.714-991T>A	NP_001334855.1:n.714-991T>A
NM_001347927.2:c.398T>A	NP_001334856.1:p.Phe133Tyr
NM_014758.3:c.2678T>A MANE Select	NP_055573.3:p.Phe893Tyr
NR_144939.2:n.3303T>A