Canonical Allele Identifier: CA383457813

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750630T>A (hg19) ; chr11:g.130880735T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880735T>A , CM000673.2:g.130880735T>A	GRCh38
NC_000011.9:g.130750630T>A , CM000673.1:g.130750630T>A	GRCh37
NC_000011.8:g.130255840T>A	NCBI36
NG_053190.1:g.40754A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2645A>T MANE Select	ENSP00000265909.4:p.Glu882Val
ENST00000265909.8:c.2645A>T	ENSP00000265909.4:p.Glu882Val
ENST00000426933.6:c.149A>T	ENSP00000413345.2:p.Glu50Val
ENST00000526579.5:n.178-1024A>T
ENST00000527116.5:n.407A>T
ENST00000528555.5:c.785A>T	ENSP00000435122.1:p.Glu262Val
ENST00000530330.1:n.381A>T
ENST00000530356.5:c.785A>T	ENSP00000432307.1:p.Glu262Val
ENST00000533318.5:n.1005A>T
ENST00000534726.5:c.365A>T	ENSP00000433699.1:p.Glu122Val
NM_001301089.1:c.785A>T	NP_001288018.1:p.Glu262Val
NM_014758.2:c.2645A>T	NP_055573.2:p.Glu882Val
XM_005271546.3:c.2574-1024A>T	XP_005271603.1:n.2574-1024A>T
XM_011542819.1:c.2891A>T	XP_011541121.1:p.Glu964Val
XM_011542820.1:c.2879A>T	XP_011541122.1:p.Glu960Val
XM_011542821.1:c.2771A>T	XP_011541123.1:p.Glu924Val
XM_011542824.1:c.2009A>T	XP_011541126.1:p.Glu670Val
XM_011542825.1:c.1166A>T	XP_011541127.1:p.Glu389Val
XM_011542826.1:c.1031A>T	XP_011541128.1:p.Glu344Val
XM_011542827.1:c.911A>T	XP_011541129.1:p.Glu304Val
NM_001347918.1:c.2525A>T	NP_001334847.1:p.Glu842Val
NM_001347919.1:c.2574-1024A>T	NP_001334848.1:n.2574-1024A>T
NM_001347922.1:c.974A>T	NP_001334851.1:p.Glu325Val
NM_001347923.1:c.920A>T	NP_001334852.1:p.Glu307Val
NM_001347924.1:c.665A>T	NP_001334853.1:p.Glu222Val
NM_001347925.1:c.611A>T	NP_001334854.1:p.Glu204Val
NM_001347926.1:c.714-1024A>T	NP_001334855.1:n.714-1024A>T
NM_001347927.1:c.365A>T	NP_001334856.1:p.Glu122Val
NR_144939.1:n.3278A>T
XM_011542820.2:c.2879A>T	XP_011541122.1:p.Glu960Val
XM_011542821.3:c.2771A>T	XP_011541123.1:p.Glu924Val
XM_011542824.2:c.2009A>T	XP_011541126.1:p.Glu670Val
XM_011542825.2:c.1166A>T	XP_011541127.1:p.Glu389Val
XM_011542826.2:c.1031A>T	XP_011541128.1:p.Glu344Val
XM_024448521.1:c.2891A>T	XP_024304289.1:p.Glu964Val
XR_001747870.1:n.3716A>T
XR_001747872.1:n.3062A>T
XR_001747873.1:n.3376A>T
NM_001301089.2:c.785A>T	NP_001288018.1:p.Glu262Val
NM_001347918.2:c.2525A>T	NP_001334847.2:p.Glu842Val
NM_001347919.2:c.2574-1024A>T	NP_001334848.2:n.2574-1024A>T
NM_001347920.2:c.*21041A>T	NP_001334849.2:n.*21041A>T
NM_001347922.2:c.974A>T	NP_001334851.2:p.Glu325Val
NM_001347923.2:c.920A>T	NP_001334852.2:p.Glu307Val
NM_001347924.2:c.665A>T	NP_001334853.1:p.Glu222Val
NM_001347925.2:c.611A>T	NP_001334854.1:p.Glu204Val
NM_001347926.2:c.714-1024A>T	NP_001334855.1:n.714-1024A>T
NM_001347927.2:c.365A>T	NP_001334856.1:p.Glu122Val
NM_014758.3:c.2645A>T MANE Select	NP_055573.3:p.Glu882Val
NR_144939.2:n.3270A>T