Canonical Allele Identifier: CA2009229800

Gene: SNX19

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880731G= , CM000673.2:g.130880731G=	GRCh38
NC_000011.9:g.130750626G= , CM000673.1:g.130750626G=	GRCh37
NC_000011.8:g.130255836G=	NCBI36
NG_053190.1:g.40758C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2649C= MANE Select	ENSP00000265909.4:p.Ser883=
ENST00000265909.8:c.2649C=	ENSP00000265909.4:p.Ser883=
ENST00000426933.6:c.153C=	ENSP00000413345.2:p.Ser51=
ENST00000526579.5:n.178-1020C=
ENST00000527116.5:n.411C=
ENST00000528555.5:c.789C=	ENSP00000435122.1:p.Ser263=
ENST00000530330.1:n.385C=
ENST00000530356.5:c.789C=	ENSP00000432307.1:p.Ser263=
ENST00000533318.5:n.1009C=
ENST00000534726.5:c.369C=	ENSP00000433699.1:p.Ser123=
NM_001301089.1:c.789C=	NP_001288018.1:p.Ser263=
NM_014758.2:c.2649C=	NP_055573.2:p.Ser883=
XM_005271546.3:c.2574-1020C=	XP_005271603.1:n.2574-1020C=
XM_011542819.1:c.2895C=	XP_011541121.1:p.Ser965=
XM_011542820.1:c.2883C=	XP_011541122.1:p.Ser961=
XM_011542821.1:c.2775C=	XP_011541123.1:p.Ser925=
XM_011542824.1:c.2013C=	XP_011541126.1:p.Ser671=
XM_011542825.1:c.1170C=	XP_011541127.1:p.Ser390=
XM_011542826.1:c.1035C=	XP_011541128.1:p.Ser345=
XM_011542827.1:c.915C=	XP_011541129.1:p.Ser305=
NM_001347918.1:c.2529C=	NP_001334847.1:p.Ser843=
NM_001347919.1:c.2574-1020C=	NP_001334848.1:n.2574-1020C=
NM_001347922.1:c.978C=	NP_001334851.1:p.Ser326=
NM_001347923.1:c.924C=	NP_001334852.1:p.Ser308=
NM_001347924.1:c.669C=	NP_001334853.1:p.Ser223=
NM_001347925.1:c.615C=	NP_001334854.1:p.Ser205=
NM_001347926.1:c.714-1020C=	NP_001334855.1:n.714-1020C=
NM_001347927.1:c.369C=	NP_001334856.1:p.Ser123=
NR_144939.1:n.3282C=
XM_011542820.2:c.2883C=	XP_011541122.1:p.Ser961=
XM_011542821.3:c.2775C=	XP_011541123.1:p.Ser925=
XM_011542824.2:c.2013C=	XP_011541126.1:p.Ser671=
XM_011542825.2:c.1170C=	XP_011541127.1:p.Ser390=
XM_011542826.2:c.1035C=	XP_011541128.1:p.Ser345=
XM_024448521.1:c.2895C=	XP_024304289.1:p.Ser965=
XR_001747870.1:n.3720C=
XR_001747872.1:n.3066C=
XR_001747873.1:n.3380C=
NM_001301089.2:c.789C=	NP_001288018.1:p.Ser263=
NM_001347918.2:c.2529C=	NP_001334847.2:p.Ser843=
NM_001347919.2:c.2574-1020C=	NP_001334848.2:n.2574-1020C=
NM_001347920.2:c.*21045C=	NP_001334849.2:n.*21045C=
NM_001347922.2:c.978C=	NP_001334851.2:p.Ser326=
NM_001347923.2:c.924C=	NP_001334852.2:p.Ser308=
NM_001347924.2:c.669C=	NP_001334853.1:p.Ser223=
NM_001347925.2:c.615C=	NP_001334854.1:p.Ser205=
NM_001347926.2:c.714-1020C=	NP_001334855.1:n.714-1020C=
NM_001347927.2:c.369C=	NP_001334856.1:p.Ser123=
NM_014758.3:c.2649C= MANE Select	NP_055573.3:p.Ser883=
NR_144939.2:n.3274C=