Canonical Allele Identifier: CA383457770

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750609A>T (hg19) ; chr11:g.130880714A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880714A>T , CM000673.2:g.130880714A>T	GRCh38
NC_000011.9:g.130750609A>T , CM000673.1:g.130750609A>T	GRCh37
NC_000011.8:g.130255819A>T	NCBI36
NG_053190.1:g.40775T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2666T>A MANE Select	ENSP00000265909.4:p.Val889Asp
ENST00000265909.8:c.2666T>A	ENSP00000265909.4:p.Val889Asp
ENST00000426933.6:c.170T>A	ENSP00000413345.2:p.Val57Asp
ENST00000526579.5:n.178-1003T>A
ENST00000527116.5:n.428T>A
ENST00000528555.5:c.806T>A	ENSP00000435122.1:p.Val269Asp
ENST00000530330.1:n.402T>A
ENST00000530356.5:c.806T>A	ENSP00000432307.1:p.Val269Asp
ENST00000533318.5:n.1026T>A
ENST00000534726.5:c.386T>A	ENSP00000433699.1:p.Val129Asp
NM_001301089.1:c.806T>A	NP_001288018.1:p.Val269Asp
NM_014758.2:c.2666T>A	NP_055573.2:p.Val889Asp
XM_005271546.3:c.2574-1003T>A	XP_005271603.1:n.2574-1003T>A
XM_011542819.1:c.2912T>A	XP_011541121.1:p.Val971Asp
XM_011542820.1:c.2900T>A	XP_011541122.1:p.Val967Asp
XM_011542821.1:c.2792T>A	XP_011541123.1:p.Val931Asp
XM_011542824.1:c.2030T>A	XP_011541126.1:p.Val677Asp
XM_011542825.1:c.1187T>A	XP_011541127.1:p.Val396Asp
XM_011542826.1:c.1052T>A	XP_011541128.1:p.Val351Asp
XM_011542827.1:c.932T>A	XP_011541129.1:p.Val311Asp
NM_001347918.1:c.2546T>A	NP_001334847.1:p.Val849Asp
NM_001347919.1:c.2574-1003T>A	NP_001334848.1:n.2574-1003T>A
NM_001347922.1:c.995T>A	NP_001334851.1:p.Val332Asp
NM_001347923.1:c.941T>A	NP_001334852.1:p.Val314Asp
NM_001347924.1:c.686T>A	NP_001334853.1:p.Val229Asp
NM_001347925.1:c.632T>A	NP_001334854.1:p.Val211Asp
NM_001347926.1:c.714-1003T>A	NP_001334855.1:n.714-1003T>A
NM_001347927.1:c.386T>A	NP_001334856.1:p.Val129Asp
NR_144939.1:n.3299T>A
XM_011542820.2:c.2900T>A	XP_011541122.1:p.Val967Asp
XM_011542821.3:c.2792T>A	XP_011541123.1:p.Val931Asp
XM_011542824.2:c.2030T>A	XP_011541126.1:p.Val677Asp
XM_011542825.2:c.1187T>A	XP_011541127.1:p.Val396Asp
XM_011542826.2:c.1052T>A	XP_011541128.1:p.Val351Asp
XM_024448521.1:c.2912T>A	XP_024304289.1:p.Val971Asp
XR_001747870.1:n.3737T>A
XR_001747872.1:n.3083T>A
XR_001747873.1:n.3397T>A
NM_001301089.2:c.806T>A	NP_001288018.1:p.Val269Asp
NM_001347918.2:c.2546T>A	NP_001334847.2:p.Val849Asp
NM_001347919.2:c.2574-1003T>A	NP_001334848.2:n.2574-1003T>A
NM_001347920.2:c.*21062T>A	NP_001334849.2:n.*21062T>A
NM_001347922.2:c.995T>A	NP_001334851.2:p.Val332Asp
NM_001347923.2:c.941T>A	NP_001334852.2:p.Val314Asp
NM_001347924.2:c.686T>A	NP_001334853.1:p.Val229Asp
NM_001347925.2:c.632T>A	NP_001334854.1:p.Val211Asp
NM_001347926.2:c.714-1003T>A	NP_001334855.1:n.714-1003T>A
NM_001347927.2:c.386T>A	NP_001334856.1:p.Val129Asp
NM_014758.3:c.2666T>A MANE Select	NP_055573.3:p.Val889Asp
NR_144939.2:n.3291T>A