Canonical Allele Identifier: CA2616844395

Gene: SNX19

Linked Data

• gnomAD v4: 11-130880747-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880749del , CM000673.2:g.130880749del	GRCh38
NC_000011.9:g.130750644del , CM000673.1:g.130750644del	GRCh37
NC_000011.8:g.130255854del	NCBI36
NG_053190.1:g.40741del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2632del MANE Select	ENSP00000265909.4:p.Leu878CysfsTer20
ENST00000265909.8:c.2632del	ENSP00000265909.4:p.Leu878CysfsTer20
ENST00000426933.6:c.136del	ENSP00000413345.2:p.Leu46CysfsTer20
ENST00000526579.5:n.178-1037del
ENST00000527116.5:n.394del
ENST00000528555.5:c.772del	ENSP00000435122.1:p.Leu258CysfsTer20
ENST00000530330.1:n.368del
ENST00000530356.5:c.772del	ENSP00000432307.1:p.Leu258CysfsTer20
ENST00000533318.5:n.992del
ENST00000534726.5:c.352del	ENSP00000433699.1:p.Leu118CysfsTer20
NM_001301089.1:c.772del	NP_001288018.1:p.Leu258CysfsTer20
NM_014758.2:c.2632del	NP_055573.2:p.Leu878CysfsTer20
XM_005271546.3:c.2574-1037del	XP_005271603.1:n.2574-1037del
XM_011542819.1:c.2878del	XP_011541121.1:p.Leu960CysfsTer20
XM_011542820.1:c.2866del	XP_011541122.1:p.Leu956CysfsTer20
XM_011542821.1:c.2758del	XP_011541123.1:p.Leu920CysfsTer20
XM_011542824.1:c.1996del	XP_011541126.1:p.Leu666CysfsTer20
XM_011542825.1:c.1153del	XP_011541127.1:p.Leu385CysfsTer20
XM_011542826.1:c.1018del	XP_011541128.1:p.Leu340CysfsTer20
XM_011542827.1:c.898del	XP_011541129.1:p.Leu300CysfsTer20
NM_001347918.1:c.2512del	NP_001334847.1:p.Leu838CysfsTer20
NM_001347919.1:c.2574-1037del	NP_001334848.1:n.2574-1037del
NM_001347922.1:c.961del	NP_001334851.1:p.Leu321CysfsTer20
NM_001347923.1:c.907del	NP_001334852.1:p.Leu303CysfsTer20
NM_001347924.1:c.652del	NP_001334853.1:p.Leu218CysfsTer20
NM_001347925.1:c.598del	NP_001334854.1:p.Leu200CysfsTer20
NM_001347926.1:c.714-1037del	NP_001334855.1:n.714-1037del
NM_001347927.1:c.352del	NP_001334856.1:p.Leu118CysfsTer20
NR_144939.1:n.3265del
XM_011542820.2:c.2866del	XP_011541122.1:p.Leu956CysfsTer20
XM_011542821.3:c.2758del	XP_011541123.1:p.Leu920CysfsTer20
XM_011542824.2:c.1996del	XP_011541126.1:p.Leu666CysfsTer20
XM_011542825.2:c.1153del	XP_011541127.1:p.Leu385CysfsTer20
XM_011542826.2:c.1018del	XP_011541128.1:p.Leu340CysfsTer20
XM_024448521.1:c.2878del	XP_024304289.1:p.Leu960CysfsTer20
XR_001747870.1:n.3703del
XR_001747872.1:n.3049del
XR_001747873.1:n.3363del
NM_001301089.2:c.772del	NP_001288018.1:p.Leu258CysfsTer20
NM_001347918.2:c.2512del	NP_001334847.2:p.Leu838CysfsTer20
NM_001347919.2:c.2574-1037del	NP_001334848.2:n.2574-1037del
NM_001347920.2:c.*21028del	NP_001334849.2:n.*21028del
NM_001347922.2:c.961del	NP_001334851.2:p.Leu321CysfsTer20
NM_001347923.2:c.907del	NP_001334852.2:p.Leu303CysfsTer20
NM_001347924.2:c.652del	NP_001334853.1:p.Leu218CysfsTer20
NM_001347925.2:c.598del	NP_001334854.1:p.Leu200CysfsTer20
NM_001347926.2:c.714-1037del	NP_001334855.1:n.714-1037del
NM_001347927.2:c.352del	NP_001334856.1:p.Leu118CysfsTer20
NM_014758.3:c.2632del MANE Select	NP_055573.3:p.Leu878CysfsTer20
NR_144939.2:n.3257del