Canonical Allele Identifier: CA2741220842

Gene: SNX19

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880716_130880718del , CM000673.2:g.130880716_130880718del	GRCh38
NC_000011.9:g.130750611_130750613del , CM000673.1:g.130750611_130750613del	GRCh37
NC_000011.8:g.130255821_130255823del	NCBI36
NG_053190.1:g.40772_40774del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2663_2665del MANE Select	ENSP00000265909.4:p.Gly888del
ENST00000265909.8:c.2663_2665del	ENSP00000265909.4:p.Gly888del
ENST00000426933.6:c.167_169del	ENSP00000413345.2:p.Gly56del
ENST00000526579.5:n.178-1006_178-1004del
ENST00000527116.5:n.425_427del
ENST00000528555.5:c.803_805del	ENSP00000435122.1:p.Gly268del
ENST00000530330.1:n.399_401del
ENST00000530356.5:c.803_805del	ENSP00000432307.1:p.Gly268del
ENST00000533318.5:n.1023_1025del
ENST00000534726.5:c.383_385del	ENSP00000433699.1:p.Gly128del
NM_001301089.1:c.803_805del	NP_001288018.1:p.Gly268del
NM_014758.2:c.2663_2665del	NP_055573.2:p.Gly888del
XM_005271546.3:c.2574-1006_2574-1004del	XP_005271603.1:n.2574-1006_2574-1004del
XM_011542819.1:c.2909_2911del	XP_011541121.1:p.Gly970del
XM_011542820.1:c.2897_2899del	XP_011541122.1:p.Gly966del
XM_011542821.1:c.2789_2791del	XP_011541123.1:p.Gly930del
XM_011542824.1:c.2027_2029del	XP_011541126.1:p.Gly676del
XM_011542825.1:c.1184_1186del	XP_011541127.1:p.Gly395del
XM_011542826.1:c.1049_1051del	XP_011541128.1:p.Gly350del
XM_011542827.1:c.929_931del	XP_011541129.1:p.Gly310del
NM_001347918.1:c.2543_2545del	NP_001334847.1:p.Gly848del
NM_001347919.1:c.2574-1006_2574-1004del	NP_001334848.1:n.2574-1006_2574-1004del
NM_001347922.1:c.992_994del	NP_001334851.1:p.Gly331del
NM_001347923.1:c.938_940del	NP_001334852.1:p.Gly313del
NM_001347924.1:c.683_685del	NP_001334853.1:p.Gly228del
NM_001347925.1:c.629_631del	NP_001334854.1:p.Gly210del
NM_001347926.1:c.714-1006_714-1004del	NP_001334855.1:n.714-1006_714-1004del
NM_001347927.1:c.383_385del	NP_001334856.1:p.Gly128del
NR_144939.1:n.3296_3298del
XM_011542820.2:c.2897_2899del	XP_011541122.1:p.Gly966del
XM_011542821.3:c.2789_2791del	XP_011541123.1:p.Gly930del
XM_011542824.2:c.2027_2029del	XP_011541126.1:p.Gly676del
XM_011542825.2:c.1184_1186del	XP_011541127.1:p.Gly395del
XM_011542826.2:c.1049_1051del	XP_011541128.1:p.Gly350del
XM_024448521.1:c.2909_2911del	XP_024304289.1:p.Gly970del
XR_001747870.1:n.3734_3736del
XR_001747872.1:n.3080_3082del
XR_001747873.1:n.3394_3396del
NM_001301089.2:c.803_805del	NP_001288018.1:p.Gly268del
NM_001347918.2:c.2543_2545del	NP_001334847.2:p.Gly848del
NM_001347919.2:c.2574-1006_2574-1004del	NP_001334848.2:n.2574-1006_2574-1004del
NM_001347920.2:c.*21059_*21061del	NP_001334849.2:n.*21059_*21061del
NM_001347922.2:c.992_994del	NP_001334851.2:p.Gly331del
NM_001347923.2:c.938_940del	NP_001334852.2:p.Gly313del
NM_001347924.2:c.683_685del	NP_001334853.1:p.Gly228del
NM_001347925.2:c.629_631del	NP_001334854.1:p.Gly210del
NM_001347926.2:c.714-1006_714-1004del	NP_001334855.1:n.714-1006_714-1004del
NM_001347927.2:c.383_385del	NP_001334856.1:p.Gly128del
NM_014758.3:c.2663_2665del MANE Select	NP_055573.3:p.Gly888del
NR_144939.2:n.3288_3290del