Canonical Allele Identifier: CA2009229771

Gene: SNX19

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880710_130880711delinsCA , CM000673.2:g.130880710_130880711delinsCA	GRCh38
NC_000011.9:g.130750605_130750606delinsCA , CM000673.1:g.130750605_130750606delinsCA	GRCh37
NC_000011.8:g.130255815_130255816delinsCA	NCBI36
NG_053190.1:g.40778_40779delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2669_2670delinsTG MANE Select	ENSP00000265909.4:p.Leu890=
ENST00000265909.8:c.2669_2670delinsTG	ENSP00000265909.4:p.Leu890=
ENST00000426933.6:c.173_174delinsTG	ENSP00000413345.2:p.Leu58=
ENST00000526579.5:n.178-1000_178-999delinsTG
ENST00000527116.5:n.431_432delinsTG
ENST00000528555.5:c.809_810delinsTG	ENSP00000435122.1:p.Leu270=
ENST00000530330.1:n.405_406delinsTG
ENST00000530356.5:c.809_810delinsTG	ENSP00000432307.1:p.Leu270=
ENST00000533318.5:n.1029_1030delinsTG
ENST00000534726.5:c.389_390delinsTG	ENSP00000433699.1:p.Leu130=
NM_001301089.1:c.809_810delinsTG	NP_001288018.1:p.Leu270=
NM_014758.2:c.2669_2670delinsTG	NP_055573.2:p.Leu890=
XM_005271546.3:c.2574-1000_2574-999delinsTG	XP_005271603.1:n.2574-1000_2574-999delinsTG
XM_011542819.1:c.2915_2916delinsTG	XP_011541121.1:p.Leu972=
XM_011542820.1:c.2903_2904delinsTG	XP_011541122.1:p.Leu968=
XM_011542821.1:c.2795_2796delinsTG	XP_011541123.1:p.Leu932=
XM_011542824.1:c.2033_2034delinsTG	XP_011541126.1:p.Leu678=
XM_011542825.1:c.1190_1191delinsTG	XP_011541127.1:p.Leu397=
XM_011542826.1:c.1055_1056delinsTG	XP_011541128.1:p.Leu352=
XM_011542827.1:c.935_936delinsTG	XP_011541129.1:p.Leu312=
NM_001347918.1:c.2549_2550delinsTG	NP_001334847.1:p.Leu850=
NM_001347919.1:c.2574-1000_2574-999delinsTG	NP_001334848.1:n.2574-1000_2574-999delinsTG
NM_001347922.1:c.998_999delinsTG	NP_001334851.1:p.Leu333=
NM_001347923.1:c.944_945delinsTG	NP_001334852.1:p.Leu315=
NM_001347924.1:c.689_690delinsTG	NP_001334853.1:p.Leu230=
NM_001347925.1:c.635_636delinsTG	NP_001334854.1:p.Leu212=
NM_001347926.1:c.714-1000_714-999delinsTG	NP_001334855.1:n.714-1000_714-999delinsTG
NM_001347927.1:c.389_390delinsTG	NP_001334856.1:p.Leu130=
NR_144939.1:n.3302_3303delinsTG
XM_011542820.2:c.2903_2904delinsTG	XP_011541122.1:p.Leu968=
XM_011542821.3:c.2795_2796delinsTG	XP_011541123.1:p.Leu932=
XM_011542824.2:c.2033_2034delinsTG	XP_011541126.1:p.Leu678=
XM_011542825.2:c.1190_1191delinsTG	XP_011541127.1:p.Leu397=
XM_011542826.2:c.1055_1056delinsTG	XP_011541128.1:p.Leu352=
XM_024448521.1:c.2915_2916delinsTG	XP_024304289.1:p.Leu972=
XR_001747870.1:n.3740_3741delinsTG
XR_001747872.1:n.3086_3087delinsTG
XR_001747873.1:n.3400_3401delinsTG
NM_001301089.2:c.809_810delinsTG	NP_001288018.1:p.Leu270=
NM_001347918.2:c.2549_2550delinsTG	NP_001334847.2:p.Leu850=
NM_001347919.2:c.2574-1000_2574-999delinsTG	NP_001334848.2:n.2574-1000_2574-999delinsTG
NM_001347920.2:c.*21065_*21066delinsTG	NP_001334849.2:n.*21065_*21066delinsTG
NM_001347922.2:c.998_999delinsTG	NP_001334851.2:p.Leu333=
NM_001347923.2:c.944_945delinsTG	NP_001334852.2:p.Leu315=
NM_001347924.2:c.689_690delinsTG	NP_001334853.1:p.Leu230=
NM_001347925.2:c.635_636delinsTG	NP_001334854.1:p.Leu212=
NM_001347926.2:c.714-1000_714-999delinsTG	NP_001334855.1:n.714-1000_714-999delinsTG
NM_001347927.2:c.389_390delinsTG	NP_001334856.1:p.Leu130=
NM_014758.3:c.2669_2670delinsTG MANE Select	NP_055573.3:p.Leu890=
NR_144939.2:n.3294_3295delinsTG