Canonical Allele Identifier: CA2009229566

Gene: SNX19

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880603A= , CM000673.2:g.130880603A=	GRCh38
NC_000011.9:g.130750498A= , CM000673.1:g.130750498A=	GRCh37
NC_000011.8:g.130255708A=	NCBI36
NG_053190.1:g.40886T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2758+19T= MANE Select	ENSP00000265909.4:n.2758+19T=
ENST00000265909.8:c.2758+19T=	ENSP00000265909.4:n.2758+19T=
ENST00000426933.6:c.262+19T=	ENSP00000413345.2:n.262+19T=
ENST00000526579.5:n.178-892T=
ENST00000527116.5:n.520+19T=
ENST00000528555.5:c.898+19T=	ENSP00000435122.1:n.898+19T=
ENST00000530330.1:n.494+19T=
ENST00000530356.5:c.898+19T=	ENSP00000432307.1:n.898+19T=
ENST00000533318.5:n.1118+19T=
ENST00000534726.5:c.478+19T=	ENSP00000433699.1:n.478+19T=
NM_001301089.1:c.898+19T=	NP_001288018.1:n.898+19T=
NM_014758.2:c.2758+19T=	NP_055573.2:n.2758+19T=
XM_005271546.3:c.2574-892T=	XP_005271603.1:n.2574-892T=
XM_011542819.1:c.3004+19T=	XP_011541121.1:n.3004+19T=
XM_011542820.1:c.2992+19T=	XP_011541122.1:n.2992+19T=
XM_011542821.1:c.2884+19T=	XP_011541123.1:n.2884+19T=
XM_011542824.1:c.2122+19T=	XP_011541126.1:n.2122+19T=
XM_011542825.1:c.1279+19T=	XP_011541127.1:n.1279+19T=
XM_011542826.1:c.1144+19T=	XP_011541128.1:n.1144+19T=
XM_011542827.1:c.1024+19T=	XP_011541129.1:n.1024+19T=
NM_001347918.1:c.2638+19T=	NP_001334847.1:n.2638+19T=
NM_001347919.1:c.2574-892T=	NP_001334848.1:n.2574-892T=
NM_001347922.1:c.1087+19T=	NP_001334851.1:n.1087+19T=
NM_001347923.1:c.1033+19T=	NP_001334852.1:n.1033+19T=
NM_001347924.1:c.778+19T=	NP_001334853.1:n.778+19T=
NM_001347925.1:c.724+19T=	NP_001334854.1:n.724+19T=
NM_001347926.1:c.714-892T=	NP_001334855.1:n.714-892T=
NM_001347927.1:c.478+19T=	NP_001334856.1:n.478+19T=
NR_144939.1:n.3391+19T=
XM_011542820.2:c.2992+19T=	XP_011541122.1:n.2992+19T=
XM_011542821.3:c.2884+19T=	XP_011541123.1:n.2884+19T=
XM_011542824.2:c.2122+19T=	XP_011541126.1:n.2122+19T=
XM_011542825.2:c.1279+19T=	XP_011541127.1:n.1279+19T=
XM_011542826.2:c.1144+19T=	XP_011541128.1:n.1144+19T=
XM_024448521.1:c.3004+19T=	XP_024304289.1:n.3004+19T=
XR_001747870.1:n.3829+19T=
XR_001747872.1:n.3175+19T=
XR_001747873.1:n.3489+19T=
NM_001301089.2:c.898+19T=	NP_001288018.1:n.898+19T=
NM_001347918.2:c.2638+19T=	NP_001334847.2:n.2638+19T=
NM_001347919.2:c.2574-892T=	NP_001334848.2:n.2574-892T=
NM_001347920.2:c.*21173T=	NP_001334849.2:n.*21173T=
NM_001347922.2:c.1087+19T=	NP_001334851.2:n.1087+19T=
NM_001347923.2:c.1033+19T=	NP_001334852.2:n.1033+19T=
NM_001347924.2:c.778+19T=	NP_001334853.1:n.778+19T=
NM_001347925.2:c.724+19T=	NP_001334854.1:n.724+19T=
NM_001347926.2:c.714-892T=	NP_001334855.1:n.714-892T=
NM_001347927.2:c.478+19T=	NP_001334856.1:n.478+19T=
NM_014758.3:c.2758+19T= MANE Select	NP_055573.3:n.2758+19T=
NR_144939.2:n.3383+19T=