Canonical Allele Identifier: CA383457767

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750607A>T (hg19) ; chr11:g.130880712A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880712A>T , CM000673.2:g.130880712A>T	GRCh38
NC_000011.9:g.130750607A>T , CM000673.1:g.130750607A>T	GRCh37
NC_000011.8:g.130255817A>T	NCBI36
NG_053190.1:g.40777T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2668T>A MANE Select	ENSP00000265909.4:p.Leu890Met
ENST00000265909.8:c.2668T>A	ENSP00000265909.4:p.Leu890Met
ENST00000426933.6:c.172T>A	ENSP00000413345.2:p.Leu58Met
ENST00000526579.5:n.178-1001T>A
ENST00000527116.5:n.430T>A
ENST00000528555.5:c.808T>A	ENSP00000435122.1:p.Leu270Met
ENST00000530330.1:n.404T>A
ENST00000530356.5:c.808T>A	ENSP00000432307.1:p.Leu270Met
ENST00000533318.5:n.1028T>A
ENST00000534726.5:c.388T>A	ENSP00000433699.1:p.Leu130Met
NM_001301089.1:c.808T>A	NP_001288018.1:p.Leu270Met
NM_014758.2:c.2668T>A	NP_055573.2:p.Leu890Met
XM_005271546.3:c.2574-1001T>A	XP_005271603.1:n.2574-1001T>A
XM_011542819.1:c.2914T>A	XP_011541121.1:p.Leu972Met
XM_011542820.1:c.2902T>A	XP_011541122.1:p.Leu968Met
XM_011542821.1:c.2794T>A	XP_011541123.1:p.Leu932Met
XM_011542824.1:c.2032T>A	XP_011541126.1:p.Leu678Met
XM_011542825.1:c.1189T>A	XP_011541127.1:p.Leu397Met
XM_011542826.1:c.1054T>A	XP_011541128.1:p.Leu352Met
XM_011542827.1:c.934T>A	XP_011541129.1:p.Leu312Met
NM_001347918.1:c.2548T>A	NP_001334847.1:p.Leu850Met
NM_001347919.1:c.2574-1001T>A	NP_001334848.1:n.2574-1001T>A
NM_001347922.1:c.997T>A	NP_001334851.1:p.Leu333Met
NM_001347923.1:c.943T>A	NP_001334852.1:p.Leu315Met
NM_001347924.1:c.688T>A	NP_001334853.1:p.Leu230Met
NM_001347925.1:c.634T>A	NP_001334854.1:p.Leu212Met
NM_001347926.1:c.714-1001T>A	NP_001334855.1:n.714-1001T>A
NM_001347927.1:c.388T>A	NP_001334856.1:p.Leu130Met
NR_144939.1:n.3301T>A
XM_011542820.2:c.2902T>A	XP_011541122.1:p.Leu968Met
XM_011542821.3:c.2794T>A	XP_011541123.1:p.Leu932Met
XM_011542824.2:c.2032T>A	XP_011541126.1:p.Leu678Met
XM_011542825.2:c.1189T>A	XP_011541127.1:p.Leu397Met
XM_011542826.2:c.1054T>A	XP_011541128.1:p.Leu352Met
XM_024448521.1:c.2914T>A	XP_024304289.1:p.Leu972Met
XR_001747870.1:n.3739T>A
XR_001747872.1:n.3085T>A
XR_001747873.1:n.3399T>A
NM_001301089.2:c.808T>A	NP_001288018.1:p.Leu270Met
NM_001347918.2:c.2548T>A	NP_001334847.2:p.Leu850Met
NM_001347919.2:c.2574-1001T>A	NP_001334848.2:n.2574-1001T>A
NM_001347920.2:c.*21064T>A	NP_001334849.2:n.*21064T>A
NM_001347922.2:c.997T>A	NP_001334851.2:p.Leu333Met
NM_001347923.2:c.943T>A	NP_001334852.2:p.Leu315Met
NM_001347924.2:c.688T>A	NP_001334853.1:p.Leu230Met
NM_001347925.2:c.634T>A	NP_001334854.1:p.Leu212Met
NM_001347926.2:c.714-1001T>A	NP_001334855.1:n.714-1001T>A
NM_001347927.2:c.388T>A	NP_001334856.1:p.Leu130Met
NM_014758.3:c.2668T>A MANE Select	NP_055573.3:p.Leu890Met
NR_144939.2:n.3293T>A