Canonical Allele Identifier: CA383457718

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750582C>T (hg19) ; chr11:g.130880687C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880687C>T , CM000673.2:g.130880687C>T	GRCh38
NC_000011.9:g.130750582C>T , CM000673.1:g.130750582C>T	GRCh37
NC_000011.8:g.130255792C>T	NCBI36
NG_053190.1:g.40802G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2693G>A MANE Select	ENSP00000265909.4:p.Arg898Lys
ENST00000265909.8:c.2693G>A	ENSP00000265909.4:p.Arg898Lys
ENST00000426933.6:c.197G>A	ENSP00000413345.2:p.Arg66Lys
ENST00000526579.5:n.178-976G>A
ENST00000527116.5:n.455G>A
ENST00000528555.5:c.833G>A	ENSP00000435122.1:p.Arg278Lys
ENST00000530330.1:n.429G>A
ENST00000530356.5:c.833G>A	ENSP00000432307.1:p.Arg278Lys
ENST00000533318.5:n.1053G>A
ENST00000534726.5:c.413G>A	ENSP00000433699.1:p.Arg138Lys
NM_001301089.1:c.833G>A	NP_001288018.1:p.Arg278Lys
NM_014758.2:c.2693G>A	NP_055573.2:p.Arg898Lys
XM_005271546.3:c.2574-976G>A	XP_005271603.1:n.2574-976G>A
XM_011542819.1:c.2939G>A	XP_011541121.1:p.Arg980Lys
XM_011542820.1:c.2927G>A	XP_011541122.1:p.Arg976Lys
XM_011542821.1:c.2819G>A	XP_011541123.1:p.Arg940Lys
XM_011542824.1:c.2057G>A	XP_011541126.1:p.Arg686Lys
XM_011542825.1:c.1214G>A	XP_011541127.1:p.Arg405Lys
XM_011542826.1:c.1079G>A	XP_011541128.1:p.Arg360Lys
XM_011542827.1:c.959G>A	XP_011541129.1:p.Arg320Lys
NM_001347918.1:c.2573G>A	NP_001334847.1:p.Arg858Lys
NM_001347919.1:c.2574-976G>A	NP_001334848.1:n.2574-976G>A
NM_001347922.1:c.1022G>A	NP_001334851.1:p.Arg341Lys
NM_001347923.1:c.968G>A	NP_001334852.1:p.Arg323Lys
NM_001347924.1:c.713G>A	NP_001334853.1:p.Arg238Lys
NM_001347925.1:c.659G>A	NP_001334854.1:p.Arg220Lys
NM_001347926.1:c.714-976G>A	NP_001334855.1:n.714-976G>A
NM_001347927.1:c.413G>A	NP_001334856.1:p.Arg138Lys
NR_144939.1:n.3326G>A
XM_011542820.2:c.2927G>A	XP_011541122.1:p.Arg976Lys
XM_011542821.3:c.2819G>A	XP_011541123.1:p.Arg940Lys
XM_011542824.2:c.2057G>A	XP_011541126.1:p.Arg686Lys
XM_011542825.2:c.1214G>A	XP_011541127.1:p.Arg405Lys
XM_011542826.2:c.1079G>A	XP_011541128.1:p.Arg360Lys
XM_024448521.1:c.2939G>A	XP_024304289.1:p.Arg980Lys
XR_001747870.1:n.3764G>A
XR_001747872.1:n.3110G>A
XR_001747873.1:n.3424G>A
NM_001301089.2:c.833G>A	NP_001288018.1:p.Arg278Lys
NM_001347918.2:c.2573G>A	NP_001334847.2:p.Arg858Lys
NM_001347919.2:c.2574-976G>A	NP_001334848.2:n.2574-976G>A
NM_001347920.2:c.*21089G>A	NP_001334849.2:n.*21089G>A
NM_001347922.2:c.1022G>A	NP_001334851.2:p.Arg341Lys
NM_001347923.2:c.968G>A	NP_001334852.2:p.Arg323Lys
NM_001347924.2:c.713G>A	NP_001334853.1:p.Arg238Lys
NM_001347925.2:c.659G>A	NP_001334854.1:p.Arg220Lys
NM_001347926.2:c.714-976G>A	NP_001334855.1:n.714-976G>A
NM_001347927.2:c.413G>A	NP_001334856.1:p.Arg138Lys
NM_014758.3:c.2693G>A MANE Select	NP_055573.3:p.Arg898Lys
NR_144939.2:n.3318G>A