Canonical Allele Identifier: CA383457672

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750562C>T (hg19) ; chr11:g.130880667C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880667C>T , CM000673.2:g.130880667C>T	GRCh38
NC_000011.9:g.130750562C>T , CM000673.1:g.130750562C>T	GRCh37
NC_000011.8:g.130255772C>T	NCBI36
NG_053190.1:g.40822G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2713G>A MANE Select	ENSP00000265909.4:p.Ala905Thr
ENST00000265909.8:c.2713G>A	ENSP00000265909.4:p.Ala905Thr
ENST00000426933.6:c.217G>A	ENSP00000413345.2:p.Ala73Thr
ENST00000526579.5:n.178-956G>A
ENST00000527116.5:n.475G>A
ENST00000528555.5:c.853G>A	ENSP00000435122.1:p.Ala285Thr
ENST00000530330.1:n.449G>A
ENST00000530356.5:c.853G>A	ENSP00000432307.1:p.Ala285Thr
ENST00000533318.5:n.1073G>A
ENST00000534726.5:c.433G>A	ENSP00000433699.1:p.Ala145Thr
NM_001301089.1:c.853G>A	NP_001288018.1:p.Ala285Thr
NM_014758.2:c.2713G>A	NP_055573.2:p.Ala905Thr
XM_005271546.3:c.2574-956G>A	XP_005271603.1:n.2574-956G>A
XM_011542819.1:c.2959G>A	XP_011541121.1:p.Ala987Thr
XM_011542820.1:c.2947G>A	XP_011541122.1:p.Ala983Thr
XM_011542821.1:c.2839G>A	XP_011541123.1:p.Ala947Thr
XM_011542824.1:c.2077G>A	XP_011541126.1:p.Ala693Thr
XM_011542825.1:c.1234G>A	XP_011541127.1:p.Ala412Thr
XM_011542826.1:c.1099G>A	XP_011541128.1:p.Ala367Thr
XM_011542827.1:c.979G>A	XP_011541129.1:p.Ala327Thr
NM_001347918.1:c.2593G>A	NP_001334847.1:p.Ala865Thr
NM_001347919.1:c.2574-956G>A	NP_001334848.1:n.2574-956G>A
NM_001347922.1:c.1042G>A	NP_001334851.1:p.Ala348Thr
NM_001347923.1:c.988G>A	NP_001334852.1:p.Ala330Thr
NM_001347924.1:c.733G>A	NP_001334853.1:p.Ala245Thr
NM_001347925.1:c.679G>A	NP_001334854.1:p.Ala227Thr
NM_001347926.1:c.714-956G>A	NP_001334855.1:n.714-956G>A
NM_001347927.1:c.433G>A	NP_001334856.1:p.Ala145Thr
NR_144939.1:n.3346G>A
XM_011542820.2:c.2947G>A	XP_011541122.1:p.Ala983Thr
XM_011542821.3:c.2839G>A	XP_011541123.1:p.Ala947Thr
XM_011542824.2:c.2077G>A	XP_011541126.1:p.Ala693Thr
XM_011542825.2:c.1234G>A	XP_011541127.1:p.Ala412Thr
XM_011542826.2:c.1099G>A	XP_011541128.1:p.Ala367Thr
XM_024448521.1:c.2959G>A	XP_024304289.1:p.Ala987Thr
XR_001747870.1:n.3784G>A
XR_001747872.1:n.3130G>A
XR_001747873.1:n.3444G>A
NM_001301089.2:c.853G>A	NP_001288018.1:p.Ala285Thr
NM_001347918.2:c.2593G>A	NP_001334847.2:p.Ala865Thr
NM_001347919.2:c.2574-956G>A	NP_001334848.2:n.2574-956G>A
NM_001347920.2:c.*21109G>A	NP_001334849.2:n.*21109G>A
NM_001347922.2:c.1042G>A	NP_001334851.2:p.Ala348Thr
NM_001347923.2:c.988G>A	NP_001334852.2:p.Ala330Thr
NM_001347924.2:c.733G>A	NP_001334853.1:p.Ala245Thr
NM_001347925.2:c.679G>A	NP_001334854.1:p.Ala227Thr
NM_001347926.2:c.714-956G>A	NP_001334855.1:n.714-956G>A
NM_001347927.2:c.433G>A	NP_001334856.1:p.Ala145Thr
NM_014758.3:c.2713G>A MANE Select	NP_055573.3:p.Ala905Thr
NR_144939.2:n.3338G>A