Canonical Allele Identifier: CA477582304

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750611T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880716T>A , CM000673.2:g.130880716T>A	GRCh38
NC_000011.9:g.130750611T>A , CM000673.1:g.130750611T>A	GRCh37
NC_000011.8:g.130255821T>A	NCBI36
NG_053190.1:g.40773A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2664A>T MANE Select	ENSP00000265909.4:p.Gly888=
ENST00000265909.8:c.2664A>T	ENSP00000265909.4:p.Gly888=
ENST00000426933.6:c.168A>T	ENSP00000413345.2:p.Gly56=
ENST00000526579.5:n.178-1005A>T
ENST00000527116.5:n.426A>T
ENST00000528555.5:c.804A>T	ENSP00000435122.1:p.Gly268=
ENST00000530330.1:n.400A>T
ENST00000530356.5:c.804A>T	ENSP00000432307.1:p.Gly268=
ENST00000533318.5:n.1024A>T
ENST00000534726.5:c.384A>T	ENSP00000433699.1:p.Gly128=
NM_001301089.1:c.804A>T	NP_001288018.1:p.Gly268=
NM_014758.2:c.2664A>T	NP_055573.2:p.Gly888=
XM_005271546.3:c.2574-1005A>T	XP_005271603.1:n.2574-1005A>T
XM_011542819.1:c.2910A>T	XP_011541121.1:p.Gly970=
XM_011542820.1:c.2898A>T	XP_011541122.1:p.Gly966=
XM_011542821.1:c.2790A>T	XP_011541123.1:p.Gly930=
XM_011542824.1:c.2028A>T	XP_011541126.1:p.Gly676=
XM_011542825.1:c.1185A>T	XP_011541127.1:p.Gly395=
XM_011542826.1:c.1050A>T	XP_011541128.1:p.Gly350=
XM_011542827.1:c.930A>T	XP_011541129.1:p.Gly310=
NM_001347918.1:c.2544A>T	NP_001334847.1:p.Gly848=
NM_001347919.1:c.2574-1005A>T	NP_001334848.1:n.2574-1005A>T
NM_001347922.1:c.993A>T	NP_001334851.1:p.Gly331=
NM_001347923.1:c.939A>T	NP_001334852.1:p.Gly313=
NM_001347924.1:c.684A>T	NP_001334853.1:p.Gly228=
NM_001347925.1:c.630A>T	NP_001334854.1:p.Gly210=
NM_001347926.1:c.714-1005A>T	NP_001334855.1:n.714-1005A>T
NM_001347927.1:c.384A>T	NP_001334856.1:p.Gly128=
NR_144939.1:n.3297A>T
XM_011542820.2:c.2898A>T	XP_011541122.1:p.Gly966=
XM_011542821.3:c.2790A>T	XP_011541123.1:p.Gly930=
XM_011542824.2:c.2028A>T	XP_011541126.1:p.Gly676=
XM_011542825.2:c.1185A>T	XP_011541127.1:p.Gly395=
XM_011542826.2:c.1050A>T	XP_011541128.1:p.Gly350=
XM_024448521.1:c.2910A>T	XP_024304289.1:p.Gly970=
XR_001747870.1:n.3735A>T
XR_001747872.1:n.3081A>T
XR_001747873.1:n.3395A>T
NM_001301089.2:c.804A>T	NP_001288018.1:p.Gly268=
NM_001347918.2:c.2544A>T	NP_001334847.2:p.Gly848=
NM_001347919.2:c.2574-1005A>T	NP_001334848.2:n.2574-1005A>T
NM_001347920.2:c.*21060A>T	NP_001334849.2:n.*21060A>T
NM_001347922.2:c.993A>T	NP_001334851.2:p.Gly331=
NM_001347923.2:c.939A>T	NP_001334852.2:p.Gly313=
NM_001347924.2:c.684A>T	NP_001334853.1:p.Gly228=
NM_001347925.2:c.630A>T	NP_001334854.1:p.Gly210=
NM_001347926.2:c.714-1005A>T	NP_001334855.1:n.714-1005A>T
NM_001347927.2:c.384A>T	NP_001334856.1:p.Gly128=
NM_014758.3:c.2664A>T MANE Select	NP_055573.3:p.Gly888=
NR_144939.2:n.3289A>T