Canonical Allele Identifier: CA383457696

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750573T>A (hg19) ; chr11:g.130880678T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880678T>A , CM000673.2:g.130880678T>A	GRCh38
NC_000011.9:g.130750573T>A , CM000673.1:g.130750573T>A	GRCh37
NC_000011.8:g.130255783T>A	NCBI36
NG_053190.1:g.40811A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2702A>T MANE Select	ENSP00000265909.4:p.Glu901Val
ENST00000265909.8:c.2702A>T	ENSP00000265909.4:p.Glu901Val
ENST00000426933.6:c.206A>T	ENSP00000413345.2:p.Glu69Val
ENST00000526579.5:n.178-967A>T
ENST00000527116.5:n.464A>T
ENST00000528555.5:c.842A>T	ENSP00000435122.1:p.Glu281Val
ENST00000530330.1:n.438A>T
ENST00000530356.5:c.842A>T	ENSP00000432307.1:p.Glu281Val
ENST00000533318.5:n.1062A>T
ENST00000534726.5:c.422A>T	ENSP00000433699.1:p.Glu141Val
NM_001301089.1:c.842A>T	NP_001288018.1:p.Glu281Val
NM_014758.2:c.2702A>T	NP_055573.2:p.Glu901Val
XM_005271546.3:c.2574-967A>T	XP_005271603.1:n.2574-967A>T
XM_011542819.1:c.2948A>T	XP_011541121.1:p.Glu983Val
XM_011542820.1:c.2936A>T	XP_011541122.1:p.Glu979Val
XM_011542821.1:c.2828A>T	XP_011541123.1:p.Glu943Val
XM_011542824.1:c.2066A>T	XP_011541126.1:p.Glu689Val
XM_011542825.1:c.1223A>T	XP_011541127.1:p.Glu408Val
XM_011542826.1:c.1088A>T	XP_011541128.1:p.Glu363Val
XM_011542827.1:c.968A>T	XP_011541129.1:p.Glu323Val
NM_001347918.1:c.2582A>T	NP_001334847.1:p.Glu861Val
NM_001347919.1:c.2574-967A>T	NP_001334848.1:n.2574-967A>T
NM_001347922.1:c.1031A>T	NP_001334851.1:p.Glu344Val
NM_001347923.1:c.977A>T	NP_001334852.1:p.Glu326Val
NM_001347924.1:c.722A>T	NP_001334853.1:p.Glu241Val
NM_001347925.1:c.668A>T	NP_001334854.1:p.Glu223Val
NM_001347926.1:c.714-967A>T	NP_001334855.1:n.714-967A>T
NM_001347927.1:c.422A>T	NP_001334856.1:p.Glu141Val
NR_144939.1:n.3335A>T
XM_011542820.2:c.2936A>T	XP_011541122.1:p.Glu979Val
XM_011542821.3:c.2828A>T	XP_011541123.1:p.Glu943Val
XM_011542824.2:c.2066A>T	XP_011541126.1:p.Glu689Val
XM_011542825.2:c.1223A>T	XP_011541127.1:p.Glu408Val
XM_011542826.2:c.1088A>T	XP_011541128.1:p.Glu363Val
XM_024448521.1:c.2948A>T	XP_024304289.1:p.Glu983Val
XR_001747870.1:n.3773A>T
XR_001747872.1:n.3119A>T
XR_001747873.1:n.3433A>T
NM_001301089.2:c.842A>T	NP_001288018.1:p.Glu281Val
NM_001347918.2:c.2582A>T	NP_001334847.2:p.Glu861Val
NM_001347919.2:c.2574-967A>T	NP_001334848.2:n.2574-967A>T
NM_001347920.2:c.*21098A>T	NP_001334849.2:n.*21098A>T
NM_001347922.2:c.1031A>T	NP_001334851.2:p.Glu344Val
NM_001347923.2:c.977A>T	NP_001334852.2:p.Glu326Val
NM_001347924.2:c.722A>T	NP_001334853.1:p.Glu241Val
NM_001347925.2:c.668A>T	NP_001334854.1:p.Glu223Val
NM_001347926.2:c.714-967A>T	NP_001334855.1:n.714-967A>T
NM_001347927.2:c.422A>T	NP_001334856.1:p.Glu141Val
NM_014758.3:c.2702A>T MANE Select	NP_055573.3:p.Glu901Val
NR_144939.2:n.3327A>T