Canonical Allele Identifier: CA477582301

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750608A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880713A>C , CM000673.2:g.130880713A>C	GRCh38
NC_000011.9:g.130750608A>C , CM000673.1:g.130750608A>C	GRCh37
NC_000011.8:g.130255818A>C	NCBI36
NG_053190.1:g.40776T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2667T>G MANE Select	ENSP00000265909.4:p.Val889=
ENST00000265909.8:c.2667T>G	ENSP00000265909.4:p.Val889=
ENST00000426933.6:c.171T>G	ENSP00000413345.2:p.Val57=
ENST00000526579.5:n.178-1002T>G
ENST00000527116.5:n.429T>G
ENST00000528555.5:c.807T>G	ENSP00000435122.1:p.Val269=
ENST00000530330.1:n.403T>G
ENST00000530356.5:c.807T>G	ENSP00000432307.1:p.Val269=
ENST00000533318.5:n.1027T>G
ENST00000534726.5:c.387T>G	ENSP00000433699.1:p.Val129=
NM_001301089.1:c.807T>G	NP_001288018.1:p.Val269=
NM_014758.2:c.2667T>G	NP_055573.2:p.Val889=
XM_005271546.3:c.2574-1002T>G	XP_005271603.1:n.2574-1002T>G
XM_011542819.1:c.2913T>G	XP_011541121.1:p.Val971=
XM_011542820.1:c.2901T>G	XP_011541122.1:p.Val967=
XM_011542821.1:c.2793T>G	XP_011541123.1:p.Val931=
XM_011542824.1:c.2031T>G	XP_011541126.1:p.Val677=
XM_011542825.1:c.1188T>G	XP_011541127.1:p.Val396=
XM_011542826.1:c.1053T>G	XP_011541128.1:p.Val351=
XM_011542827.1:c.933T>G	XP_011541129.1:p.Val311=
NM_001347918.1:c.2547T>G	NP_001334847.1:p.Val849=
NM_001347919.1:c.2574-1002T>G	NP_001334848.1:n.2574-1002T>G
NM_001347922.1:c.996T>G	NP_001334851.1:p.Val332=
NM_001347923.1:c.942T>G	NP_001334852.1:p.Val314=
NM_001347924.1:c.687T>G	NP_001334853.1:p.Val229=
NM_001347925.1:c.633T>G	NP_001334854.1:p.Val211=
NM_001347926.1:c.714-1002T>G	NP_001334855.1:n.714-1002T>G
NM_001347927.1:c.387T>G	NP_001334856.1:p.Val129=
NR_144939.1:n.3300T>G
XM_011542820.2:c.2901T>G	XP_011541122.1:p.Val967=
XM_011542821.3:c.2793T>G	XP_011541123.1:p.Val931=
XM_011542824.2:c.2031T>G	XP_011541126.1:p.Val677=
XM_011542825.2:c.1188T>G	XP_011541127.1:p.Val396=
XM_011542826.2:c.1053T>G	XP_011541128.1:p.Val351=
XM_024448521.1:c.2913T>G	XP_024304289.1:p.Val971=
XR_001747870.1:n.3738T>G
XR_001747872.1:n.3084T>G
XR_001747873.1:n.3398T>G
NM_001301089.2:c.807T>G	NP_001288018.1:p.Val269=
NM_001347918.2:c.2547T>G	NP_001334847.2:p.Val849=
NM_001347919.2:c.2574-1002T>G	NP_001334848.2:n.2574-1002T>G
NM_001347920.2:c.*21063T>G	NP_001334849.2:n.*21063T>G
NM_001347922.2:c.996T>G	NP_001334851.2:p.Val332=
NM_001347923.2:c.942T>G	NP_001334852.2:p.Val314=
NM_001347924.2:c.687T>G	NP_001334853.1:p.Val229=
NM_001347925.2:c.633T>G	NP_001334854.1:p.Val211=
NM_001347926.2:c.714-1002T>G	NP_001334855.1:n.714-1002T>G
NM_001347927.2:c.387T>G	NP_001334856.1:p.Val129=
NM_014758.3:c.2667T>G MANE Select	NP_055573.3:p.Val889=
NR_144939.2:n.3292T>G