Canonical Allele Identifier: CA383457681

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750567T>A (hg19) ; chr11:g.130880672T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880672T>A , CM000673.2:g.130880672T>A	GRCh38
NC_000011.9:g.130750567T>A , CM000673.1:g.130750567T>A	GRCh37
NC_000011.8:g.130255777T>A	NCBI36
NG_053190.1:g.40817A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2708A>T MANE Select	ENSP00000265909.4:p.Lys903Ile
ENST00000265909.8:c.2708A>T	ENSP00000265909.4:p.Lys903Ile
ENST00000426933.6:c.212A>T	ENSP00000413345.2:p.Lys71Ile
ENST00000526579.5:n.178-961A>T
ENST00000527116.5:n.470A>T
ENST00000528555.5:c.848A>T	ENSP00000435122.1:p.Lys283Ile
ENST00000530330.1:n.444A>T
ENST00000530356.5:c.848A>T	ENSP00000432307.1:p.Lys283Ile
ENST00000533318.5:n.1068A>T
ENST00000534726.5:c.428A>T	ENSP00000433699.1:p.Lys143Ile
NM_001301089.1:c.848A>T	NP_001288018.1:p.Lys283Ile
NM_014758.2:c.2708A>T	NP_055573.2:p.Lys903Ile
XM_005271546.3:c.2574-961A>T	XP_005271603.1:n.2574-961A>T
XM_011542819.1:c.2954A>T	XP_011541121.1:p.Lys985Ile
XM_011542820.1:c.2942A>T	XP_011541122.1:p.Lys981Ile
XM_011542821.1:c.2834A>T	XP_011541123.1:p.Lys945Ile
XM_011542824.1:c.2072A>T	XP_011541126.1:p.Lys691Ile
XM_011542825.1:c.1229A>T	XP_011541127.1:p.Lys410Ile
XM_011542826.1:c.1094A>T	XP_011541128.1:p.Lys365Ile
XM_011542827.1:c.974A>T	XP_011541129.1:p.Lys325Ile
NM_001347918.1:c.2588A>T	NP_001334847.1:p.Lys863Ile
NM_001347919.1:c.2574-961A>T	NP_001334848.1:n.2574-961A>T
NM_001347922.1:c.1037A>T	NP_001334851.1:p.Lys346Ile
NM_001347923.1:c.983A>T	NP_001334852.1:p.Lys328Ile
NM_001347924.1:c.728A>T	NP_001334853.1:p.Lys243Ile
NM_001347925.1:c.674A>T	NP_001334854.1:p.Lys225Ile
NM_001347926.1:c.714-961A>T	NP_001334855.1:n.714-961A>T
NM_001347927.1:c.428A>T	NP_001334856.1:p.Lys143Ile
NR_144939.1:n.3341A>T
XM_011542820.2:c.2942A>T	XP_011541122.1:p.Lys981Ile
XM_011542821.3:c.2834A>T	XP_011541123.1:p.Lys945Ile
XM_011542824.2:c.2072A>T	XP_011541126.1:p.Lys691Ile
XM_011542825.2:c.1229A>T	XP_011541127.1:p.Lys410Ile
XM_011542826.2:c.1094A>T	XP_011541128.1:p.Lys365Ile
XM_024448521.1:c.2954A>T	XP_024304289.1:p.Lys985Ile
XR_001747870.1:n.3779A>T
XR_001747872.1:n.3125A>T
XR_001747873.1:n.3439A>T
NM_001301089.2:c.848A>T	NP_001288018.1:p.Lys283Ile
NM_001347918.2:c.2588A>T	NP_001334847.2:p.Lys863Ile
NM_001347919.2:c.2574-961A>T	NP_001334848.2:n.2574-961A>T
NM_001347920.2:c.*21104A>T	NP_001334849.2:n.*21104A>T
NM_001347922.2:c.1037A>T	NP_001334851.2:p.Lys346Ile
NM_001347923.2:c.983A>T	NP_001334852.2:p.Lys328Ile
NM_001347924.2:c.728A>T	NP_001334853.1:p.Lys243Ile
NM_001347925.2:c.674A>T	NP_001334854.1:p.Lys225Ile
NM_001347926.2:c.714-961A>T	NP_001334855.1:n.714-961A>T
NM_001347927.2:c.428A>T	NP_001334856.1:p.Lys143Ile
NM_014758.3:c.2708A>T MANE Select	NP_055573.3:p.Lys903Ile
NR_144939.2:n.3333A>T