Canonical Allele Identifier: CA383457822

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750634G>A (hg19) ; chr11:g.130880739G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880739G>A , CM000673.2:g.130880739G>A	GRCh38
NC_000011.9:g.130750634G>A , CM000673.1:g.130750634G>A	GRCh37
NC_000011.8:g.130255844G>A	NCBI36
NG_053190.1:g.40750C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2641C>T MANE Select	ENSP00000265909.4:p.Gln881Ter
ENST00000265909.8:c.2641C>T	ENSP00000265909.4:p.Gln881Ter
ENST00000426933.6:c.145C>T	ENSP00000413345.2:p.Gln49Ter
ENST00000526579.5:n.178-1028C>T
ENST00000527116.5:n.403C>T
ENST00000528555.5:c.781C>T	ENSP00000435122.1:p.Gln261Ter
ENST00000530330.1:n.377C>T
ENST00000530356.5:c.781C>T	ENSP00000432307.1:p.Gln261Ter
ENST00000533318.5:n.1001C>T
ENST00000534726.5:c.361C>T	ENSP00000433699.1:p.Gln121Ter
NM_001301089.1:c.781C>T	NP_001288018.1:p.Gln261Ter
NM_014758.2:c.2641C>T	NP_055573.2:p.Gln881Ter
XM_005271546.3:c.2574-1028C>T	XP_005271603.1:n.2574-1028C>T
XM_011542819.1:c.2887C>T	XP_011541121.1:p.Gln963Ter
XM_011542820.1:c.2875C>T	XP_011541122.1:p.Gln959Ter
XM_011542821.1:c.2767C>T	XP_011541123.1:p.Gln923Ter
XM_011542824.1:c.2005C>T	XP_011541126.1:p.Gln669Ter
XM_011542825.1:c.1162C>T	XP_011541127.1:p.Gln388Ter
XM_011542826.1:c.1027C>T	XP_011541128.1:p.Gln343Ter
XM_011542827.1:c.907C>T	XP_011541129.1:p.Gln303Ter
NM_001347918.1:c.2521C>T	NP_001334847.1:p.Gln841Ter
NM_001347919.1:c.2574-1028C>T	NP_001334848.1:n.2574-1028C>T
NM_001347922.1:c.970C>T	NP_001334851.1:p.Gln324Ter
NM_001347923.1:c.916C>T	NP_001334852.1:p.Gln306Ter
NM_001347924.1:c.661C>T	NP_001334853.1:p.Gln221Ter
NM_001347925.1:c.607C>T	NP_001334854.1:p.Gln203Ter
NM_001347926.1:c.714-1028C>T	NP_001334855.1:n.714-1028C>T
NM_001347927.1:c.361C>T	NP_001334856.1:p.Gln121Ter
NR_144939.1:n.3274C>T
XM_011542820.2:c.2875C>T	XP_011541122.1:p.Gln959Ter
XM_011542821.3:c.2767C>T	XP_011541123.1:p.Gln923Ter
XM_011542824.2:c.2005C>T	XP_011541126.1:p.Gln669Ter
XM_011542825.2:c.1162C>T	XP_011541127.1:p.Gln388Ter
XM_011542826.2:c.1027C>T	XP_011541128.1:p.Gln343Ter
XM_024448521.1:c.2887C>T	XP_024304289.1:p.Gln963Ter
XR_001747870.1:n.3712C>T
XR_001747872.1:n.3058C>T
XR_001747873.1:n.3372C>T
NM_001301089.2:c.781C>T	NP_001288018.1:p.Gln261Ter
NM_001347918.2:c.2521C>T	NP_001334847.2:p.Gln841Ter
NM_001347919.2:c.2574-1028C>T	NP_001334848.2:n.2574-1028C>T
NM_001347920.2:c.*21037C>T	NP_001334849.2:n.*21037C>T
NM_001347922.2:c.970C>T	NP_001334851.2:p.Gln324Ter
NM_001347923.2:c.916C>T	NP_001334852.2:p.Gln306Ter
NM_001347924.2:c.661C>T	NP_001334853.1:p.Gln221Ter
NM_001347925.2:c.607C>T	NP_001334854.1:p.Gln203Ter
NM_001347926.2:c.714-1028C>T	NP_001334855.1:n.714-1028C>T
NM_001347927.2:c.361C>T	NP_001334856.1:p.Gln121Ter
NM_014758.3:c.2641C>T MANE Select	NP_055573.3:p.Gln881Ter
NR_144939.2:n.3266C>T