Canonical Allele Identifier: CA383457823

Gene: SNX19

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2641C>G MANE Select	ENSP00000265909.4:p.Gln881Glu
ENST00000265909.8:c.2641C>G	ENSP00000265909.4:p.Gln881Glu
ENST00000426933.6:c.145C>G	ENSP00000413345.2:p.Gln49Glu
ENST00000526579.5:n.178-1028C>G
ENST00000527116.5:n.403C>G
ENST00000528555.5:c.781C>G	ENSP00000435122.1:p.Gln261Glu
ENST00000530330.1:n.377C>G
ENST00000530356.5:c.781C>G	ENSP00000432307.1:p.Gln261Glu
ENST00000533318.5:n.1001C>G
ENST00000534726.5:c.361C>G	ENSP00000433699.1:p.Gln121Glu
NM_001301089.1:c.781C>G	NP_001288018.1:p.Gln261Glu
NM_014758.2:c.2641C>G	NP_055573.2:p.Gln881Glu
XM_005271546.3:c.2574-1028C>G	XP_005271603.1:n.2574-1028C>G
XM_011542819.1:c.2887C>G	XP_011541121.1:p.Gln963Glu
XM_011542820.1:c.2875C>G	XP_011541122.1:p.Gln959Glu
XM_011542821.1:c.2767C>G	XP_011541123.1:p.Gln923Glu
XM_011542824.1:c.2005C>G	XP_011541126.1:p.Gln669Glu
XM_011542825.1:c.1162C>G	XP_011541127.1:p.Gln388Glu
XM_011542826.1:c.1027C>G	XP_011541128.1:p.Gln343Glu
XM_011542827.1:c.907C>G	XP_011541129.1:p.Gln303Glu
NM_001347918.1:c.2521C>G	NP_001334847.1:p.Gln841Glu
NM_001347919.1:c.2574-1028C>G	NP_001334848.1:n.2574-1028C>G
NM_001347922.1:c.970C>G	NP_001334851.1:p.Gln324Glu
NM_001347923.1:c.916C>G	NP_001334852.1:p.Gln306Glu
NM_001347924.1:c.661C>G	NP_001334853.1:p.Gln221Glu
NM_001347925.1:c.607C>G	NP_001334854.1:p.Gln203Glu
NM_001347926.1:c.714-1028C>G	NP_001334855.1:n.714-1028C>G
NM_001347927.1:c.361C>G	NP_001334856.1:p.Gln121Glu
NR_144939.1:n.3274C>G
XM_011542820.2:c.2875C>G	XP_011541122.1:p.Gln959Glu
XM_011542821.3:c.2767C>G	XP_011541123.1:p.Gln923Glu
XM_011542824.2:c.2005C>G	XP_011541126.1:p.Gln669Glu
XM_011542825.2:c.1162C>G	XP_011541127.1:p.Gln388Glu
XM_011542826.2:c.1027C>G	XP_011541128.1:p.Gln343Glu
XM_024448521.1:c.2887C>G	XP_024304289.1:p.Gln963Glu
XR_001747870.1:n.3712C>G
XR_001747872.1:n.3058C>G
XR_001747873.1:n.3372C>G
NM_001301089.2:c.781C>G	NP_001288018.1:p.Gln261Glu
NM_001347918.2:c.2521C>G	NP_001334847.2:p.Gln841Glu
NM_001347919.2:c.2574-1028C>G	NP_001334848.2:n.2574-1028C>G
NM_001347920.2:c.*21037C>G	NP_001334849.2:n.*21037C>G
NM_001347922.2:c.970C>G	NP_001334851.2:p.Gln324Glu
NM_001347923.2:c.916C>G	NP_001334852.2:p.Gln306Glu
NM_001347924.2:c.661C>G	NP_001334853.1:p.Gln221Glu
NM_001347925.2:c.607C>G	NP_001334854.1:p.Gln203Glu
NM_001347926.2:c.714-1028C>G	NP_001334855.1:n.714-1028C>G
NM_001347927.2:c.361C>G	NP_001334856.1:p.Gln121Glu
NM_014758.3:c.2641C>G MANE Select	NP_055573.3:p.Gln881Glu
NR_144939.2:n.3266C>G