Canonical Allele Identifier: CA383457882

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750664G>C (hg19) ; chr11:g.130880769G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880769G>C , CM000673.2:g.130880769G>C	GRCh38
NC_000011.9:g.130750664G>C , CM000673.1:g.130750664G>C	GRCh37
NC_000011.8:g.130255874G>C	NCBI36
NG_053190.1:g.40720C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2611C>G MANE Select	ENSP00000265909.4:p.Gln871Glu
ENST00000265909.8:c.2611C>G	ENSP00000265909.4:p.Gln871Glu
ENST00000426933.6:c.115C>G	ENSP00000413345.2:p.Gln39Glu
ENST00000526579.5:n.178-1058C>G
ENST00000527116.5:n.373C>G
ENST00000528555.5:c.751C>G	ENSP00000435122.1:p.Gln251Glu
ENST00000530330.1:n.347C>G
ENST00000530356.5:c.751C>G	ENSP00000432307.1:p.Gln251Glu
ENST00000533318.5:n.971C>G
ENST00000534726.5:c.331C>G	ENSP00000433699.1:p.Gln111Glu
NM_001301089.1:c.751C>G	NP_001288018.1:p.Gln251Glu
NM_014758.2:c.2611C>G	NP_055573.2:p.Gln871Glu
XM_005271546.3:c.2574-1058C>G	XP_005271603.1:n.2574-1058C>G
XM_011542819.1:c.2857C>G	XP_011541121.1:p.Gln953Glu
XM_011542820.1:c.2845C>G	XP_011541122.1:p.Gln949Glu
XM_011542821.1:c.2737C>G	XP_011541123.1:p.Gln913Glu
XM_011542824.1:c.1975C>G	XP_011541126.1:p.Gln659Glu
XM_011542825.1:c.1132C>G	XP_011541127.1:p.Gln378Glu
XM_011542826.1:c.997C>G	XP_011541128.1:p.Gln333Glu
XM_011542827.1:c.877C>G	XP_011541129.1:p.Gln293Glu
NM_001347918.1:c.2491C>G	NP_001334847.1:p.Gln831Glu
NM_001347919.1:c.2574-1058C>G	NP_001334848.1:n.2574-1058C>G
NM_001347922.1:c.940C>G	NP_001334851.1:p.Gln314Glu
NM_001347923.1:c.886C>G	NP_001334852.1:p.Gln296Glu
NM_001347924.1:c.631C>G	NP_001334853.1:p.Gln211Glu
NM_001347925.1:c.577C>G	NP_001334854.1:p.Gln193Glu
NM_001347926.1:c.714-1058C>G	NP_001334855.1:n.714-1058C>G
NM_001347927.1:c.331C>G	NP_001334856.1:p.Gln111Glu
NR_144939.1:n.3244C>G
XM_011542820.2:c.2845C>G	XP_011541122.1:p.Gln949Glu
XM_011542821.3:c.2737C>G	XP_011541123.1:p.Gln913Glu
XM_011542824.2:c.1975C>G	XP_011541126.1:p.Gln659Glu
XM_011542825.2:c.1132C>G	XP_011541127.1:p.Gln378Glu
XM_011542826.2:c.997C>G	XP_011541128.1:p.Gln333Glu
XM_024448521.1:c.2857C>G	XP_024304289.1:p.Gln953Glu
XR_001747870.1:n.3682C>G
XR_001747872.1:n.3028C>G
XR_001747873.1:n.3342C>G
NM_001301089.2:c.751C>G	NP_001288018.1:p.Gln251Glu
NM_001347918.2:c.2491C>G	NP_001334847.2:p.Gln831Glu
NM_001347919.2:c.2574-1058C>G	NP_001334848.2:n.2574-1058C>G
NM_001347920.2:c.*21007C>G	NP_001334849.2:n.*21007C>G
NM_001347922.2:c.940C>G	NP_001334851.2:p.Gln314Glu
NM_001347923.2:c.886C>G	NP_001334852.2:p.Gln296Glu
NM_001347924.2:c.631C>G	NP_001334853.1:p.Gln211Glu
NM_001347925.2:c.577C>G	NP_001334854.1:p.Gln193Glu
NM_001347926.2:c.714-1058C>G	NP_001334855.1:n.714-1058C>G
NM_001347927.2:c.331C>G	NP_001334856.1:p.Gln111Glu
NM_014758.3:c.2611C>G MANE Select	NP_055573.3:p.Gln871Glu
NR_144939.2:n.3236C>G