Canonical Allele Identifier: CA383457646

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750550G>C (hg19) ; chr11:g.130880655G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880655G>C , CM000673.2:g.130880655G>C	GRCh38
NC_000011.9:g.130750550G>C , CM000673.1:g.130750550G>C	GRCh37
NC_000011.8:g.130255760G>C	NCBI36
NG_053190.1:g.40834C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2725C>G MANE Select	ENSP00000265909.4:p.Gln909Glu
ENST00000265909.8:c.2725C>G	ENSP00000265909.4:p.Gln909Glu
ENST00000426933.6:c.229C>G	ENSP00000413345.2:p.Gln77Glu
ENST00000526579.5:n.178-944C>G
ENST00000527116.5:n.487C>G
ENST00000528555.5:c.865C>G	ENSP00000435122.1:p.Gln289Glu
ENST00000530330.1:n.461C>G
ENST00000530356.5:c.865C>G	ENSP00000432307.1:p.Gln289Glu
ENST00000533318.5:n.1085C>G
ENST00000534726.5:c.445C>G	ENSP00000433699.1:p.Gln149Glu
NM_001301089.1:c.865C>G	NP_001288018.1:p.Gln289Glu
NM_014758.2:c.2725C>G	NP_055573.2:p.Gln909Glu
XM_005271546.3:c.2574-944C>G	XP_005271603.1:n.2574-944C>G
XM_011542819.1:c.2971C>G	XP_011541121.1:p.Gln991Glu
XM_011542820.1:c.2959C>G	XP_011541122.1:p.Gln987Glu
XM_011542821.1:c.2851C>G	XP_011541123.1:p.Gln951Glu
XM_011542824.1:c.2089C>G	XP_011541126.1:p.Gln697Glu
XM_011542825.1:c.1246C>G	XP_011541127.1:p.Gln416Glu
XM_011542826.1:c.1111C>G	XP_011541128.1:p.Gln371Glu
XM_011542827.1:c.991C>G	XP_011541129.1:p.Gln331Glu
NM_001347918.1:c.2605C>G	NP_001334847.1:p.Gln869Glu
NM_001347919.1:c.2574-944C>G	NP_001334848.1:n.2574-944C>G
NM_001347922.1:c.1054C>G	NP_001334851.1:p.Gln352Glu
NM_001347923.1:c.1000C>G	NP_001334852.1:p.Gln334Glu
NM_001347924.1:c.745C>G	NP_001334853.1:p.Gln249Glu
NM_001347925.1:c.691C>G	NP_001334854.1:p.Gln231Glu
NM_001347926.1:c.714-944C>G	NP_001334855.1:n.714-944C>G
NM_001347927.1:c.445C>G	NP_001334856.1:p.Gln149Glu
NR_144939.1:n.3358C>G
XM_011542820.2:c.2959C>G	XP_011541122.1:p.Gln987Glu
XM_011542821.3:c.2851C>G	XP_011541123.1:p.Gln951Glu
XM_011542824.2:c.2089C>G	XP_011541126.1:p.Gln697Glu
XM_011542825.2:c.1246C>G	XP_011541127.1:p.Gln416Glu
XM_011542826.2:c.1111C>G	XP_011541128.1:p.Gln371Glu
XM_024448521.1:c.2971C>G	XP_024304289.1:p.Gln991Glu
XR_001747870.1:n.3796C>G
XR_001747872.1:n.3142C>G
XR_001747873.1:n.3456C>G
NM_001301089.2:c.865C>G	NP_001288018.1:p.Gln289Glu
NM_001347918.2:c.2605C>G	NP_001334847.2:p.Gln869Glu
NM_001347919.2:c.2574-944C>G	NP_001334848.2:n.2574-944C>G
NM_001347920.2:c.*21121C>G	NP_001334849.2:n.*21121C>G
NM_001347922.2:c.1054C>G	NP_001334851.2:p.Gln352Glu
NM_001347923.2:c.1000C>G	NP_001334852.2:p.Gln334Glu
NM_001347924.2:c.745C>G	NP_001334853.1:p.Gln249Glu
NM_001347925.2:c.691C>G	NP_001334854.1:p.Gln231Glu
NM_001347926.2:c.714-944C>G	NP_001334855.1:n.714-944C>G
NM_001347927.2:c.445C>G	NP_001334856.1:p.Gln149Glu
NM_014758.3:c.2725C>G MANE Select	NP_055573.3:p.Gln909Glu
NR_144939.2:n.3350C>G