Canonical Allele Identifier: CA383457879

Gene: SNX19

Linked Data

• gnomAD v4: 11-130880768-T-C
• MyVariant Identifiers: chr11:g.130750663T>C (hg19) ; chr11:g.130880768T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880768T>C , CM000673.2:g.130880768T>C	GRCh38
NC_000011.9:g.130750663T>C , CM000673.1:g.130750663T>C	GRCh37
NC_000011.8:g.130255873T>C	NCBI36
NG_053190.1:g.40721A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2612A>G MANE Select	ENSP00000265909.4:p.Gln871Arg
ENST00000265909.8:c.2612A>G	ENSP00000265909.4:p.Gln871Arg
ENST00000426933.6:c.116A>G	ENSP00000413345.2:p.Gln39Arg
ENST00000526579.5:n.178-1057A>G
ENST00000527116.5:n.374A>G
ENST00000528555.5:c.752A>G	ENSP00000435122.1:p.Gln251Arg
ENST00000530330.1:n.348A>G
ENST00000530356.5:c.752A>G	ENSP00000432307.1:p.Gln251Arg
ENST00000533318.5:n.972A>G
ENST00000534726.5:c.332A>G	ENSP00000433699.1:p.Gln111Arg
NM_001301089.1:c.752A>G	NP_001288018.1:p.Gln251Arg
NM_014758.2:c.2612A>G	NP_055573.2:p.Gln871Arg
XM_005271546.3:c.2574-1057A>G	XP_005271603.1:n.2574-1057A>G
XM_011542819.1:c.2858A>G	XP_011541121.1:p.Gln953Arg
XM_011542820.1:c.2846A>G	XP_011541122.1:p.Gln949Arg
XM_011542821.1:c.2738A>G	XP_011541123.1:p.Gln913Arg
XM_011542824.1:c.1976A>G	XP_011541126.1:p.Gln659Arg
XM_011542825.1:c.1133A>G	XP_011541127.1:p.Gln378Arg
XM_011542826.1:c.998A>G	XP_011541128.1:p.Gln333Arg
XM_011542827.1:c.878A>G	XP_011541129.1:p.Gln293Arg
NM_001347918.1:c.2492A>G	NP_001334847.1:p.Gln831Arg
NM_001347919.1:c.2574-1057A>G	NP_001334848.1:n.2574-1057A>G
NM_001347922.1:c.941A>G	NP_001334851.1:p.Gln314Arg
NM_001347923.1:c.887A>G	NP_001334852.1:p.Gln296Arg
NM_001347924.1:c.632A>G	NP_001334853.1:p.Gln211Arg
NM_001347925.1:c.578A>G	NP_001334854.1:p.Gln193Arg
NM_001347926.1:c.714-1057A>G	NP_001334855.1:n.714-1057A>G
NM_001347927.1:c.332A>G	NP_001334856.1:p.Gln111Arg
NR_144939.1:n.3245A>G
XM_011542820.2:c.2846A>G	XP_011541122.1:p.Gln949Arg
XM_011542821.3:c.2738A>G	XP_011541123.1:p.Gln913Arg
XM_011542824.2:c.1976A>G	XP_011541126.1:p.Gln659Arg
XM_011542825.2:c.1133A>G	XP_011541127.1:p.Gln378Arg
XM_011542826.2:c.998A>G	XP_011541128.1:p.Gln333Arg
XM_024448521.1:c.2858A>G	XP_024304289.1:p.Gln953Arg
XR_001747870.1:n.3683A>G
XR_001747872.1:n.3029A>G
XR_001747873.1:n.3343A>G
NM_001301089.2:c.752A>G	NP_001288018.1:p.Gln251Arg
NM_001347918.2:c.2492A>G	NP_001334847.2:p.Gln831Arg
NM_001347919.2:c.2574-1057A>G	NP_001334848.2:n.2574-1057A>G
NM_001347920.2:c.*21008A>G	NP_001334849.2:n.*21008A>G
NM_001347922.2:c.941A>G	NP_001334851.2:p.Gln314Arg
NM_001347923.2:c.887A>G	NP_001334852.2:p.Gln296Arg
NM_001347924.2:c.632A>G	NP_001334853.1:p.Gln211Arg
NM_001347925.2:c.578A>G	NP_001334854.1:p.Gln193Arg
NM_001347926.2:c.714-1057A>G	NP_001334855.1:n.714-1057A>G
NM_001347927.2:c.332A>G	NP_001334856.1:p.Gln111Arg
NM_014758.3:c.2612A>G MANE Select	NP_055573.3:p.Gln871Arg
NR_144939.2:n.3237A>G