Canonical Allele Identifier: CA6366588

Gene: SNX19

Linked Data

• dbSNP Id: rs759986844
• ExAC: 11:130750638 A / C
• gnomAD v2: 11-130750638-A-C
• gnomAD v4: 11-130880743-A-C
• MyVariant Identifiers: chr11:g.130750638A>C (hg19) ; chr11:g.130880743A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880743A>C , CM000673.2:g.130880743A>C	GRCh38
NC_000011.9:g.130750638A>C , CM000673.1:g.130750638A>C	GRCh37
NC_000011.8:g.130255848A>C	NCBI36
NG_053190.1:g.40746T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2637T>G MANE Select	ENSP00000265909.4:p.Leu879=
ENST00000265909.8:c.2637T>G	ENSP00000265909.4:p.Leu879=
ENST00000426933.6:c.141T>G	ENSP00000413345.2:p.Leu47=
ENST00000526579.5:n.178-1032T>G
ENST00000527116.5:n.399T>G
ENST00000528555.5:c.777T>G	ENSP00000435122.1:p.Leu259=
ENST00000530330.1:n.373T>G
ENST00000530356.5:c.777T>G	ENSP00000432307.1:p.Leu259=
ENST00000533318.5:n.997T>G
ENST00000534726.5:c.357T>G	ENSP00000433699.1:p.Leu119=
NM_001301089.1:c.777T>G	NP_001288018.1:p.Leu259=
NM_014758.2:c.2637T>G	NP_055573.2:p.Leu879=
XM_005271546.3:c.2574-1032T>G	XP_005271603.1:n.2574-1032T>G
XM_011542819.1:c.2883T>G	XP_011541121.1:p.Leu961=
XM_011542820.1:c.2871T>G	XP_011541122.1:p.Leu957=
XM_011542821.1:c.2763T>G	XP_011541123.1:p.Leu921=
XM_011542824.1:c.2001T>G	XP_011541126.1:p.Leu667=
XM_011542825.1:c.1158T>G	XP_011541127.1:p.Leu386=
XM_011542826.1:c.1023T>G	XP_011541128.1:p.Leu341=
XM_011542827.1:c.903T>G	XP_011541129.1:p.Leu301=
NM_001347918.1:c.2517T>G	NP_001334847.1:p.Leu839=
NM_001347919.1:c.2574-1032T>G	NP_001334848.1:n.2574-1032T>G
NM_001347922.1:c.966T>G	NP_001334851.1:p.Leu322=
NM_001347923.1:c.912T>G	NP_001334852.1:p.Leu304=
NM_001347924.1:c.657T>G	NP_001334853.1:p.Leu219=
NM_001347925.1:c.603T>G	NP_001334854.1:p.Leu201=
NM_001347926.1:c.714-1032T>G	NP_001334855.1:n.714-1032T>G
NM_001347927.1:c.357T>G	NP_001334856.1:p.Leu119=
NR_144939.1:n.3270T>G
XM_011542820.2:c.2871T>G	XP_011541122.1:p.Leu957=
XM_011542821.3:c.2763T>G	XP_011541123.1:p.Leu921=
XM_011542824.2:c.2001T>G	XP_011541126.1:p.Leu667=
XM_011542825.2:c.1158T>G	XP_011541127.1:p.Leu386=
XM_011542826.2:c.1023T>G	XP_011541128.1:p.Leu341=
XM_024448521.1:c.2883T>G	XP_024304289.1:p.Leu961=
XR_001747870.1:n.3708T>G
XR_001747872.1:n.3054T>G
XR_001747873.1:n.3368T>G
NM_001301089.2:c.777T>G	NP_001288018.1:p.Leu259=
NM_001347918.2:c.2517T>G	NP_001334847.2:p.Leu839=
NM_001347919.2:c.2574-1032T>G	NP_001334848.2:n.2574-1032T>G
NM_001347920.2:c.*21033T>G	NP_001334849.2:n.*21033T>G
NM_001347922.2:c.966T>G	NP_001334851.2:p.Leu322=
NM_001347923.2:c.912T>G	NP_001334852.2:p.Leu304=
NM_001347924.2:c.657T>G	NP_001334853.1:p.Leu219=
NM_001347925.2:c.603T>G	NP_001334854.1:p.Leu201=
NM_001347926.2:c.714-1032T>G	NP_001334855.1:n.714-1032T>G
NM_001347927.2:c.357T>G	NP_001334856.1:p.Leu119=
NM_014758.3:c.2637T>G MANE Select	NP_055573.3:p.Leu879=
NR_144939.2:n.3262T>G