Canonical Allele Identifier: CA6366580

Gene: SNX19

Linked Data

• dbSNP Id: rs775294079
• ExAC: 11:130750597 A / G
• gnomAD v2: 11-130750597-A-G
• gnomAD v4: 11-130880702-A-G
• MyVariant Identifiers: chr11:g.130750597A>G (hg19) ; chr11:g.130880702A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880702A>G , CM000673.2:g.130880702A>G	GRCh38
NC_000011.9:g.130750597A>G , CM000673.1:g.130750597A>G	GRCh37
NC_000011.8:g.130255807A>G	NCBI36
NG_053190.1:g.40787T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2678T>C MANE Select	ENSP00000265909.4:p.Phe893Ser
ENST00000265909.8:c.2678T>C	ENSP00000265909.4:p.Phe893Ser
ENST00000426933.6:c.182T>C	ENSP00000413345.2:p.Phe61Ser
ENST00000526579.5:n.178-991T>C
ENST00000527116.5:n.440T>C
ENST00000528555.5:c.818T>C	ENSP00000435122.1:p.Phe273Ser
ENST00000530330.1:n.414T>C
ENST00000530356.5:c.818T>C	ENSP00000432307.1:p.Phe273Ser
ENST00000533318.5:n.1038T>C
ENST00000534726.5:c.398T>C	ENSP00000433699.1:p.Phe133Ser
NM_001301089.1:c.818T>C	NP_001288018.1:p.Phe273Ser
NM_014758.2:c.2678T>C	NP_055573.2:p.Phe893Ser
XM_005271546.3:c.2574-991T>C	XP_005271603.1:n.2574-991T>C
XM_011542819.1:c.2924T>C	XP_011541121.1:p.Phe975Ser
XM_011542820.1:c.2912T>C	XP_011541122.1:p.Phe971Ser
XM_011542821.1:c.2804T>C	XP_011541123.1:p.Phe935Ser
XM_011542824.1:c.2042T>C	XP_011541126.1:p.Phe681Ser
XM_011542825.1:c.1199T>C	XP_011541127.1:p.Phe400Ser
XM_011542826.1:c.1064T>C	XP_011541128.1:p.Phe355Ser
XM_011542827.1:c.944T>C	XP_011541129.1:p.Phe315Ser
NM_001347918.1:c.2558T>C	NP_001334847.1:p.Phe853Ser
NM_001347919.1:c.2574-991T>C	NP_001334848.1:n.2574-991T>C
NM_001347922.1:c.1007T>C	NP_001334851.1:p.Phe336Ser
NM_001347923.1:c.953T>C	NP_001334852.1:p.Phe318Ser
NM_001347924.1:c.698T>C	NP_001334853.1:p.Phe233Ser
NM_001347925.1:c.644T>C	NP_001334854.1:p.Phe215Ser
NM_001347926.1:c.714-991T>C	NP_001334855.1:n.714-991T>C
NM_001347927.1:c.398T>C	NP_001334856.1:p.Phe133Ser
NR_144939.1:n.3311T>C
XM_011542820.2:c.2912T>C	XP_011541122.1:p.Phe971Ser
XM_011542821.3:c.2804T>C	XP_011541123.1:p.Phe935Ser
XM_011542824.2:c.2042T>C	XP_011541126.1:p.Phe681Ser
XM_011542825.2:c.1199T>C	XP_011541127.1:p.Phe400Ser
XM_011542826.2:c.1064T>C	XP_011541128.1:p.Phe355Ser
XM_024448521.1:c.2924T>C	XP_024304289.1:p.Phe975Ser
XR_001747870.1:n.3749T>C
XR_001747872.1:n.3095T>C
XR_001747873.1:n.3409T>C
NM_001301089.2:c.818T>C	NP_001288018.1:p.Phe273Ser
NM_001347918.2:c.2558T>C	NP_001334847.2:p.Phe853Ser
NM_001347919.2:c.2574-991T>C	NP_001334848.2:n.2574-991T>C
NM_001347920.2:c.*21074T>C	NP_001334849.2:n.*21074T>C
NM_001347922.2:c.1007T>C	NP_001334851.2:p.Phe336Ser
NM_001347923.2:c.953T>C	NP_001334852.2:p.Phe318Ser
NM_001347924.2:c.698T>C	NP_001334853.1:p.Phe233Ser
NM_001347925.2:c.644T>C	NP_001334854.1:p.Phe215Ser
NM_001347926.2:c.714-991T>C	NP_001334855.1:n.714-991T>C
NM_001347927.2:c.398T>C	NP_001334856.1:p.Phe133Ser
NM_014758.3:c.2678T>C MANE Select	NP_055573.3:p.Phe893Ser
NR_144939.2:n.3303T>C