Canonical Allele Identifier: CA383457778

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750613C>G (hg19) ; chr11:g.130880718C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880718C>G , CM000673.2:g.130880718C>G	GRCh38
NC_000011.9:g.130750613C>G , CM000673.1:g.130750613C>G	GRCh37
NC_000011.8:g.130255823C>G	NCBI36
NG_053190.1:g.40771G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2662G>C MANE Select	ENSP00000265909.4:p.Gly888Arg
ENST00000265909.8:c.2662G>C	ENSP00000265909.4:p.Gly888Arg
ENST00000426933.6:c.166G>C	ENSP00000413345.2:p.Gly56Arg
ENST00000526579.5:n.178-1007G>C
ENST00000527116.5:n.424G>C
ENST00000528555.5:c.802G>C	ENSP00000435122.1:p.Gly268Arg
ENST00000530330.1:n.398G>C
ENST00000530356.5:c.802G>C	ENSP00000432307.1:p.Gly268Arg
ENST00000533318.5:n.1022G>C
ENST00000534726.5:c.382G>C	ENSP00000433699.1:p.Gly128Arg
NM_001301089.1:c.802G>C	NP_001288018.1:p.Gly268Arg
NM_014758.2:c.2662G>C	NP_055573.2:p.Gly888Arg
XM_005271546.3:c.2574-1007G>C	XP_005271603.1:n.2574-1007G>C
XM_011542819.1:c.2908G>C	XP_011541121.1:p.Gly970Arg
XM_011542820.1:c.2896G>C	XP_011541122.1:p.Gly966Arg
XM_011542821.1:c.2788G>C	XP_011541123.1:p.Gly930Arg
XM_011542824.1:c.2026G>C	XP_011541126.1:p.Gly676Arg
XM_011542825.1:c.1183G>C	XP_011541127.1:p.Gly395Arg
XM_011542826.1:c.1048G>C	XP_011541128.1:p.Gly350Arg
XM_011542827.1:c.928G>C	XP_011541129.1:p.Gly310Arg
NM_001347918.1:c.2542G>C	NP_001334847.1:p.Gly848Arg
NM_001347919.1:c.2574-1007G>C	NP_001334848.1:n.2574-1007G>C
NM_001347922.1:c.991G>C	NP_001334851.1:p.Gly331Arg
NM_001347923.1:c.937G>C	NP_001334852.1:p.Gly313Arg
NM_001347924.1:c.682G>C	NP_001334853.1:p.Gly228Arg
NM_001347925.1:c.628G>C	NP_001334854.1:p.Gly210Arg
NM_001347926.1:c.714-1007G>C	NP_001334855.1:n.714-1007G>C
NM_001347927.1:c.382G>C	NP_001334856.1:p.Gly128Arg
NR_144939.1:n.3295G>C
XM_011542820.2:c.2896G>C	XP_011541122.1:p.Gly966Arg
XM_011542821.3:c.2788G>C	XP_011541123.1:p.Gly930Arg
XM_011542824.2:c.2026G>C	XP_011541126.1:p.Gly676Arg
XM_011542825.2:c.1183G>C	XP_011541127.1:p.Gly395Arg
XM_011542826.2:c.1048G>C	XP_011541128.1:p.Gly350Arg
XM_024448521.1:c.2908G>C	XP_024304289.1:p.Gly970Arg
XR_001747870.1:n.3733G>C
XR_001747872.1:n.3079G>C
XR_001747873.1:n.3393G>C
NM_001301089.2:c.802G>C	NP_001288018.1:p.Gly268Arg
NM_001347918.2:c.2542G>C	NP_001334847.2:p.Gly848Arg
NM_001347919.2:c.2574-1007G>C	NP_001334848.2:n.2574-1007G>C
NM_001347920.2:c.*21058G>C	NP_001334849.2:n.*21058G>C
NM_001347922.2:c.991G>C	NP_001334851.2:p.Gly331Arg
NM_001347923.2:c.937G>C	NP_001334852.2:p.Gly313Arg
NM_001347924.2:c.682G>C	NP_001334853.1:p.Gly228Arg
NM_001347925.2:c.628G>C	NP_001334854.1:p.Gly210Arg
NM_001347926.2:c.714-1007G>C	NP_001334855.1:n.714-1007G>C
NM_001347927.2:c.382G>C	NP_001334856.1:p.Gly128Arg
NM_014758.3:c.2662G>C MANE Select	NP_055573.3:p.Gly888Arg
NR_144939.2:n.3287G>C