Canonical Allele Identifier: CA383457733

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750591C>G (hg19) ; chr11:g.130880696C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880696C>G , CM000673.2:g.130880696C>G	GRCh38
NC_000011.9:g.130750591C>G , CM000673.1:g.130750591C>G	GRCh37
NC_000011.8:g.130255801C>G	NCBI36
NG_053190.1:g.40793G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2684G>C MANE Select	ENSP00000265909.4:p.Arg895Pro
ENST00000265909.8:c.2684G>C	ENSP00000265909.4:p.Arg895Pro
ENST00000426933.6:c.188G>C	ENSP00000413345.2:p.Arg63Pro
ENST00000526579.5:n.178-985G>C
ENST00000527116.5:n.446G>C
ENST00000528555.5:c.824G>C	ENSP00000435122.1:p.Arg275Pro
ENST00000530330.1:n.420G>C
ENST00000530356.5:c.824G>C	ENSP00000432307.1:p.Arg275Pro
ENST00000533318.5:n.1044G>C
ENST00000534726.5:c.404G>C	ENSP00000433699.1:p.Arg135Pro
NM_001301089.1:c.824G>C	NP_001288018.1:p.Arg275Pro
NM_014758.2:c.2684G>C	NP_055573.2:p.Arg895Pro
XM_005271546.3:c.2574-985G>C	XP_005271603.1:n.2574-985G>C
XM_011542819.1:c.2930G>C	XP_011541121.1:p.Arg977Pro
XM_011542820.1:c.2918G>C	XP_011541122.1:p.Arg973Pro
XM_011542821.1:c.2810G>C	XP_011541123.1:p.Arg937Pro
XM_011542824.1:c.2048G>C	XP_011541126.1:p.Arg683Pro
XM_011542825.1:c.1205G>C	XP_011541127.1:p.Arg402Pro
XM_011542826.1:c.1070G>C	XP_011541128.1:p.Arg357Pro
XM_011542827.1:c.950G>C	XP_011541129.1:p.Arg317Pro
NM_001347918.1:c.2564G>C	NP_001334847.1:p.Arg855Pro
NM_001347919.1:c.2574-985G>C	NP_001334848.1:n.2574-985G>C
NM_001347922.1:c.1013G>C	NP_001334851.1:p.Arg338Pro
NM_001347923.1:c.959G>C	NP_001334852.1:p.Arg320Pro
NM_001347924.1:c.704G>C	NP_001334853.1:p.Arg235Pro
NM_001347925.1:c.650G>C	NP_001334854.1:p.Arg217Pro
NM_001347926.1:c.714-985G>C	NP_001334855.1:n.714-985G>C
NM_001347927.1:c.404G>C	NP_001334856.1:p.Arg135Pro
NR_144939.1:n.3317G>C
XM_011542820.2:c.2918G>C	XP_011541122.1:p.Arg973Pro
XM_011542821.3:c.2810G>C	XP_011541123.1:p.Arg937Pro
XM_011542824.2:c.2048G>C	XP_011541126.1:p.Arg683Pro
XM_011542825.2:c.1205G>C	XP_011541127.1:p.Arg402Pro
XM_011542826.2:c.1070G>C	XP_011541128.1:p.Arg357Pro
XM_024448521.1:c.2930G>C	XP_024304289.1:p.Arg977Pro
XR_001747870.1:n.3755G>C
XR_001747872.1:n.3101G>C
XR_001747873.1:n.3415G>C
NM_001301089.2:c.824G>C	NP_001288018.1:p.Arg275Pro
NM_001347918.2:c.2564G>C	NP_001334847.2:p.Arg855Pro
NM_001347919.2:c.2574-985G>C	NP_001334848.2:n.2574-985G>C
NM_001347920.2:c.*21080G>C	NP_001334849.2:n.*21080G>C
NM_001347922.2:c.1013G>C	NP_001334851.2:p.Arg338Pro
NM_001347923.2:c.959G>C	NP_001334852.2:p.Arg320Pro
NM_001347924.2:c.704G>C	NP_001334853.1:p.Arg235Pro
NM_001347925.2:c.650G>C	NP_001334854.1:p.Arg217Pro
NM_001347926.2:c.714-985G>C	NP_001334855.1:n.714-985G>C
NM_001347927.2:c.404G>C	NP_001334856.1:p.Arg135Pro
NM_014758.3:c.2684G>C MANE Select	NP_055573.3:p.Arg895Pro
NR_144939.2:n.3309G>C