Canonical Allele Identifier: CA477582280

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750583T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880688T>G , CM000673.2:g.130880688T>G	GRCh38
NC_000011.9:g.130750583T>G , CM000673.1:g.130750583T>G	GRCh37
NC_000011.8:g.130255793T>G	NCBI36
NG_053190.1:g.40801A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2692A>C MANE Select	ENSP00000265909.4:p.Arg898=
ENST00000265909.8:c.2692A>C	ENSP00000265909.4:p.Arg898=
ENST00000426933.6:c.196A>C	ENSP00000413345.2:p.Arg66=
ENST00000526579.5:n.178-977A>C
ENST00000527116.5:n.454A>C
ENST00000528555.5:c.832A>C	ENSP00000435122.1:p.Arg278=
ENST00000530330.1:n.428A>C
ENST00000530356.5:c.832A>C	ENSP00000432307.1:p.Arg278=
ENST00000533318.5:n.1052A>C
ENST00000534726.5:c.412A>C	ENSP00000433699.1:p.Arg138=
NM_001301089.1:c.832A>C	NP_001288018.1:p.Arg278=
NM_014758.2:c.2692A>C	NP_055573.2:p.Arg898=
XM_005271546.3:c.2574-977A>C	XP_005271603.1:n.2574-977A>C
XM_011542819.1:c.2938A>C	XP_011541121.1:p.Arg980=
XM_011542820.1:c.2926A>C	XP_011541122.1:p.Arg976=
XM_011542821.1:c.2818A>C	XP_011541123.1:p.Arg940=
XM_011542824.1:c.2056A>C	XP_011541126.1:p.Arg686=
XM_011542825.1:c.1213A>C	XP_011541127.1:p.Arg405=
XM_011542826.1:c.1078A>C	XP_011541128.1:p.Arg360=
XM_011542827.1:c.958A>C	XP_011541129.1:p.Arg320=
NM_001347918.1:c.2572A>C	NP_001334847.1:p.Arg858=
NM_001347919.1:c.2574-977A>C	NP_001334848.1:n.2574-977A>C
NM_001347922.1:c.1021A>C	NP_001334851.1:p.Arg341=
NM_001347923.1:c.967A>C	NP_001334852.1:p.Arg323=
NM_001347924.1:c.712A>C	NP_001334853.1:p.Arg238=
NM_001347925.1:c.658A>C	NP_001334854.1:p.Arg220=
NM_001347926.1:c.714-977A>C	NP_001334855.1:n.714-977A>C
NM_001347927.1:c.412A>C	NP_001334856.1:p.Arg138=
NR_144939.1:n.3325A>C
XM_011542820.2:c.2926A>C	XP_011541122.1:p.Arg976=
XM_011542821.3:c.2818A>C	XP_011541123.1:p.Arg940=
XM_011542824.2:c.2056A>C	XP_011541126.1:p.Arg686=
XM_011542825.2:c.1213A>C	XP_011541127.1:p.Arg405=
XM_011542826.2:c.1078A>C	XP_011541128.1:p.Arg360=
XM_024448521.1:c.2938A>C	XP_024304289.1:p.Arg980=
XR_001747870.1:n.3763A>C
XR_001747872.1:n.3109A>C
XR_001747873.1:n.3423A>C
NM_001301089.2:c.832A>C	NP_001288018.1:p.Arg278=
NM_001347918.2:c.2572A>C	NP_001334847.2:p.Arg858=
NM_001347919.2:c.2574-977A>C	NP_001334848.2:n.2574-977A>C
NM_001347920.2:c.*21088A>C	NP_001334849.2:n.*21088A>C
NM_001347922.2:c.1021A>C	NP_001334851.2:p.Arg341=
NM_001347923.2:c.967A>C	NP_001334852.2:p.Arg323=
NM_001347924.2:c.712A>C	NP_001334853.1:p.Arg238=
NM_001347925.2:c.658A>C	NP_001334854.1:p.Arg220=
NM_001347926.2:c.714-977A>C	NP_001334855.1:n.714-977A>C
NM_001347927.2:c.412A>C	NP_001334856.1:p.Arg138=
NM_014758.3:c.2692A>C MANE Select	NP_055573.3:p.Arg898=
NR_144939.2:n.3317A>C