Canonical Allele Identifier: CA383457866

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750656C>G (hg19) ; chr11:g.130880761C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880761C>G , CM000673.2:g.130880761C>G	GRCh38
NC_000011.9:g.130750656C>G , CM000673.1:g.130750656C>G	GRCh37
NC_000011.8:g.130255866C>G	NCBI36
NG_053190.1:g.40728G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2619G>C MANE Select	ENSP00000265909.4:p.Trp873Cys
ENST00000265909.8:c.2619G>C	ENSP00000265909.4:p.Trp873Cys
ENST00000426933.6:c.123G>C	ENSP00000413345.2:p.Trp41Cys
ENST00000526579.5:n.178-1050G>C
ENST00000527116.5:n.381G>C
ENST00000528555.5:c.759G>C	ENSP00000435122.1:p.Trp253Cys
ENST00000530330.1:n.355G>C
ENST00000530356.5:c.759G>C	ENSP00000432307.1:p.Trp253Cys
ENST00000533318.5:n.979G>C
ENST00000534726.5:c.339G>C	ENSP00000433699.1:p.Trp113Cys
NM_001301089.1:c.759G>C	NP_001288018.1:p.Trp253Cys
NM_014758.2:c.2619G>C	NP_055573.2:p.Trp873Cys
XM_005271546.3:c.2574-1050G>C	XP_005271603.1:n.2574-1050G>C
XM_011542819.1:c.2865G>C	XP_011541121.1:p.Trp955Cys
XM_011542820.1:c.2853G>C	XP_011541122.1:p.Trp951Cys
XM_011542821.1:c.2745G>C	XP_011541123.1:p.Trp915Cys
XM_011542824.1:c.1983G>C	XP_011541126.1:p.Trp661Cys
XM_011542825.1:c.1140G>C	XP_011541127.1:p.Trp380Cys
XM_011542826.1:c.1005G>C	XP_011541128.1:p.Trp335Cys
XM_011542827.1:c.885G>C	XP_011541129.1:p.Trp295Cys
NM_001347918.1:c.2499G>C	NP_001334847.1:p.Trp833Cys
NM_001347919.1:c.2574-1050G>C	NP_001334848.1:n.2574-1050G>C
NM_001347922.1:c.948G>C	NP_001334851.1:p.Trp316Cys
NM_001347923.1:c.894G>C	NP_001334852.1:p.Trp298Cys
NM_001347924.1:c.639G>C	NP_001334853.1:p.Trp213Cys
NM_001347925.1:c.585G>C	NP_001334854.1:p.Trp195Cys
NM_001347926.1:c.714-1050G>C	NP_001334855.1:n.714-1050G>C
NM_001347927.1:c.339G>C	NP_001334856.1:p.Trp113Cys
NR_144939.1:n.3252G>C
XM_011542820.2:c.2853G>C	XP_011541122.1:p.Trp951Cys
XM_011542821.3:c.2745G>C	XP_011541123.1:p.Trp915Cys
XM_011542824.2:c.1983G>C	XP_011541126.1:p.Trp661Cys
XM_011542825.2:c.1140G>C	XP_011541127.1:p.Trp380Cys
XM_011542826.2:c.1005G>C	XP_011541128.1:p.Trp335Cys
XM_024448521.1:c.2865G>C	XP_024304289.1:p.Trp955Cys
XR_001747870.1:n.3690G>C
XR_001747872.1:n.3036G>C
XR_001747873.1:n.3350G>C
NM_001301089.2:c.759G>C	NP_001288018.1:p.Trp253Cys
NM_001347918.2:c.2499G>C	NP_001334847.2:p.Trp833Cys
NM_001347919.2:c.2574-1050G>C	NP_001334848.2:n.2574-1050G>C
NM_001347920.2:c.*21015G>C	NP_001334849.2:n.*21015G>C
NM_001347922.2:c.948G>C	NP_001334851.2:p.Trp316Cys
NM_001347923.2:c.894G>C	NP_001334852.2:p.Trp298Cys
NM_001347924.2:c.639G>C	NP_001334853.1:p.Trp213Cys
NM_001347925.2:c.585G>C	NP_001334854.1:p.Trp195Cys
NM_001347926.2:c.714-1050G>C	NP_001334855.1:n.714-1050G>C
NM_001347927.2:c.339G>C	NP_001334856.1:p.Trp113Cys
NM_014758.3:c.2619G>C MANE Select	NP_055573.3:p.Trp873Cys
NR_144939.2:n.3244G>C