Canonical Allele Identifier: CA383457868

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750657C>G (hg19) ; chr11:g.130880762C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880762C>G , CM000673.2:g.130880762C>G	GRCh38
NC_000011.9:g.130750657C>G , CM000673.1:g.130750657C>G	GRCh37
NC_000011.8:g.130255867C>G	NCBI36
NG_053190.1:g.40727G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2618G>C MANE Select	ENSP00000265909.4:p.Trp873Ser
ENST00000265909.8:c.2618G>C	ENSP00000265909.4:p.Trp873Ser
ENST00000426933.6:c.122G>C	ENSP00000413345.2:p.Trp41Ser
ENST00000526579.5:n.178-1051G>C
ENST00000527116.5:n.380G>C
ENST00000528555.5:c.758G>C	ENSP00000435122.1:p.Trp253Ser
ENST00000530330.1:n.354G>C
ENST00000530356.5:c.758G>C	ENSP00000432307.1:p.Trp253Ser
ENST00000533318.5:n.978G>C
ENST00000534726.5:c.338G>C	ENSP00000433699.1:p.Trp113Ser
NM_001301089.1:c.758G>C	NP_001288018.1:p.Trp253Ser
NM_014758.2:c.2618G>C	NP_055573.2:p.Trp873Ser
XM_005271546.3:c.2574-1051G>C	XP_005271603.1:n.2574-1051G>C
XM_011542819.1:c.2864G>C	XP_011541121.1:p.Trp955Ser
XM_011542820.1:c.2852G>C	XP_011541122.1:p.Trp951Ser
XM_011542821.1:c.2744G>C	XP_011541123.1:p.Trp915Ser
XM_011542824.1:c.1982G>C	XP_011541126.1:p.Trp661Ser
XM_011542825.1:c.1139G>C	XP_011541127.1:p.Trp380Ser
XM_011542826.1:c.1004G>C	XP_011541128.1:p.Trp335Ser
XM_011542827.1:c.884G>C	XP_011541129.1:p.Trp295Ser
NM_001347918.1:c.2498G>C	NP_001334847.1:p.Trp833Ser
NM_001347919.1:c.2574-1051G>C	NP_001334848.1:n.2574-1051G>C
NM_001347922.1:c.947G>C	NP_001334851.1:p.Trp316Ser
NM_001347923.1:c.893G>C	NP_001334852.1:p.Trp298Ser
NM_001347924.1:c.638G>C	NP_001334853.1:p.Trp213Ser
NM_001347925.1:c.584G>C	NP_001334854.1:p.Trp195Ser
NM_001347926.1:c.714-1051G>C	NP_001334855.1:n.714-1051G>C
NM_001347927.1:c.338G>C	NP_001334856.1:p.Trp113Ser
NR_144939.1:n.3251G>C
XM_011542820.2:c.2852G>C	XP_011541122.1:p.Trp951Ser
XM_011542821.3:c.2744G>C	XP_011541123.1:p.Trp915Ser
XM_011542824.2:c.1982G>C	XP_011541126.1:p.Trp661Ser
XM_011542825.2:c.1139G>C	XP_011541127.1:p.Trp380Ser
XM_011542826.2:c.1004G>C	XP_011541128.1:p.Trp335Ser
XM_024448521.1:c.2864G>C	XP_024304289.1:p.Trp955Ser
XR_001747870.1:n.3689G>C
XR_001747872.1:n.3035G>C
XR_001747873.1:n.3349G>C
NM_001301089.2:c.758G>C	NP_001288018.1:p.Trp253Ser
NM_001347918.2:c.2498G>C	NP_001334847.2:p.Trp833Ser
NM_001347919.2:c.2574-1051G>C	NP_001334848.2:n.2574-1051G>C
NM_001347920.2:c.*21014G>C	NP_001334849.2:n.*21014G>C
NM_001347922.2:c.947G>C	NP_001334851.2:p.Trp316Ser
NM_001347923.2:c.893G>C	NP_001334852.2:p.Trp298Ser
NM_001347924.2:c.638G>C	NP_001334853.1:p.Trp213Ser
NM_001347925.2:c.584G>C	NP_001334854.1:p.Trp195Ser
NM_001347926.2:c.714-1051G>C	NP_001334855.1:n.714-1051G>C
NM_001347927.2:c.338G>C	NP_001334856.1:p.Trp113Ser
NM_014758.3:c.2618G>C MANE Select	NP_055573.3:p.Trp873Ser
NR_144939.2:n.3243G>C