Canonical Allele Identifier: CA383457760

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750604G>T (hg19) ; chr11:g.130880709G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880709G>T , CM000673.2:g.130880709G>T	GRCh38
NC_000011.9:g.130750604G>T , CM000673.1:g.130750604G>T	GRCh37
NC_000011.8:g.130255814G>T	NCBI36
NG_053190.1:g.40780C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2671C>A MANE Select	ENSP00000265909.4:p.Pro891Thr
ENST00000265909.8:c.2671C>A	ENSP00000265909.4:p.Pro891Thr
ENST00000426933.6:c.175C>A	ENSP00000413345.2:p.Pro59Thr
ENST00000526579.5:n.178-998C>A
ENST00000527116.5:n.433C>A
ENST00000528555.5:c.811C>A	ENSP00000435122.1:p.Pro271Thr
ENST00000530330.1:n.407C>A
ENST00000530356.5:c.811C>A	ENSP00000432307.1:p.Pro271Thr
ENST00000533318.5:n.1031C>A
ENST00000534726.5:c.391C>A	ENSP00000433699.1:p.Pro131Thr
NM_001301089.1:c.811C>A	NP_001288018.1:p.Pro271Thr
NM_014758.2:c.2671C>A	NP_055573.2:p.Pro891Thr
XM_005271546.3:c.2574-998C>A	XP_005271603.1:n.2574-998C>A
XM_011542819.1:c.2917C>A	XP_011541121.1:p.Pro973Thr
XM_011542820.1:c.2905C>A	XP_011541122.1:p.Pro969Thr
XM_011542821.1:c.2797C>A	XP_011541123.1:p.Pro933Thr
XM_011542824.1:c.2035C>A	XP_011541126.1:p.Pro679Thr
XM_011542825.1:c.1192C>A	XP_011541127.1:p.Pro398Thr
XM_011542826.1:c.1057C>A	XP_011541128.1:p.Pro353Thr
XM_011542827.1:c.937C>A	XP_011541129.1:p.Pro313Thr
NM_001347918.1:c.2551C>A	NP_001334847.1:p.Pro851Thr
NM_001347919.1:c.2574-998C>A	NP_001334848.1:n.2574-998C>A
NM_001347922.1:c.1000C>A	NP_001334851.1:p.Pro334Thr
NM_001347923.1:c.946C>A	NP_001334852.1:p.Pro316Thr
NM_001347924.1:c.691C>A	NP_001334853.1:p.Pro231Thr
NM_001347925.1:c.637C>A	NP_001334854.1:p.Pro213Thr
NM_001347926.1:c.714-998C>A	NP_001334855.1:n.714-998C>A
NM_001347927.1:c.391C>A	NP_001334856.1:p.Pro131Thr
NR_144939.1:n.3304C>A
XM_011542820.2:c.2905C>A	XP_011541122.1:p.Pro969Thr
XM_011542821.3:c.2797C>A	XP_011541123.1:p.Pro933Thr
XM_011542824.2:c.2035C>A	XP_011541126.1:p.Pro679Thr
XM_011542825.2:c.1192C>A	XP_011541127.1:p.Pro398Thr
XM_011542826.2:c.1057C>A	XP_011541128.1:p.Pro353Thr
XM_024448521.1:c.2917C>A	XP_024304289.1:p.Pro973Thr
XR_001747870.1:n.3742C>A
XR_001747872.1:n.3088C>A
XR_001747873.1:n.3402C>A
NM_001301089.2:c.811C>A	NP_001288018.1:p.Pro271Thr
NM_001347918.2:c.2551C>A	NP_001334847.2:p.Pro851Thr
NM_001347919.2:c.2574-998C>A	NP_001334848.2:n.2574-998C>A
NM_001347920.2:c.*21067C>A	NP_001334849.2:n.*21067C>A
NM_001347922.2:c.1000C>A	NP_001334851.2:p.Pro334Thr
NM_001347923.2:c.946C>A	NP_001334852.2:p.Pro316Thr
NM_001347924.2:c.691C>A	NP_001334853.1:p.Pro231Thr
NM_001347925.2:c.637C>A	NP_001334854.1:p.Pro213Thr
NM_001347926.2:c.714-998C>A	NP_001334855.1:n.714-998C>A
NM_001347927.2:c.391C>A	NP_001334856.1:p.Pro131Thr
NM_014758.3:c.2671C>A MANE Select	NP_055573.3:p.Pro891Thr
NR_144939.2:n.3296C>A