Canonical Allele Identifier: CA383457710

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750579G>A (hg19) ; chr11:g.130880684G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880684G>A , CM000673.2:g.130880684G>A	GRCh38
NC_000011.9:g.130750579G>A , CM000673.1:g.130750579G>A	GRCh37
NC_000011.8:g.130255789G>A	NCBI36
NG_053190.1:g.40805C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2696C>T MANE Select	ENSP00000265909.4:p.Thr899Ile
ENST00000265909.8:c.2696C>T	ENSP00000265909.4:p.Thr899Ile
ENST00000426933.6:c.200C>T	ENSP00000413345.2:p.Thr67Ile
ENST00000526579.5:n.178-973C>T
ENST00000527116.5:n.458C>T
ENST00000528555.5:c.836C>T	ENSP00000435122.1:p.Thr279Ile
ENST00000530330.1:n.432C>T
ENST00000530356.5:c.836C>T	ENSP00000432307.1:p.Thr279Ile
ENST00000533318.5:n.1056C>T
ENST00000534726.5:c.416C>T	ENSP00000433699.1:p.Thr139Ile
NM_001301089.1:c.836C>T	NP_001288018.1:p.Thr279Ile
NM_014758.2:c.2696C>T	NP_055573.2:p.Thr899Ile
XM_005271546.3:c.2574-973C>T	XP_005271603.1:n.2574-973C>T
XM_011542819.1:c.2942C>T	XP_011541121.1:p.Thr981Ile
XM_011542820.1:c.2930C>T	XP_011541122.1:p.Thr977Ile
XM_011542821.1:c.2822C>T	XP_011541123.1:p.Thr941Ile
XM_011542824.1:c.2060C>T	XP_011541126.1:p.Thr687Ile
XM_011542825.1:c.1217C>T	XP_011541127.1:p.Thr406Ile
XM_011542826.1:c.1082C>T	XP_011541128.1:p.Thr361Ile
XM_011542827.1:c.962C>T	XP_011541129.1:p.Thr321Ile
NM_001347918.1:c.2576C>T	NP_001334847.1:p.Thr859Ile
NM_001347919.1:c.2574-973C>T	NP_001334848.1:n.2574-973C>T
NM_001347922.1:c.1025C>T	NP_001334851.1:p.Thr342Ile
NM_001347923.1:c.971C>T	NP_001334852.1:p.Thr324Ile
NM_001347924.1:c.716C>T	NP_001334853.1:p.Thr239Ile
NM_001347925.1:c.662C>T	NP_001334854.1:p.Thr221Ile
NM_001347926.1:c.714-973C>T	NP_001334855.1:n.714-973C>T
NM_001347927.1:c.416C>T	NP_001334856.1:p.Thr139Ile
NR_144939.1:n.3329C>T
XM_011542820.2:c.2930C>T	XP_011541122.1:p.Thr977Ile
XM_011542821.3:c.2822C>T	XP_011541123.1:p.Thr941Ile
XM_011542824.2:c.2060C>T	XP_011541126.1:p.Thr687Ile
XM_011542825.2:c.1217C>T	XP_011541127.1:p.Thr406Ile
XM_011542826.2:c.1082C>T	XP_011541128.1:p.Thr361Ile
XM_024448521.1:c.2942C>T	XP_024304289.1:p.Thr981Ile
XR_001747870.1:n.3767C>T
XR_001747872.1:n.3113C>T
XR_001747873.1:n.3427C>T
NM_001301089.2:c.836C>T	NP_001288018.1:p.Thr279Ile
NM_001347918.2:c.2576C>T	NP_001334847.2:p.Thr859Ile
NM_001347919.2:c.2574-973C>T	NP_001334848.2:n.2574-973C>T
NM_001347920.2:c.*21092C>T	NP_001334849.2:n.*21092C>T
NM_001347922.2:c.1025C>T	NP_001334851.2:p.Thr342Ile
NM_001347923.2:c.971C>T	NP_001334852.2:p.Thr324Ile
NM_001347924.2:c.716C>T	NP_001334853.1:p.Thr239Ile
NM_001347925.2:c.662C>T	NP_001334854.1:p.Thr221Ile
NM_001347926.2:c.714-973C>T	NP_001334855.1:n.714-973C>T
NM_001347927.2:c.416C>T	NP_001334856.1:p.Thr139Ile
NM_014758.3:c.2696C>T MANE Select	NP_055573.3:p.Thr899Ile
NR_144939.2:n.3321C>T