Canonical Allele Identifier: CA2616844394

Gene: SNX19

Linked Data

• gnomAD v4: 11-130880745-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880746dup , CM000673.2:g.130880746dup	GRCh38
NC_000011.9:g.130750641dup , CM000673.1:g.130750641dup	GRCh37
NC_000011.8:g.130255851dup	NCBI36
NG_053190.1:g.40743dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2634dup MANE Select	ENSP00000265909.4:p.Leu879AlafsTer14
ENST00000265909.8:c.2634dup	ENSP00000265909.4:p.Leu879AlafsTer14
ENST00000426933.6:c.138dup	ENSP00000413345.2:p.Leu47AlafsTer14
ENST00000526579.5:n.178-1035dup
ENST00000527116.5:n.396dup
ENST00000528555.5:c.774dup	ENSP00000435122.1:p.Leu259AlafsTer14
ENST00000530330.1:n.370dup
ENST00000530356.5:c.774dup	ENSP00000432307.1:p.Leu259AlafsTer14
ENST00000533318.5:n.994dup
ENST00000534726.5:c.354dup	ENSP00000433699.1:p.Leu119AlafsTer14
NM_001301089.1:c.774dup	NP_001288018.1:p.Leu259AlafsTer14
NM_014758.2:c.2634dup	NP_055573.2:p.Leu879AlafsTer14
XM_005271546.3:c.2574-1035dup	XP_005271603.1:n.2574-1035dup
XM_011542819.1:c.2880dup	XP_011541121.1:p.Leu961AlafsTer14
XM_011542820.1:c.2868dup	XP_011541122.1:p.Leu957AlafsTer14
XM_011542821.1:c.2760dup	XP_011541123.1:p.Leu921AlafsTer14
XM_011542824.1:c.1998dup	XP_011541126.1:p.Leu667AlafsTer14
XM_011542825.1:c.1155dup	XP_011541127.1:p.Leu386AlafsTer14
XM_011542826.1:c.1020dup	XP_011541128.1:p.Leu341AlafsTer14
XM_011542827.1:c.900dup	XP_011541129.1:p.Leu301AlafsTer14
NM_001347918.1:c.2514dup	NP_001334847.1:p.Leu839AlafsTer14
NM_001347919.1:c.2574-1035dup	NP_001334848.1:n.2574-1035dup
NM_001347922.1:c.963dup	NP_001334851.1:p.Leu322AlafsTer14
NM_001347923.1:c.909dup	NP_001334852.1:p.Leu304AlafsTer14
NM_001347924.1:c.654dup	NP_001334853.1:p.Leu219AlafsTer14
NM_001347925.1:c.600dup	NP_001334854.1:p.Leu201AlafsTer14
NM_001347926.1:c.714-1035dup	NP_001334855.1:n.714-1035dup
NM_001347927.1:c.354dup	NP_001334856.1:p.Leu119AlafsTer14
NR_144939.1:n.3267dup
XM_011542820.2:c.2868dup	XP_011541122.1:p.Leu957AlafsTer14
XM_011542821.3:c.2760dup	XP_011541123.1:p.Leu921AlafsTer14
XM_011542824.2:c.1998dup	XP_011541126.1:p.Leu667AlafsTer14
XM_011542825.2:c.1155dup	XP_011541127.1:p.Leu386AlafsTer14
XM_011542826.2:c.1020dup	XP_011541128.1:p.Leu341AlafsTer14
XM_024448521.1:c.2880dup	XP_024304289.1:p.Leu961AlafsTer14
XR_001747870.1:n.3705dup
XR_001747872.1:n.3051dup
XR_001747873.1:n.3365dup
NM_001301089.2:c.774dup	NP_001288018.1:p.Leu259AlafsTer14
NM_001347918.2:c.2514dup	NP_001334847.2:p.Leu839AlafsTer14
NM_001347919.2:c.2574-1035dup	NP_001334848.2:n.2574-1035dup
NM_001347920.2:c.*21030dup	NP_001334849.2:n.*21030dup
NM_001347922.2:c.963dup	NP_001334851.2:p.Leu322AlafsTer14
NM_001347923.2:c.909dup	NP_001334852.2:p.Leu304AlafsTer14
NM_001347924.2:c.654dup	NP_001334853.1:p.Leu219AlafsTer14
NM_001347925.2:c.600dup	NP_001334854.1:p.Leu201AlafsTer14
NM_001347926.2:c.714-1035dup	NP_001334855.1:n.714-1035dup
NM_001347927.2:c.354dup	NP_001334856.1:p.Leu119AlafsTer14
NM_014758.3:c.2634dup MANE Select	NP_055573.3:p.Leu879AlafsTer14
NR_144939.2:n.3259dup