Canonical Allele Identifier: CA383457827

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750636A>T (hg19) ; chr11:g.130880741A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880741A>T , CM000673.2:g.130880741A>T	GRCh38
NC_000011.9:g.130750636A>T , CM000673.1:g.130750636A>T	GRCh37
NC_000011.8:g.130255846A>T	NCBI36
NG_053190.1:g.40748T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2639T>A MANE Select	ENSP00000265909.4:p.Leu880His
ENST00000265909.8:c.2639T>A	ENSP00000265909.4:p.Leu880His
ENST00000426933.6:c.143T>A	ENSP00000413345.2:p.Leu48His
ENST00000526579.5:n.178-1030T>A
ENST00000527116.5:n.401T>A
ENST00000528555.5:c.779T>A	ENSP00000435122.1:p.Leu260His
ENST00000530330.1:n.375T>A
ENST00000530356.5:c.779T>A	ENSP00000432307.1:p.Leu260His
ENST00000533318.5:n.999T>A
ENST00000534726.5:c.359T>A	ENSP00000433699.1:p.Leu120His
NM_001301089.1:c.779T>A	NP_001288018.1:p.Leu260His
NM_014758.2:c.2639T>A	NP_055573.2:p.Leu880His
XM_005271546.3:c.2574-1030T>A	XP_005271603.1:n.2574-1030T>A
XM_011542819.1:c.2885T>A	XP_011541121.1:p.Leu962His
XM_011542820.1:c.2873T>A	XP_011541122.1:p.Leu958His
XM_011542821.1:c.2765T>A	XP_011541123.1:p.Leu922His
XM_011542824.1:c.2003T>A	XP_011541126.1:p.Leu668His
XM_011542825.1:c.1160T>A	XP_011541127.1:p.Leu387His
XM_011542826.1:c.1025T>A	XP_011541128.1:p.Leu342His
XM_011542827.1:c.905T>A	XP_011541129.1:p.Leu302His
NM_001347918.1:c.2519T>A	NP_001334847.1:p.Leu840His
NM_001347919.1:c.2574-1030T>A	NP_001334848.1:n.2574-1030T>A
NM_001347922.1:c.968T>A	NP_001334851.1:p.Leu323His
NM_001347923.1:c.914T>A	NP_001334852.1:p.Leu305His
NM_001347924.1:c.659T>A	NP_001334853.1:p.Leu220His
NM_001347925.1:c.605T>A	NP_001334854.1:p.Leu202His
NM_001347926.1:c.714-1030T>A	NP_001334855.1:n.714-1030T>A
NM_001347927.1:c.359T>A	NP_001334856.1:p.Leu120His
NR_144939.1:n.3272T>A
XM_011542820.2:c.2873T>A	XP_011541122.1:p.Leu958His
XM_011542821.3:c.2765T>A	XP_011541123.1:p.Leu922His
XM_011542824.2:c.2003T>A	XP_011541126.1:p.Leu668His
XM_011542825.2:c.1160T>A	XP_011541127.1:p.Leu387His
XM_011542826.2:c.1025T>A	XP_011541128.1:p.Leu342His
XM_024448521.1:c.2885T>A	XP_024304289.1:p.Leu962His
XR_001747870.1:n.3710T>A
XR_001747872.1:n.3056T>A
XR_001747873.1:n.3370T>A
NM_001301089.2:c.779T>A	NP_001288018.1:p.Leu260His
NM_001347918.2:c.2519T>A	NP_001334847.2:p.Leu840His
NM_001347919.2:c.2574-1030T>A	NP_001334848.2:n.2574-1030T>A
NM_001347920.2:c.*21035T>A	NP_001334849.2:n.*21035T>A
NM_001347922.2:c.968T>A	NP_001334851.2:p.Leu323His
NM_001347923.2:c.914T>A	NP_001334852.2:p.Leu305His
NM_001347924.2:c.659T>A	NP_001334853.1:p.Leu220His
NM_001347925.2:c.605T>A	NP_001334854.1:p.Leu202His
NM_001347926.2:c.714-1030T>A	NP_001334855.1:n.714-1030T>A
NM_001347927.2:c.359T>A	NP_001334856.1:p.Leu120His
NM_014758.3:c.2639T>A MANE Select	NP_055573.3:p.Leu880His
NR_144939.2:n.3264T>A