Canonical Allele Identifier: CA6366586

Gene: SNX19

Linked Data

• dbSNP Id: rs766376350
• ExAC: 11:130750631 C / A
• gnomAD v2: 11-130750631-C-A
• gnomAD v3: 11-130880736-C-A
• gnomAD v4: 11-130880736-C-A
• MyVariant Identifiers: chr11:g.130750631C>A (hg19) ; chr11:g.130880736C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880736C>A , CM000673.2:g.130880736C>A	GRCh38
NC_000011.9:g.130750631C>A , CM000673.1:g.130750631C>A	GRCh37
NC_000011.8:g.130255841C>A	NCBI36
NG_053190.1:g.40753G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2644G>T MANE Select	ENSP00000265909.4:p.Glu882Ter
ENST00000265909.8:c.2644G>T	ENSP00000265909.4:p.Glu882Ter
ENST00000426933.6:c.148G>T	ENSP00000413345.2:p.Glu50Ter
ENST00000526579.5:n.178-1025G>T
ENST00000527116.5:n.406G>T
ENST00000528555.5:c.784G>T	ENSP00000435122.1:p.Glu262Ter
ENST00000530330.1:n.380G>T
ENST00000530356.5:c.784G>T	ENSP00000432307.1:p.Glu262Ter
ENST00000533318.5:n.1004G>T
ENST00000534726.5:c.364G>T	ENSP00000433699.1:p.Glu122Ter
NM_001301089.1:c.784G>T	NP_001288018.1:p.Glu262Ter
NM_014758.2:c.2644G>T	NP_055573.2:p.Glu882Ter
XM_005271546.3:c.2574-1025G>T	XP_005271603.1:n.2574-1025G>T
XM_011542819.1:c.2890G>T	XP_011541121.1:p.Glu964Ter
XM_011542820.1:c.2878G>T	XP_011541122.1:p.Glu960Ter
XM_011542821.1:c.2770G>T	XP_011541123.1:p.Glu924Ter
XM_011542824.1:c.2008G>T	XP_011541126.1:p.Glu670Ter
XM_011542825.1:c.1165G>T	XP_011541127.1:p.Glu389Ter
XM_011542826.1:c.1030G>T	XP_011541128.1:p.Glu344Ter
XM_011542827.1:c.910G>T	XP_011541129.1:p.Glu304Ter
NM_001347918.1:c.2524G>T	NP_001334847.1:p.Glu842Ter
NM_001347919.1:c.2574-1025G>T	NP_001334848.1:n.2574-1025G>T
NM_001347922.1:c.973G>T	NP_001334851.1:p.Glu325Ter
NM_001347923.1:c.919G>T	NP_001334852.1:p.Glu307Ter
NM_001347924.1:c.664G>T	NP_001334853.1:p.Glu222Ter
NM_001347925.1:c.610G>T	NP_001334854.1:p.Glu204Ter
NM_001347926.1:c.714-1025G>T	NP_001334855.1:n.714-1025G>T
NM_001347927.1:c.364G>T	NP_001334856.1:p.Glu122Ter
NR_144939.1:n.3277G>T
XM_011542820.2:c.2878G>T	XP_011541122.1:p.Glu960Ter
XM_011542821.3:c.2770G>T	XP_011541123.1:p.Glu924Ter
XM_011542824.2:c.2008G>T	XP_011541126.1:p.Glu670Ter
XM_011542825.2:c.1165G>T	XP_011541127.1:p.Glu389Ter
XM_011542826.2:c.1030G>T	XP_011541128.1:p.Glu344Ter
XM_024448521.1:c.2890G>T	XP_024304289.1:p.Glu964Ter
XR_001747870.1:n.3715G>T
XR_001747872.1:n.3061G>T
XR_001747873.1:n.3375G>T
NM_001301089.2:c.784G>T	NP_001288018.1:p.Glu262Ter
NM_001347918.2:c.2524G>T	NP_001334847.2:p.Glu842Ter
NM_001347919.2:c.2574-1025G>T	NP_001334848.2:n.2574-1025G>T
NM_001347920.2:c.*21040G>T	NP_001334849.2:n.*21040G>T
NM_001347922.2:c.973G>T	NP_001334851.2:p.Glu325Ter
NM_001347923.2:c.919G>T	NP_001334852.2:p.Glu307Ter
NM_001347924.2:c.664G>T	NP_001334853.1:p.Glu222Ter
NM_001347925.2:c.610G>T	NP_001334854.1:p.Glu204Ter
NM_001347926.2:c.714-1025G>T	NP_001334855.1:n.714-1025G>T
NM_001347927.2:c.364G>T	NP_001334856.1:p.Glu122Ter
NM_014758.3:c.2644G>T MANE Select	NP_055573.3:p.Glu882Ter
NR_144939.2:n.3269G>T