Canonical Allele Identifier: CA383457829

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750637G>A (hg19) ; chr11:g.130880742G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880742G>A , CM000673.2:g.130880742G>A	GRCh38
NC_000011.9:g.130750637G>A , CM000673.1:g.130750637G>A	GRCh37
NC_000011.8:g.130255847G>A	NCBI36
NG_053190.1:g.40747C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2638C>T MANE Select	ENSP00000265909.4:p.Leu880Phe
ENST00000265909.8:c.2638C>T	ENSP00000265909.4:p.Leu880Phe
ENST00000426933.6:c.142C>T	ENSP00000413345.2:p.Leu48Phe
ENST00000526579.5:n.178-1031C>T
ENST00000527116.5:n.400C>T
ENST00000528555.5:c.778C>T	ENSP00000435122.1:p.Leu260Phe
ENST00000530330.1:n.374C>T
ENST00000530356.5:c.778C>T	ENSP00000432307.1:p.Leu260Phe
ENST00000533318.5:n.998C>T
ENST00000534726.5:c.358C>T	ENSP00000433699.1:p.Leu120Phe
NM_001301089.1:c.778C>T	NP_001288018.1:p.Leu260Phe
NM_014758.2:c.2638C>T	NP_055573.2:p.Leu880Phe
XM_005271546.3:c.2574-1031C>T	XP_005271603.1:n.2574-1031C>T
XM_011542819.1:c.2884C>T	XP_011541121.1:p.Leu962Phe
XM_011542820.1:c.2872C>T	XP_011541122.1:p.Leu958Phe
XM_011542821.1:c.2764C>T	XP_011541123.1:p.Leu922Phe
XM_011542824.1:c.2002C>T	XP_011541126.1:p.Leu668Phe
XM_011542825.1:c.1159C>T	XP_011541127.1:p.Leu387Phe
XM_011542826.1:c.1024C>T	XP_011541128.1:p.Leu342Phe
XM_011542827.1:c.904C>T	XP_011541129.1:p.Leu302Phe
NM_001347918.1:c.2518C>T	NP_001334847.1:p.Leu840Phe
NM_001347919.1:c.2574-1031C>T	NP_001334848.1:n.2574-1031C>T
NM_001347922.1:c.967C>T	NP_001334851.1:p.Leu323Phe
NM_001347923.1:c.913C>T	NP_001334852.1:p.Leu305Phe
NM_001347924.1:c.658C>T	NP_001334853.1:p.Leu220Phe
NM_001347925.1:c.604C>T	NP_001334854.1:p.Leu202Phe
NM_001347926.1:c.714-1031C>T	NP_001334855.1:n.714-1031C>T
NM_001347927.1:c.358C>T	NP_001334856.1:p.Leu120Phe
NR_144939.1:n.3271C>T
XM_011542820.2:c.2872C>T	XP_011541122.1:p.Leu958Phe
XM_011542821.3:c.2764C>T	XP_011541123.1:p.Leu922Phe
XM_011542824.2:c.2002C>T	XP_011541126.1:p.Leu668Phe
XM_011542825.2:c.1159C>T	XP_011541127.1:p.Leu387Phe
XM_011542826.2:c.1024C>T	XP_011541128.1:p.Leu342Phe
XM_024448521.1:c.2884C>T	XP_024304289.1:p.Leu962Phe
XR_001747870.1:n.3709C>T
XR_001747872.1:n.3055C>T
XR_001747873.1:n.3369C>T
NM_001301089.2:c.778C>T	NP_001288018.1:p.Leu260Phe
NM_001347918.2:c.2518C>T	NP_001334847.2:p.Leu840Phe
NM_001347919.2:c.2574-1031C>T	NP_001334848.2:n.2574-1031C>T
NM_001347920.2:c.*21034C>T	NP_001334849.2:n.*21034C>T
NM_001347922.2:c.967C>T	NP_001334851.2:p.Leu323Phe
NM_001347923.2:c.913C>T	NP_001334852.2:p.Leu305Phe
NM_001347924.2:c.658C>T	NP_001334853.1:p.Leu220Phe
NM_001347925.2:c.604C>T	NP_001334854.1:p.Leu202Phe
NM_001347926.2:c.714-1031C>T	NP_001334855.1:n.714-1031C>T
NM_001347927.2:c.358C>T	NP_001334856.1:p.Leu120Phe
NM_014758.3:c.2638C>T MANE Select	NP_055573.3:p.Leu880Phe
NR_144939.2:n.3263C>T