Canonical Allele Identifier: CA2009229635
Gene: SNX19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.130880641G= , CM000673.2:g.130880641G= GRCh38
NC_000011.9:g.130750536G= , CM000673.1:g.130750536G= GRCh37
NC_000011.8:g.130255746G= NCBI36
NG_053190.1:g.40848C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265909.9:c.2739C= MANE Select ENSP00000265909.4:p.Ser913=
ENST00000265909.8:c.2739C= ENSP00000265909.4:p.Ser913=
ENST00000426933.6:c.243C= ENSP00000413345.2:p.Ser81=
ENST00000526579.5:n.178-930C=
ENST00000527116.5:n.501C=
ENST00000528555.5:c.879C= ENSP00000435122.1:p.Ser293=
ENST00000530330.1:n.475C=
ENST00000530356.5:c.879C= ENSP00000432307.1:p.Ser293=
ENST00000533318.5:n.1099C=
ENST00000534726.5:c.459C= ENSP00000433699.1:p.Ser153=
NM_001301089.1:c.879C= NP_001288018.1:p.Ser293=
NM_014758.2:c.2739C= NP_055573.2:p.Ser913=
XM_005271546.3:c.2574-930C= XP_005271603.1:n.2574-930C=
XM_011542819.1:c.2985C= XP_011541121.1:p.Ser995=
XM_011542820.1:c.2973C= XP_011541122.1:p.Ser991=
XM_011542821.1:c.2865C= XP_011541123.1:p.Ser955=
XM_011542824.1:c.2103C= XP_011541126.1:p.Ser701=
XM_011542825.1:c.1260C= XP_011541127.1:p.Ser420=
XM_011542826.1:c.1125C= XP_011541128.1:p.Ser375=
XM_011542827.1:c.1005C= XP_011541129.1:p.Ser335=
NM_001347918.1:c.2619C= NP_001334847.1:p.Ser873=
NM_001347919.1:c.2574-930C= NP_001334848.1:n.2574-930C=
NM_001347922.1:c.1068C= NP_001334851.1:p.Ser356=
NM_001347923.1:c.1014C= NP_001334852.1:p.Ser338=
NM_001347924.1:c.759C= NP_001334853.1:p.Ser253=
NM_001347925.1:c.705C= NP_001334854.1:p.Ser235=
NM_001347926.1:c.714-930C= NP_001334855.1:n.714-930C=
NM_001347927.1:c.459C= NP_001334856.1:p.Ser153=
NR_144939.1:n.3372C=
XM_011542820.2:c.2973C= XP_011541122.1:p.Ser991=
XM_011542821.3:c.2865C= XP_011541123.1:p.Ser955=
XM_011542824.2:c.2103C= XP_011541126.1:p.Ser701=
XM_011542825.2:c.1260C= XP_011541127.1:p.Ser420=
XM_011542826.2:c.1125C= XP_011541128.1:p.Ser375=
XM_024448521.1:c.2985C= XP_024304289.1:p.Ser995=
XR_001747870.1:n.3810C=
XR_001747872.1:n.3156C=
XR_001747873.1:n.3470C=
NM_001301089.2:c.879C= NP_001288018.1:p.Ser293=
NM_001347918.2:c.2619C= NP_001334847.2:p.Ser873=
NM_001347919.2:c.2574-930C= NP_001334848.2:n.2574-930C=
NM_001347920.2:c.*21135C= NP_001334849.2:n.*21135C=
NM_001347922.2:c.1068C= NP_001334851.2:p.Ser356=
NM_001347923.2:c.1014C= NP_001334852.2:p.Ser338=
NM_001347924.2:c.759C= NP_001334853.1:p.Ser253=
NM_001347925.2:c.705C= NP_001334854.1:p.Ser235=
NM_001347926.2:c.714-930C= NP_001334855.1:n.714-930C=
NM_001347927.2:c.459C= NP_001334856.1:p.Ser153=
NM_014758.3:c.2739C= MANE Select NP_055573.3:p.Ser913=
NR_144939.2:n.3364C=