Canonical Allele Identifier: CA2009229938
Gene: SNX19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.130880770T= , CM000673.2:g.130880770T= GRCh38
NC_000011.9:g.130750665T= , CM000673.1:g.130750665T= GRCh37
NC_000011.8:g.130255875T= NCBI36
NG_053190.1:g.40719A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265909.9:c.2610A= MANE Select ENSP00000265909.4:p.Pro870=
ENST00000265909.8:c.2610A= ENSP00000265909.4:p.Pro870=
ENST00000426933.6:c.114A= ENSP00000413345.2:p.Pro38=
ENST00000526579.5:n.178-1059A=
ENST00000527116.5:n.372A=
ENST00000528555.5:c.750A= ENSP00000435122.1:p.Pro250=
ENST00000530330.1:n.346A=
ENST00000530356.5:c.750A= ENSP00000432307.1:p.Pro250=
ENST00000533318.5:n.970A=
ENST00000534726.5:c.330A= ENSP00000433699.1:p.Pro110=
NM_001301089.1:c.750A= NP_001288018.1:p.Pro250=
NM_014758.2:c.2610A= NP_055573.2:p.Pro870=
XM_005271546.3:c.2574-1059A= XP_005271603.1:n.2574-1059A=
XM_011542819.1:c.2856A= XP_011541121.1:p.Pro952=
XM_011542820.1:c.2844A= XP_011541122.1:p.Pro948=
XM_011542821.1:c.2736A= XP_011541123.1:p.Pro912=
XM_011542824.1:c.1974A= XP_011541126.1:p.Pro658=
XM_011542825.1:c.1131A= XP_011541127.1:p.Pro377=
XM_011542826.1:c.996A= XP_011541128.1:p.Pro332=
XM_011542827.1:c.876A= XP_011541129.1:p.Pro292=
NM_001347918.1:c.2490A= NP_001334847.1:p.Pro830=
NM_001347919.1:c.2574-1059A= NP_001334848.1:n.2574-1059A=
NM_001347922.1:c.939A= NP_001334851.1:p.Pro313=
NM_001347923.1:c.885A= NP_001334852.1:p.Pro295=
NM_001347924.1:c.630A= NP_001334853.1:p.Pro210=
NM_001347925.1:c.576A= NP_001334854.1:p.Pro192=
NM_001347926.1:c.714-1059A= NP_001334855.1:n.714-1059A=
NM_001347927.1:c.330A= NP_001334856.1:p.Pro110=
NR_144939.1:n.3243A=
XM_011542820.2:c.2844A= XP_011541122.1:p.Pro948=
XM_011542821.3:c.2736A= XP_011541123.1:p.Pro912=
XM_011542824.2:c.1974A= XP_011541126.1:p.Pro658=
XM_011542825.2:c.1131A= XP_011541127.1:p.Pro377=
XM_011542826.2:c.996A= XP_011541128.1:p.Pro332=
XM_024448521.1:c.2856A= XP_024304289.1:p.Pro952=
XR_001747870.1:n.3681A=
XR_001747872.1:n.3027A=
XR_001747873.1:n.3341A=
NM_001301089.2:c.750A= NP_001288018.1:p.Pro250=
NM_001347918.2:c.2490A= NP_001334847.2:p.Pro830=
NM_001347919.2:c.2574-1059A= NP_001334848.2:n.2574-1059A=
NM_001347920.2:c.*21006A= NP_001334849.2:n.*21006A=
NM_001347922.2:c.939A= NP_001334851.2:p.Pro313=
NM_001347923.2:c.885A= NP_001334852.2:p.Pro295=
NM_001347924.2:c.630A= NP_001334853.1:p.Pro210=
NM_001347925.2:c.576A= NP_001334854.1:p.Pro192=
NM_001347926.2:c.714-1059A= NP_001334855.1:n.714-1059A=
NM_001347927.2:c.330A= NP_001334856.1:p.Pro110=
NM_014758.3:c.2610A= MANE Select NP_055573.3:p.Pro870=
NR_144939.2:n.3235A=