Canonical Allele Identifier: CA2009229664
Gene: SNX19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.130880656T= , CM000673.2:g.130880656T= GRCh38
NC_000011.9:g.130750551T= , CM000673.1:g.130750551T= GRCh37
NC_000011.8:g.130255761T= NCBI36
NG_053190.1:g.40833A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265909.9:c.2724A= MANE Select ENSP00000265909.4:p.Lys908=
ENST00000265909.8:c.2724A= ENSP00000265909.4:p.Lys908=
ENST00000426933.6:c.228A= ENSP00000413345.2:p.Lys76=
ENST00000526579.5:n.178-945A=
ENST00000527116.5:n.486A=
ENST00000528555.5:c.864A= ENSP00000435122.1:p.Lys288=
ENST00000530330.1:n.460A=
ENST00000530356.5:c.864A= ENSP00000432307.1:p.Lys288=
ENST00000533318.5:n.1084A=
ENST00000534726.5:c.444A= ENSP00000433699.1:p.Lys148=
NM_001301089.1:c.864A= NP_001288018.1:p.Lys288=
NM_014758.2:c.2724A= NP_055573.2:p.Lys908=
XM_005271546.3:c.2574-945A= XP_005271603.1:n.2574-945A=
XM_011542819.1:c.2970A= XP_011541121.1:p.Lys990=
XM_011542820.1:c.2958A= XP_011541122.1:p.Lys986=
XM_011542821.1:c.2850A= XP_011541123.1:p.Lys950=
XM_011542824.1:c.2088A= XP_011541126.1:p.Lys696=
XM_011542825.1:c.1245A= XP_011541127.1:p.Lys415=
XM_011542826.1:c.1110A= XP_011541128.1:p.Lys370=
XM_011542827.1:c.990A= XP_011541129.1:p.Lys330=
NM_001347918.1:c.2604A= NP_001334847.1:p.Lys868=
NM_001347919.1:c.2574-945A= NP_001334848.1:n.2574-945A=
NM_001347922.1:c.1053A= NP_001334851.1:p.Lys351=
NM_001347923.1:c.999A= NP_001334852.1:p.Lys333=
NM_001347924.1:c.744A= NP_001334853.1:p.Lys248=
NM_001347925.1:c.690A= NP_001334854.1:p.Lys230=
NM_001347926.1:c.714-945A= NP_001334855.1:n.714-945A=
NM_001347927.1:c.444A= NP_001334856.1:p.Lys148=
NR_144939.1:n.3357A=
XM_011542820.2:c.2958A= XP_011541122.1:p.Lys986=
XM_011542821.3:c.2850A= XP_011541123.1:p.Lys950=
XM_011542824.2:c.2088A= XP_011541126.1:p.Lys696=
XM_011542825.2:c.1245A= XP_011541127.1:p.Lys415=
XM_011542826.2:c.1110A= XP_011541128.1:p.Lys370=
XM_024448521.1:c.2970A= XP_024304289.1:p.Lys990=
XR_001747870.1:n.3795A=
XR_001747872.1:n.3141A=
XR_001747873.1:n.3455A=
NM_001301089.2:c.864A= NP_001288018.1:p.Lys288=
NM_001347918.2:c.2604A= NP_001334847.2:p.Lys868=
NM_001347919.2:c.2574-945A= NP_001334848.2:n.2574-945A=
NM_001347920.2:c.*21120A= NP_001334849.2:n.*21120A=
NM_001347922.2:c.1053A= NP_001334851.2:p.Lys351=
NM_001347923.2:c.999A= NP_001334852.2:p.Lys333=
NM_001347924.2:c.744A= NP_001334853.1:p.Lys248=
NM_001347925.2:c.690A= NP_001334854.1:p.Lys230=
NM_001347926.2:c.714-945A= NP_001334855.1:n.714-945A=
NM_001347927.2:c.444A= NP_001334856.1:p.Lys148=
NM_014758.3:c.2724A= MANE Select NP_055573.3:p.Lys908=
NR_144939.2:n.3349A=