Canonical Allele Identifier: CA383457699
Gene: SNX19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.130880679C>T , CM000673.2:g.130880679C>T GRCh38
NC_000011.9:g.130750574C>T , CM000673.1:g.130750574C>T GRCh37
NC_000011.8:g.130255784C>T NCBI36
NG_053190.1:g.40810G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265909.9:c.2701G>A MANE Select ENSP00000265909.4:p.Glu901Lys
ENST00000265909.8:c.2701G>A ENSP00000265909.4:p.Glu901Lys
ENST00000426933.6:c.205G>A ENSP00000413345.2:p.Glu69Lys
ENST00000526579.5:n.178-968G>A
ENST00000527116.5:n.463G>A
ENST00000528555.5:c.841G>A ENSP00000435122.1:p.Glu281Lys
ENST00000530330.1:n.437G>A
ENST00000530356.5:c.841G>A ENSP00000432307.1:p.Glu281Lys
ENST00000533318.5:n.1061G>A
ENST00000534726.5:c.421G>A ENSP00000433699.1:p.Glu141Lys
NM_001301089.1:c.841G>A NP_001288018.1:p.Glu281Lys
NM_014758.2:c.2701G>A NP_055573.2:p.Glu901Lys
XM_005271546.3:c.2574-968G>A XP_005271603.1:n.2574-968G>A
XM_011542819.1:c.2947G>A XP_011541121.1:p.Glu983Lys
XM_011542820.1:c.2935G>A XP_011541122.1:p.Glu979Lys
XM_011542821.1:c.2827G>A XP_011541123.1:p.Glu943Lys
XM_011542824.1:c.2065G>A XP_011541126.1:p.Glu689Lys
XM_011542825.1:c.1222G>A XP_011541127.1:p.Glu408Lys
XM_011542826.1:c.1087G>A XP_011541128.1:p.Glu363Lys
XM_011542827.1:c.967G>A XP_011541129.1:p.Glu323Lys
NM_001347918.1:c.2581G>A NP_001334847.1:p.Glu861Lys
NM_001347919.1:c.2574-968G>A NP_001334848.1:n.2574-968G>A
NM_001347922.1:c.1030G>A NP_001334851.1:p.Glu344Lys
NM_001347923.1:c.976G>A NP_001334852.1:p.Glu326Lys
NM_001347924.1:c.721G>A NP_001334853.1:p.Glu241Lys
NM_001347925.1:c.667G>A NP_001334854.1:p.Glu223Lys
NM_001347926.1:c.714-968G>A NP_001334855.1:n.714-968G>A
NM_001347927.1:c.421G>A NP_001334856.1:p.Glu141Lys
NR_144939.1:n.3334G>A
XM_011542820.2:c.2935G>A XP_011541122.1:p.Glu979Lys
XM_011542821.3:c.2827G>A XP_011541123.1:p.Glu943Lys
XM_011542824.2:c.2065G>A XP_011541126.1:p.Glu689Lys
XM_011542825.2:c.1222G>A XP_011541127.1:p.Glu408Lys
XM_011542826.2:c.1087G>A XP_011541128.1:p.Glu363Lys
XM_024448521.1:c.2947G>A XP_024304289.1:p.Glu983Lys
XR_001747870.1:n.3772G>A
XR_001747872.1:n.3118G>A
XR_001747873.1:n.3432G>A
NM_001301089.2:c.841G>A NP_001288018.1:p.Glu281Lys
NM_001347918.2:c.2581G>A NP_001334847.2:p.Glu861Lys
NM_001347919.2:c.2574-968G>A NP_001334848.2:n.2574-968G>A
NM_001347920.2:c.*21097G>A NP_001334849.2:n.*21097G>A
NM_001347922.2:c.1030G>A NP_001334851.2:p.Glu344Lys
NM_001347923.2:c.976G>A NP_001334852.2:p.Glu326Lys
NM_001347924.2:c.721G>A NP_001334853.1:p.Glu241Lys
NM_001347925.2:c.667G>A NP_001334854.1:p.Glu223Lys
NM_001347926.2:c.714-968G>A NP_001334855.1:n.714-968G>A
NM_001347927.2:c.421G>A NP_001334856.1:p.Glu141Lys
NM_014758.3:c.2701G>A MANE Select NP_055573.3:p.Glu901Lys
NR_144939.2:n.3326G>A