Canonical Allele Identifier: CA2009229650
Gene: SNX19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.130880652C= , CM000673.2:g.130880652C= GRCh38
NC_000011.9:g.130750547C= , CM000673.1:g.130750547C= GRCh37
NC_000011.8:g.130255757C= NCBI36
NG_053190.1:g.40837G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265909.9:c.2728G= MANE Select ENSP00000265909.4:p.Ala910=
ENST00000265909.8:c.2728G= ENSP00000265909.4:p.Ala910=
ENST00000426933.6:c.232G= ENSP00000413345.2:p.Ala78=
ENST00000526579.5:n.178-941G=
ENST00000527116.5:n.490G=
ENST00000528555.5:c.868G= ENSP00000435122.1:p.Ala290=
ENST00000530330.1:n.464G=
ENST00000530356.5:c.868G= ENSP00000432307.1:p.Ala290=
ENST00000533318.5:n.1088G=
ENST00000534726.5:c.448G= ENSP00000433699.1:p.Ala150=
NM_001301089.1:c.868G= NP_001288018.1:p.Ala290=
NM_014758.2:c.2728G= NP_055573.2:p.Ala910=
XM_005271546.3:c.2574-941G= XP_005271603.1:n.2574-941G=
XM_011542819.1:c.2974G= XP_011541121.1:p.Ala992=
XM_011542820.1:c.2962G= XP_011541122.1:p.Ala988=
XM_011542821.1:c.2854G= XP_011541123.1:p.Ala952=
XM_011542824.1:c.2092G= XP_011541126.1:p.Ala698=
XM_011542825.1:c.1249G= XP_011541127.1:p.Ala417=
XM_011542826.1:c.1114G= XP_011541128.1:p.Ala372=
XM_011542827.1:c.994G= XP_011541129.1:p.Ala332=
NM_001347918.1:c.2608G= NP_001334847.1:p.Ala870=
NM_001347919.1:c.2574-941G= NP_001334848.1:n.2574-941G=
NM_001347922.1:c.1057G= NP_001334851.1:p.Ala353=
NM_001347923.1:c.1003G= NP_001334852.1:p.Ala335=
NM_001347924.1:c.748G= NP_001334853.1:p.Ala250=
NM_001347925.1:c.694G= NP_001334854.1:p.Ala232=
NM_001347926.1:c.714-941G= NP_001334855.1:n.714-941G=
NM_001347927.1:c.448G= NP_001334856.1:p.Ala150=
NR_144939.1:n.3361G=
XM_011542820.2:c.2962G= XP_011541122.1:p.Ala988=
XM_011542821.3:c.2854G= XP_011541123.1:p.Ala952=
XM_011542824.2:c.2092G= XP_011541126.1:p.Ala698=
XM_011542825.2:c.1249G= XP_011541127.1:p.Ala417=
XM_011542826.2:c.1114G= XP_011541128.1:p.Ala372=
XM_024448521.1:c.2974G= XP_024304289.1:p.Ala992=
XR_001747870.1:n.3799G=
XR_001747872.1:n.3145G=
XR_001747873.1:n.3459G=
NM_001301089.2:c.868G= NP_001288018.1:p.Ala290=
NM_001347918.2:c.2608G= NP_001334847.2:p.Ala870=
NM_001347919.2:c.2574-941G= NP_001334848.2:n.2574-941G=
NM_001347920.2:c.*21124G= NP_001334849.2:n.*21124G=
NM_001347922.2:c.1057G= NP_001334851.2:p.Ala353=
NM_001347923.2:c.1003G= NP_001334852.2:p.Ala335=
NM_001347924.2:c.748G= NP_001334853.1:p.Ala250=
NM_001347925.2:c.694G= NP_001334854.1:p.Ala232=
NM_001347926.2:c.714-941G= NP_001334855.1:n.714-941G=
NM_001347927.2:c.448G= NP_001334856.1:p.Ala150=
NM_014758.3:c.2728G= MANE Select NP_055573.3:p.Ala910=
NR_144939.2:n.3353G=