Canonical Allele Identifier: CA2009229614
Gene: SNX19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.130880633C= , CM000673.2:g.130880633C= GRCh38
NC_000011.9:g.130750528C= , CM000673.1:g.130750528C= GRCh37
NC_000011.8:g.130255738C= NCBI36
NG_053190.1:g.40856G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265909.9:c.2747G= MANE Select ENSP00000265909.4:p.Gly916=
ENST00000265909.8:c.2747G= ENSP00000265909.4:p.Gly916=
ENST00000426933.6:c.251G= ENSP00000413345.2:p.Gly84=
ENST00000526579.5:n.178-922G=
ENST00000527116.5:n.509G=
ENST00000528555.5:c.887G= ENSP00000435122.1:p.Gly296=
ENST00000530330.1:n.483G=
ENST00000530356.5:c.887G= ENSP00000432307.1:p.Gly296=
ENST00000533318.5:n.1107G=
ENST00000534726.5:c.467G= ENSP00000433699.1:p.Gly156=
NM_001301089.1:c.887G= NP_001288018.1:p.Gly296=
NM_014758.2:c.2747G= NP_055573.2:p.Gly916=
XM_005271546.3:c.2574-922G= XP_005271603.1:n.2574-922G=
XM_011542819.1:c.2993G= XP_011541121.1:p.Gly998=
XM_011542820.1:c.2981G= XP_011541122.1:p.Gly994=
XM_011542821.1:c.2873G= XP_011541123.1:p.Gly958=
XM_011542824.1:c.2111G= XP_011541126.1:p.Gly704=
XM_011542825.1:c.1268G= XP_011541127.1:p.Gly423=
XM_011542826.1:c.1133G= XP_011541128.1:p.Gly378=
XM_011542827.1:c.1013G= XP_011541129.1:p.Gly338=
NM_001347918.1:c.2627G= NP_001334847.1:p.Gly876=
NM_001347919.1:c.2574-922G= NP_001334848.1:n.2574-922G=
NM_001347922.1:c.1076G= NP_001334851.1:p.Gly359=
NM_001347923.1:c.1022G= NP_001334852.1:p.Gly341=
NM_001347924.1:c.767G= NP_001334853.1:p.Gly256=
NM_001347925.1:c.713G= NP_001334854.1:p.Gly238=
NM_001347926.1:c.714-922G= NP_001334855.1:n.714-922G=
NM_001347927.1:c.467G= NP_001334856.1:p.Gly156=
NR_144939.1:n.3380G=
XM_011542820.2:c.2981G= XP_011541122.1:p.Gly994=
XM_011542821.3:c.2873G= XP_011541123.1:p.Gly958=
XM_011542824.2:c.2111G= XP_011541126.1:p.Gly704=
XM_011542825.2:c.1268G= XP_011541127.1:p.Gly423=
XM_011542826.2:c.1133G= XP_011541128.1:p.Gly378=
XM_024448521.1:c.2993G= XP_024304289.1:p.Gly998=
XR_001747870.1:n.3818G=
XR_001747872.1:n.3164G=
XR_001747873.1:n.3478G=
NM_001301089.2:c.887G= NP_001288018.1:p.Gly296=
NM_001347918.2:c.2627G= NP_001334847.2:p.Gly876=
NM_001347919.2:c.2574-922G= NP_001334848.2:n.2574-922G=
NM_001347920.2:c.*21143G= NP_001334849.2:n.*21143G=
NM_001347922.2:c.1076G= NP_001334851.2:p.Gly359=
NM_001347923.2:c.1022G= NP_001334852.2:p.Gly341=
NM_001347924.2:c.767G= NP_001334853.1:p.Gly256=
NM_001347925.2:c.713G= NP_001334854.1:p.Gly238=
NM_001347926.2:c.714-922G= NP_001334855.1:n.714-922G=
NM_001347927.2:c.467G= NP_001334856.1:p.Gly156=
NM_014758.3:c.2747G= MANE Select NP_055573.3:p.Gly916=
NR_144939.2:n.3372G=