Canonical Allele Identifier: CA383457659
Gene: SNX19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.130880660T>C , CM000673.2:g.130880660T>C GRCh38
NC_000011.9:g.130750555T>C , CM000673.1:g.130750555T>C GRCh37
NC_000011.8:g.130255765T>C NCBI36
NG_053190.1:g.40829A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265909.9:c.2720A>G MANE Select ENSP00000265909.4:p.Glu907Gly
ENST00000265909.8:c.2720A>G ENSP00000265909.4:p.Glu907Gly
ENST00000426933.6:c.224A>G ENSP00000413345.2:p.Glu75Gly
ENST00000526579.5:n.178-949A>G
ENST00000527116.5:n.482A>G
ENST00000528555.5:c.860A>G ENSP00000435122.1:p.Glu287Gly
ENST00000530330.1:n.456A>G
ENST00000530356.5:c.860A>G ENSP00000432307.1:p.Glu287Gly
ENST00000533318.5:n.1080A>G
ENST00000534726.5:c.440A>G ENSP00000433699.1:p.Glu147Gly
NM_001301089.1:c.860A>G NP_001288018.1:p.Glu287Gly
NM_014758.2:c.2720A>G NP_055573.2:p.Glu907Gly
XM_005271546.3:c.2574-949A>G XP_005271603.1:n.2574-949A>G
XM_011542819.1:c.2966A>G XP_011541121.1:p.Glu989Gly
XM_011542820.1:c.2954A>G XP_011541122.1:p.Glu985Gly
XM_011542821.1:c.2846A>G XP_011541123.1:p.Glu949Gly
XM_011542824.1:c.2084A>G XP_011541126.1:p.Glu695Gly
XM_011542825.1:c.1241A>G XP_011541127.1:p.Glu414Gly
XM_011542826.1:c.1106A>G XP_011541128.1:p.Glu369Gly
XM_011542827.1:c.986A>G XP_011541129.1:p.Glu329Gly
NM_001347918.1:c.2600A>G NP_001334847.1:p.Glu867Gly
NM_001347919.1:c.2574-949A>G NP_001334848.1:n.2574-949A>G
NM_001347922.1:c.1049A>G NP_001334851.1:p.Glu350Gly
NM_001347923.1:c.995A>G NP_001334852.1:p.Glu332Gly
NM_001347924.1:c.740A>G NP_001334853.1:p.Glu247Gly
NM_001347925.1:c.686A>G NP_001334854.1:p.Glu229Gly
NM_001347926.1:c.714-949A>G NP_001334855.1:n.714-949A>G
NM_001347927.1:c.440A>G NP_001334856.1:p.Glu147Gly
NR_144939.1:n.3353A>G
XM_011542820.2:c.2954A>G XP_011541122.1:p.Glu985Gly
XM_011542821.3:c.2846A>G XP_011541123.1:p.Glu949Gly
XM_011542824.2:c.2084A>G XP_011541126.1:p.Glu695Gly
XM_011542825.2:c.1241A>G XP_011541127.1:p.Glu414Gly
XM_011542826.2:c.1106A>G XP_011541128.1:p.Glu369Gly
XM_024448521.1:c.2966A>G XP_024304289.1:p.Glu989Gly
XR_001747870.1:n.3791A>G
XR_001747872.1:n.3137A>G
XR_001747873.1:n.3451A>G
NM_001301089.2:c.860A>G NP_001288018.1:p.Glu287Gly
NM_001347918.2:c.2600A>G NP_001334847.2:p.Glu867Gly
NM_001347919.2:c.2574-949A>G NP_001334848.2:n.2574-949A>G
NM_001347920.2:c.*21116A>G NP_001334849.2:n.*21116A>G
NM_001347922.2:c.1049A>G NP_001334851.2:p.Glu350Gly
NM_001347923.2:c.995A>G NP_001334852.2:p.Glu332Gly
NM_001347924.2:c.740A>G NP_001334853.1:p.Glu247Gly
NM_001347925.2:c.686A>G NP_001334854.1:p.Glu229Gly
NM_001347926.2:c.714-949A>G NP_001334855.1:n.714-949A>G
NM_001347927.2:c.440A>G NP_001334856.1:p.Glu147Gly
NM_014758.3:c.2720A>G MANE Select NP_055573.3:p.Glu907Gly
NR_144939.2:n.3345A>G