Canonical Allele Identifier: CA383457654
Gene: SNX19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.130880658T>G , CM000673.2:g.130880658T>G GRCh38
NC_000011.9:g.130750553T>G , CM000673.1:g.130750553T>G GRCh37
NC_000011.8:g.130255763T>G NCBI36
NG_053190.1:g.40831A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265909.9:c.2722A>C MANE Select ENSP00000265909.4:p.Lys908Gln
ENST00000265909.8:c.2722A>C ENSP00000265909.4:p.Lys908Gln
ENST00000426933.6:c.226A>C ENSP00000413345.2:p.Lys76Gln
ENST00000526579.5:n.178-947A>C
ENST00000527116.5:n.484A>C
ENST00000528555.5:c.862A>C ENSP00000435122.1:p.Lys288Gln
ENST00000530330.1:n.458A>C
ENST00000530356.5:c.862A>C ENSP00000432307.1:p.Lys288Gln
ENST00000533318.5:n.1082A>C
ENST00000534726.5:c.442A>C ENSP00000433699.1:p.Lys148Gln
NM_001301089.1:c.862A>C NP_001288018.1:p.Lys288Gln
NM_014758.2:c.2722A>C NP_055573.2:p.Lys908Gln
XM_005271546.3:c.2574-947A>C XP_005271603.1:n.2574-947A>C
XM_011542819.1:c.2968A>C XP_011541121.1:p.Lys990Gln
XM_011542820.1:c.2956A>C XP_011541122.1:p.Lys986Gln
XM_011542821.1:c.2848A>C XP_011541123.1:p.Lys950Gln
XM_011542824.1:c.2086A>C XP_011541126.1:p.Lys696Gln
XM_011542825.1:c.1243A>C XP_011541127.1:p.Lys415Gln
XM_011542826.1:c.1108A>C XP_011541128.1:p.Lys370Gln
XM_011542827.1:c.988A>C XP_011541129.1:p.Lys330Gln
NM_001347918.1:c.2602A>C NP_001334847.1:p.Lys868Gln
NM_001347919.1:c.2574-947A>C NP_001334848.1:n.2574-947A>C
NM_001347922.1:c.1051A>C NP_001334851.1:p.Lys351Gln
NM_001347923.1:c.997A>C NP_001334852.1:p.Lys333Gln
NM_001347924.1:c.742A>C NP_001334853.1:p.Lys248Gln
NM_001347925.1:c.688A>C NP_001334854.1:p.Lys230Gln
NM_001347926.1:c.714-947A>C NP_001334855.1:n.714-947A>C
NM_001347927.1:c.442A>C NP_001334856.1:p.Lys148Gln
NR_144939.1:n.3355A>C
XM_011542820.2:c.2956A>C XP_011541122.1:p.Lys986Gln
XM_011542821.3:c.2848A>C XP_011541123.1:p.Lys950Gln
XM_011542824.2:c.2086A>C XP_011541126.1:p.Lys696Gln
XM_011542825.2:c.1243A>C XP_011541127.1:p.Lys415Gln
XM_011542826.2:c.1108A>C XP_011541128.1:p.Lys370Gln
XM_024448521.1:c.2968A>C XP_024304289.1:p.Lys990Gln
XR_001747870.1:n.3793A>C
XR_001747872.1:n.3139A>C
XR_001747873.1:n.3453A>C
NM_001301089.2:c.862A>C NP_001288018.1:p.Lys288Gln
NM_001347918.2:c.2602A>C NP_001334847.2:p.Lys868Gln
NM_001347919.2:c.2574-947A>C NP_001334848.2:n.2574-947A>C
NM_001347920.2:c.*21118A>C NP_001334849.2:n.*21118A>C
NM_001347922.2:c.1051A>C NP_001334851.2:p.Lys351Gln
NM_001347923.2:c.997A>C NP_001334852.2:p.Lys333Gln
NM_001347924.2:c.742A>C NP_001334853.1:p.Lys248Gln
NM_001347925.2:c.688A>C NP_001334854.1:p.Lys230Gln
NM_001347926.2:c.714-947A>C NP_001334855.1:n.714-947A>C
NM_001347927.2:c.442A>C NP_001334856.1:p.Lys148Gln
NM_014758.3:c.2722A>C MANE Select NP_055573.3:p.Lys908Gln
NR_144939.2:n.3347A>C