Canonical Allele Identifier: CA383457874
Gene: SNX19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.130880766G>C , CM000673.2:g.130880766G>C GRCh38
NC_000011.9:g.130750661G>C , CM000673.1:g.130750661G>C GRCh37
NC_000011.8:g.130255871G>C NCBI36
NG_053190.1:g.40723C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265909.9:c.2614C>G MANE Select ENSP00000265909.4:p.Arg872Gly
ENST00000265909.8:c.2614C>G ENSP00000265909.4:p.Arg872Gly
ENST00000426933.6:c.118C>G ENSP00000413345.2:p.Arg40Gly
ENST00000526579.5:n.178-1055C>G
ENST00000527116.5:n.376C>G
ENST00000528555.5:c.754C>G ENSP00000435122.1:p.Arg252Gly
ENST00000530330.1:n.350C>G
ENST00000530356.5:c.754C>G ENSP00000432307.1:p.Arg252Gly
ENST00000533318.5:n.974C>G
ENST00000534726.5:c.334C>G ENSP00000433699.1:p.Arg112Gly
NM_001301089.1:c.754C>G NP_001288018.1:p.Arg252Gly
NM_014758.2:c.2614C>G NP_055573.2:p.Arg872Gly
XM_005271546.3:c.2574-1055C>G XP_005271603.1:n.2574-1055C>G
XM_011542819.1:c.2860C>G XP_011541121.1:p.Arg954Gly
XM_011542820.1:c.2848C>G XP_011541122.1:p.Arg950Gly
XM_011542821.1:c.2740C>G XP_011541123.1:p.Arg914Gly
XM_011542824.1:c.1978C>G XP_011541126.1:p.Arg660Gly
XM_011542825.1:c.1135C>G XP_011541127.1:p.Arg379Gly
XM_011542826.1:c.1000C>G XP_011541128.1:p.Arg334Gly
XM_011542827.1:c.880C>G XP_011541129.1:p.Arg294Gly
NM_001347918.1:c.2494C>G NP_001334847.1:p.Arg832Gly
NM_001347919.1:c.2574-1055C>G NP_001334848.1:n.2574-1055C>G
NM_001347922.1:c.943C>G NP_001334851.1:p.Arg315Gly
NM_001347923.1:c.889C>G NP_001334852.1:p.Arg297Gly
NM_001347924.1:c.634C>G NP_001334853.1:p.Arg212Gly
NM_001347925.1:c.580C>G NP_001334854.1:p.Arg194Gly
NM_001347926.1:c.714-1055C>G NP_001334855.1:n.714-1055C>G
NM_001347927.1:c.334C>G NP_001334856.1:p.Arg112Gly
NR_144939.1:n.3247C>G
XM_011542820.2:c.2848C>G XP_011541122.1:p.Arg950Gly
XM_011542821.3:c.2740C>G XP_011541123.1:p.Arg914Gly
XM_011542824.2:c.1978C>G XP_011541126.1:p.Arg660Gly
XM_011542825.2:c.1135C>G XP_011541127.1:p.Arg379Gly
XM_011542826.2:c.1000C>G XP_011541128.1:p.Arg334Gly
XM_024448521.1:c.2860C>G XP_024304289.1:p.Arg954Gly
XR_001747870.1:n.3685C>G
XR_001747872.1:n.3031C>G
XR_001747873.1:n.3345C>G
NM_001301089.2:c.754C>G NP_001288018.1:p.Arg252Gly
NM_001347918.2:c.2494C>G NP_001334847.2:p.Arg832Gly
NM_001347919.2:c.2574-1055C>G NP_001334848.2:n.2574-1055C>G
NM_001347920.2:c.*21010C>G NP_001334849.2:n.*21010C>G
NM_001347922.2:c.943C>G NP_001334851.2:p.Arg315Gly
NM_001347923.2:c.889C>G NP_001334852.2:p.Arg297Gly
NM_001347924.2:c.634C>G NP_001334853.1:p.Arg212Gly
NM_001347925.2:c.580C>G NP_001334854.1:p.Arg194Gly
NM_001347926.2:c.714-1055C>G NP_001334855.1:n.714-1055C>G
NM_001347927.2:c.334C>G NP_001334856.1:p.Arg112Gly
NM_014758.3:c.2614C>G MANE Select NP_055573.3:p.Arg872Gly
NR_144939.2:n.3239C>G