Canonical Allele Identifier: CA2616844417

Gene: SNX19

Linked Data

• gnomAD v4: 11-130880847-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880847G>C , CM000673.2:g.130880847G>C	GRCh38
NC_000011.9:g.130750742G>C , CM000673.1:g.130750742G>C	GRCh37
NC_000011.8:g.130255952G>C	NCBI36
NG_053190.1:g.40642C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2574-41C>G MANE Select	ENSP00000265909.4:n.2574-41C>G
ENST00000265909.8:c.2574-41C>G	ENSP00000265909.4:n.2574-41C>G
ENST00000426933.6:c.78-41C>G	ENSP00000413345.2:n.78-41C>G
ENST00000526579.5:n.178-1136C>G
ENST00000527116.5:n.295C>G
ENST00000528555.5:c.714-41C>G	ENSP00000435122.1:n.714-41C>G
ENST00000530330.1:n.310-41C>G
ENST00000530356.5:c.714-41C>G	ENSP00000432307.1:n.714-41C>G
ENST00000533318.5:n.934-41C>G
ENST00000534726.5:c.294-41C>G	ENSP00000433699.1:n.294-41C>G
NM_001301089.1:c.714-41C>G	NP_001288018.1:n.714-41C>G
NM_014758.2:c.2574-41C>G	NP_055573.2:n.2574-41C>G
XM_005271546.3:c.2574-1136C>G	XP_005271603.1:n.2574-1136C>G
XM_011542819.1:c.2820-41C>G	XP_011541121.1:n.2820-41C>G
XM_011542820.1:c.2808-41C>G	XP_011541122.1:n.2808-41C>G
XM_011542821.1:c.2700-41C>G	XP_011541123.1:n.2700-41C>G
XM_011542824.1:c.1938-41C>G	XP_011541126.1:n.1938-41C>G
XM_011542825.1:c.1095-41C>G	XP_011541127.1:n.1095-41C>G
XM_011542826.1:c.960-41C>G	XP_011541128.1:n.960-41C>G
XM_011542827.1:c.840-41C>G	XP_011541129.1:n.840-41C>G
NM_001347918.1:c.2454-41C>G	NP_001334847.1:n.2454-41C>G
NM_001347919.1:c.2574-1136C>G	NP_001334848.1:n.2574-1136C>G
NM_001347922.1:c.903-41C>G	NP_001334851.1:n.903-41C>G
NM_001347923.1:c.849-41C>G	NP_001334852.1:n.849-41C>G
NM_001347924.1:c.594-41C>G	NP_001334853.1:n.594-41C>G
NM_001347925.1:c.540-41C>G	NP_001334854.1:n.540-41C>G
NM_001347926.1:c.714-1136C>G	NP_001334855.1:n.714-1136C>G
NM_001347927.1:c.294-41C>G	NP_001334856.1:n.294-41C>G
NR_144939.1:n.3207-41C>G
XM_011542820.2:c.2808-41C>G	XP_011541122.1:n.2808-41C>G
XM_011542821.3:c.2700-41C>G	XP_011541123.1:n.2700-41C>G
XM_011542824.2:c.1938-41C>G	XP_011541126.1:n.1938-41C>G
XM_011542825.2:c.1095-41C>G	XP_011541127.1:n.1095-41C>G
XM_011542826.2:c.960-41C>G	XP_011541128.1:n.960-41C>G
XM_024448521.1:c.2820-41C>G	XP_024304289.1:n.2820-41C>G
XR_001747870.1:n.3645-41C>G
XR_001747872.1:n.2991-41C>G
XR_001747873.1:n.3305-41C>G
NM_001301089.2:c.714-41C>G	NP_001288018.1:n.714-41C>G
NM_001347918.2:c.2454-41C>G	NP_001334847.2:n.2454-41C>G
NM_001347919.2:c.2574-1136C>G	NP_001334848.2:n.2574-1136C>G
NM_001347920.2:c.*20929C>G	NP_001334849.2:n.*20929C>G
NM_001347922.2:c.903-41C>G	NP_001334851.2:n.903-41C>G
NM_001347923.2:c.849-41C>G	NP_001334852.2:n.849-41C>G
NM_001347924.2:c.594-41C>G	NP_001334853.1:n.594-41C>G
NM_001347925.2:c.540-41C>G	NP_001334854.1:n.540-41C>G
NM_001347926.2:c.714-1136C>G	NP_001334855.1:n.714-1136C>G
NM_001347927.2:c.294-41C>G	NP_001334856.1:n.294-41C>G
NM_014758.3:c.2574-41C>G MANE Select	NP_055573.3:n.2574-41C>G
NR_144939.2:n.3199-41C>G