Canonical Allele Identifier: CA383457582

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750522A>C (hg19) ; chr11:g.130880627A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880627A>C , CM000673.2:g.130880627A>C	GRCh38
NC_000011.9:g.130750522A>C , CM000673.1:g.130750522A>C	GRCh37
NC_000011.8:g.130255732A>C	NCBI36
NG_053190.1:g.40862T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2753T>G MANE Select	ENSP00000265909.4:p.Leu918Arg
ENST00000265909.8:c.2753T>G	ENSP00000265909.4:p.Leu918Arg
ENST00000426933.6:c.257T>G	ENSP00000413345.2:p.Leu86Arg
ENST00000526579.5:n.178-916T>G
ENST00000527116.5:n.515T>G
ENST00000528555.5:c.893T>G	ENSP00000435122.1:p.Leu298Arg
ENST00000530330.1:n.489T>G
ENST00000530356.5:c.893T>G	ENSP00000432307.1:p.Leu298Arg
ENST00000533318.5:n.1113T>G
ENST00000534726.5:c.473T>G	ENSP00000433699.1:p.Leu158Arg
NM_001301089.1:c.893T>G	NP_001288018.1:p.Leu298Arg
NM_014758.2:c.2753T>G	NP_055573.2:p.Leu918Arg
XM_005271546.3:c.2574-916T>G	XP_005271603.1:n.2574-916T>G
XM_011542819.1:c.2999T>G	XP_011541121.1:p.Leu1000Arg
XM_011542820.1:c.2987T>G	XP_011541122.1:p.Leu996Arg
XM_011542821.1:c.2879T>G	XP_011541123.1:p.Leu960Arg
XM_011542824.1:c.2117T>G	XP_011541126.1:p.Leu706Arg
XM_011542825.1:c.1274T>G	XP_011541127.1:p.Leu425Arg
XM_011542826.1:c.1139T>G	XP_011541128.1:p.Leu380Arg
XM_011542827.1:c.1019T>G	XP_011541129.1:p.Leu340Arg
NM_001347918.1:c.2633T>G	NP_001334847.1:p.Leu878Arg
NM_001347919.1:c.2574-916T>G	NP_001334848.1:n.2574-916T>G
NM_001347922.1:c.1082T>G	NP_001334851.1:p.Leu361Arg
NM_001347923.1:c.1028T>G	NP_001334852.1:p.Leu343Arg
NM_001347924.1:c.773T>G	NP_001334853.1:p.Leu258Arg
NM_001347925.1:c.719T>G	NP_001334854.1:p.Leu240Arg
NM_001347926.1:c.714-916T>G	NP_001334855.1:n.714-916T>G
NM_001347927.1:c.473T>G	NP_001334856.1:p.Leu158Arg
NR_144939.1:n.3386T>G
XM_011542820.2:c.2987T>G	XP_011541122.1:p.Leu996Arg
XM_011542821.3:c.2879T>G	XP_011541123.1:p.Leu960Arg
XM_011542824.2:c.2117T>G	XP_011541126.1:p.Leu706Arg
XM_011542825.2:c.1274T>G	XP_011541127.1:p.Leu425Arg
XM_011542826.2:c.1139T>G	XP_011541128.1:p.Leu380Arg
XM_024448521.1:c.2999T>G	XP_024304289.1:p.Leu1000Arg
XR_001747870.1:n.3824T>G
XR_001747872.1:n.3170T>G
XR_001747873.1:n.3484T>G
NM_001301089.2:c.893T>G	NP_001288018.1:p.Leu298Arg
NM_001347918.2:c.2633T>G	NP_001334847.2:p.Leu878Arg
NM_001347919.2:c.2574-916T>G	NP_001334848.2:n.2574-916T>G
NM_001347920.2:c.*21149T>G	NP_001334849.2:n.*21149T>G
NM_001347922.2:c.1082T>G	NP_001334851.2:p.Leu361Arg
NM_001347923.2:c.1028T>G	NP_001334852.2:p.Leu343Arg
NM_001347924.2:c.773T>G	NP_001334853.1:p.Leu258Arg
NM_001347925.2:c.719T>G	NP_001334854.1:p.Leu240Arg
NM_001347926.2:c.714-916T>G	NP_001334855.1:n.714-916T>G
NM_001347927.2:c.473T>G	NP_001334856.1:p.Leu158Arg
NM_014758.3:c.2753T>G MANE Select	NP_055573.3:p.Leu918Arg
NR_144939.2:n.3378T>G