Canonical Allele Identifier: CA383457678

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750565G>T (hg19) ; chr11:g.130880670G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880670G>T , CM000673.2:g.130880670G>T	GRCh38
NC_000011.9:g.130750565G>T , CM000673.1:g.130750565G>T	GRCh37
NC_000011.8:g.130255775G>T	NCBI36
NG_053190.1:g.40819C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2710C>A MANE Select	ENSP00000265909.4:p.Leu904Met
ENST00000265909.8:c.2710C>A	ENSP00000265909.4:p.Leu904Met
ENST00000426933.6:c.214C>A	ENSP00000413345.2:p.Leu72Met
ENST00000526579.5:n.178-959C>A
ENST00000527116.5:n.472C>A
ENST00000528555.5:c.850C>A	ENSP00000435122.1:p.Leu284Met
ENST00000530330.1:n.446C>A
ENST00000530356.5:c.850C>A	ENSP00000432307.1:p.Leu284Met
ENST00000533318.5:n.1070C>A
ENST00000534726.5:c.430C>A	ENSP00000433699.1:p.Leu144Met
NM_001301089.1:c.850C>A	NP_001288018.1:p.Leu284Met
NM_014758.2:c.2710C>A	NP_055573.2:p.Leu904Met
XM_005271546.3:c.2574-959C>A	XP_005271603.1:n.2574-959C>A
XM_011542819.1:c.2956C>A	XP_011541121.1:p.Leu986Met
XM_011542820.1:c.2944C>A	XP_011541122.1:p.Leu982Met
XM_011542821.1:c.2836C>A	XP_011541123.1:p.Leu946Met
XM_011542824.1:c.2074C>A	XP_011541126.1:p.Leu692Met
XM_011542825.1:c.1231C>A	XP_011541127.1:p.Leu411Met
XM_011542826.1:c.1096C>A	XP_011541128.1:p.Leu366Met
XM_011542827.1:c.976C>A	XP_011541129.1:p.Leu326Met
NM_001347918.1:c.2590C>A	NP_001334847.1:p.Leu864Met
NM_001347919.1:c.2574-959C>A	NP_001334848.1:n.2574-959C>A
NM_001347922.1:c.1039C>A	NP_001334851.1:p.Leu347Met
NM_001347923.1:c.985C>A	NP_001334852.1:p.Leu329Met
NM_001347924.1:c.730C>A	NP_001334853.1:p.Leu244Met
NM_001347925.1:c.676C>A	NP_001334854.1:p.Leu226Met
NM_001347926.1:c.714-959C>A	NP_001334855.1:n.714-959C>A
NM_001347927.1:c.430C>A	NP_001334856.1:p.Leu144Met
NR_144939.1:n.3343C>A
XM_011542820.2:c.2944C>A	XP_011541122.1:p.Leu982Met
XM_011542821.3:c.2836C>A	XP_011541123.1:p.Leu946Met
XM_011542824.2:c.2074C>A	XP_011541126.1:p.Leu692Met
XM_011542825.2:c.1231C>A	XP_011541127.1:p.Leu411Met
XM_011542826.2:c.1096C>A	XP_011541128.1:p.Leu366Met
XM_024448521.1:c.2956C>A	XP_024304289.1:p.Leu986Met
XR_001747870.1:n.3781C>A
XR_001747872.1:n.3127C>A
XR_001747873.1:n.3441C>A
NM_001301089.2:c.850C>A	NP_001288018.1:p.Leu284Met
NM_001347918.2:c.2590C>A	NP_001334847.2:p.Leu864Met
NM_001347919.2:c.2574-959C>A	NP_001334848.2:n.2574-959C>A
NM_001347920.2:c.*21106C>A	NP_001334849.2:n.*21106C>A
NM_001347922.2:c.1039C>A	NP_001334851.2:p.Leu347Met
NM_001347923.2:c.985C>A	NP_001334852.2:p.Leu329Met
NM_001347924.2:c.730C>A	NP_001334853.1:p.Leu244Met
NM_001347925.2:c.676C>A	NP_001334854.1:p.Leu226Met
NM_001347926.2:c.714-959C>A	NP_001334855.1:n.714-959C>A
NM_001347927.2:c.430C>A	NP_001334856.1:p.Leu144Met
NM_014758.3:c.2710C>A MANE Select	NP_055573.3:p.Leu904Met
NR_144939.2:n.3335C>A