Canonical Allele Identifier: CA383457838

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750643G>T (hg19) ; chr11:g.130880748G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880748G>T , CM000673.2:g.130880748G>T	GRCh38
NC_000011.9:g.130750643G>T , CM000673.1:g.130750643G>T	GRCh37
NC_000011.8:g.130255853G>T	NCBI36
NG_053190.1:g.40741C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265909.9:c.2632C>A MANE Select	ENSP00000265909.4:p.Leu878Met
ENST00000265909.8:c.2632C>A	ENSP00000265909.4:p.Leu878Met
ENST00000426933.6:c.136C>A	ENSP00000413345.2:p.Leu46Met
ENST00000526579.5:n.178-1037C>A
ENST00000527116.5:n.394C>A
ENST00000528555.5:c.772C>A	ENSP00000435122.1:p.Leu258Met
ENST00000530330.1:n.368C>A
ENST00000530356.5:c.772C>A	ENSP00000432307.1:p.Leu258Met
ENST00000533318.5:n.992C>A
ENST00000534726.5:c.352C>A	ENSP00000433699.1:p.Leu118Met
NM_001301089.1:c.772C>A	NP_001288018.1:p.Leu258Met
NM_014758.2:c.2632C>A	NP_055573.2:p.Leu878Met
XM_005271546.3:c.2574-1037C>A	XP_005271603.1:n.2574-1037C>A
XM_011542819.1:c.2878C>A	XP_011541121.1:p.Leu960Met
XM_011542820.1:c.2866C>A	XP_011541122.1:p.Leu956Met
XM_011542821.1:c.2758C>A	XP_011541123.1:p.Leu920Met
XM_011542824.1:c.1996C>A	XP_011541126.1:p.Leu666Met
XM_011542825.1:c.1153C>A	XP_011541127.1:p.Leu385Met
XM_011542826.1:c.1018C>A	XP_011541128.1:p.Leu340Met
XM_011542827.1:c.898C>A	XP_011541129.1:p.Leu300Met
NM_001347918.1:c.2512C>A	NP_001334847.1:p.Leu838Met
NM_001347919.1:c.2574-1037C>A	NP_001334848.1:n.2574-1037C>A
NM_001347922.1:c.961C>A	NP_001334851.1:p.Leu321Met
NM_001347923.1:c.907C>A	NP_001334852.1:p.Leu303Met
NM_001347924.1:c.652C>A	NP_001334853.1:p.Leu218Met
NM_001347925.1:c.598C>A	NP_001334854.1:p.Leu200Met
NM_001347926.1:c.714-1037C>A	NP_001334855.1:n.714-1037C>A
NM_001347927.1:c.352C>A	NP_001334856.1:p.Leu118Met
NR_144939.1:n.3265C>A
XM_011542820.2:c.2866C>A	XP_011541122.1:p.Leu956Met
XM_011542821.3:c.2758C>A	XP_011541123.1:p.Leu920Met
XM_011542824.2:c.1996C>A	XP_011541126.1:p.Leu666Met
XM_011542825.2:c.1153C>A	XP_011541127.1:p.Leu385Met
XM_011542826.2:c.1018C>A	XP_011541128.1:p.Leu340Met
XM_024448521.1:c.2878C>A	XP_024304289.1:p.Leu960Met
XR_001747870.1:n.3703C>A
XR_001747872.1:n.3049C>A
XR_001747873.1:n.3363C>A
NM_001301089.2:c.772C>A	NP_001288018.1:p.Leu258Met
NM_001347918.2:c.2512C>A	NP_001334847.2:p.Leu838Met
NM_001347919.2:c.2574-1037C>A	NP_001334848.2:n.2574-1037C>A
NM_001347920.2:c.*21028C>A	NP_001334849.2:n.*21028C>A
NM_001347922.2:c.961C>A	NP_001334851.2:p.Leu321Met
NM_001347923.2:c.907C>A	NP_001334852.2:p.Leu303Met
NM_001347924.2:c.652C>A	NP_001334853.1:p.Leu218Met
NM_001347925.2:c.598C>A	NP_001334854.1:p.Leu200Met
NM_001347926.2:c.714-1037C>A	NP_001334855.1:n.714-1037C>A
NM_001347927.2:c.352C>A	NP_001334856.1:p.Leu118Met
NM_014758.3:c.2632C>A MANE Select	NP_055573.3:p.Leu878Met
NR_144939.2:n.3257C>A