Canonical Allele Identifier: CA477582271

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750563C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880668C>T , CM000673.2:g.130880668C>T	GRCh38
NC_000011.9:g.130750563C>T , CM000673.1:g.130750563C>T	GRCh37
NC_000011.8:g.130255773C>T	NCBI36
NG_053190.1:g.40821G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2712G>A MANE Select	ENSP00000265909.4:p.Leu904=
ENST00000265909.8:c.2712G>A	ENSP00000265909.4:p.Leu904=
ENST00000426933.6:c.216G>A	ENSP00000413345.2:p.Leu72=
ENST00000526579.5:n.178-957G>A
ENST00000527116.5:n.474G>A
ENST00000528555.5:c.852G>A	ENSP00000435122.1:p.Leu284=
ENST00000530330.1:n.448G>A
ENST00000530356.5:c.852G>A	ENSP00000432307.1:p.Leu284=
ENST00000533318.5:n.1072G>A
ENST00000534726.5:c.432G>A	ENSP00000433699.1:p.Leu144=
NM_001301089.1:c.852G>A	NP_001288018.1:p.Leu284=
NM_014758.2:c.2712G>A	NP_055573.2:p.Leu904=
XM_005271546.3:c.2574-957G>A	XP_005271603.1:n.2574-957G>A
XM_011542819.1:c.2958G>A	XP_011541121.1:p.Leu986=
XM_011542820.1:c.2946G>A	XP_011541122.1:p.Leu982=
XM_011542821.1:c.2838G>A	XP_011541123.1:p.Leu946=
XM_011542824.1:c.2076G>A	XP_011541126.1:p.Leu692=
XM_011542825.1:c.1233G>A	XP_011541127.1:p.Leu411=
XM_011542826.1:c.1098G>A	XP_011541128.1:p.Leu366=
XM_011542827.1:c.978G>A	XP_011541129.1:p.Leu326=
NM_001347918.1:c.2592G>A	NP_001334847.1:p.Leu864=
NM_001347919.1:c.2574-957G>A	NP_001334848.1:n.2574-957G>A
NM_001347922.1:c.1041G>A	NP_001334851.1:p.Leu347=
NM_001347923.1:c.987G>A	NP_001334852.1:p.Leu329=
NM_001347924.1:c.732G>A	NP_001334853.1:p.Leu244=
NM_001347925.1:c.678G>A	NP_001334854.1:p.Leu226=
NM_001347926.1:c.714-957G>A	NP_001334855.1:n.714-957G>A
NM_001347927.1:c.432G>A	NP_001334856.1:p.Leu144=
NR_144939.1:n.3345G>A
XM_011542820.2:c.2946G>A	XP_011541122.1:p.Leu982=
XM_011542821.3:c.2838G>A	XP_011541123.1:p.Leu946=
XM_011542824.2:c.2076G>A	XP_011541126.1:p.Leu692=
XM_011542825.2:c.1233G>A	XP_011541127.1:p.Leu411=
XM_011542826.2:c.1098G>A	XP_011541128.1:p.Leu366=
XM_024448521.1:c.2958G>A	XP_024304289.1:p.Leu986=
XR_001747870.1:n.3783G>A
XR_001747872.1:n.3129G>A
XR_001747873.1:n.3443G>A
NM_001301089.2:c.852G>A	NP_001288018.1:p.Leu284=
NM_001347918.2:c.2592G>A	NP_001334847.2:p.Leu864=
NM_001347919.2:c.2574-957G>A	NP_001334848.2:n.2574-957G>A
NM_001347920.2:c.*21108G>A	NP_001334849.2:n.*21108G>A
NM_001347922.2:c.1041G>A	NP_001334851.2:p.Leu347=
NM_001347923.2:c.987G>A	NP_001334852.2:p.Leu329=
NM_001347924.2:c.732G>A	NP_001334853.1:p.Leu244=
NM_001347925.2:c.678G>A	NP_001334854.1:p.Leu226=
NM_001347926.2:c.714-957G>A	NP_001334855.1:n.714-957G>A
NM_001347927.2:c.432G>A	NP_001334856.1:p.Leu144=
NM_014758.3:c.2712G>A MANE Select	NP_055573.3:p.Leu904=
NR_144939.2:n.3337G>A