Canonical Allele Identifier: CA383457642

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750549T>A (hg19) ; chr11:g.130880654T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880654T>A , CM000673.2:g.130880654T>A	GRCh38
NC_000011.9:g.130750549T>A , CM000673.1:g.130750549T>A	GRCh37
NC_000011.8:g.130255759T>A	NCBI36
NG_053190.1:g.40835A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2726A>T MANE Select	ENSP00000265909.4:p.Gln909Leu
ENST00000265909.8:c.2726A>T	ENSP00000265909.4:p.Gln909Leu
ENST00000426933.6:c.230A>T	ENSP00000413345.2:p.Gln77Leu
ENST00000526579.5:n.178-943A>T
ENST00000527116.5:n.488A>T
ENST00000528555.5:c.866A>T	ENSP00000435122.1:p.Gln289Leu
ENST00000530330.1:n.462A>T
ENST00000530356.5:c.866A>T	ENSP00000432307.1:p.Gln289Leu
ENST00000533318.5:n.1086A>T
ENST00000534726.5:c.446A>T	ENSP00000433699.1:p.Gln149Leu
NM_001301089.1:c.866A>T	NP_001288018.1:p.Gln289Leu
NM_014758.2:c.2726A>T	NP_055573.2:p.Gln909Leu
XM_005271546.3:c.2574-943A>T	XP_005271603.1:n.2574-943A>T
XM_011542819.1:c.2972A>T	XP_011541121.1:p.Gln991Leu
XM_011542820.1:c.2960A>T	XP_011541122.1:p.Gln987Leu
XM_011542821.1:c.2852A>T	XP_011541123.1:p.Gln951Leu
XM_011542824.1:c.2090A>T	XP_011541126.1:p.Gln697Leu
XM_011542825.1:c.1247A>T	XP_011541127.1:p.Gln416Leu
XM_011542826.1:c.1112A>T	XP_011541128.1:p.Gln371Leu
XM_011542827.1:c.992A>T	XP_011541129.1:p.Gln331Leu
NM_001347918.1:c.2606A>T	NP_001334847.1:p.Gln869Leu
NM_001347919.1:c.2574-943A>T	NP_001334848.1:n.2574-943A>T
NM_001347922.1:c.1055A>T	NP_001334851.1:p.Gln352Leu
NM_001347923.1:c.1001A>T	NP_001334852.1:p.Gln334Leu
NM_001347924.1:c.746A>T	NP_001334853.1:p.Gln249Leu
NM_001347925.1:c.692A>T	NP_001334854.1:p.Gln231Leu
NM_001347926.1:c.714-943A>T	NP_001334855.1:n.714-943A>T
NM_001347927.1:c.446A>T	NP_001334856.1:p.Gln149Leu
NR_144939.1:n.3359A>T
XM_011542820.2:c.2960A>T	XP_011541122.1:p.Gln987Leu
XM_011542821.3:c.2852A>T	XP_011541123.1:p.Gln951Leu
XM_011542824.2:c.2090A>T	XP_011541126.1:p.Gln697Leu
XM_011542825.2:c.1247A>T	XP_011541127.1:p.Gln416Leu
XM_011542826.2:c.1112A>T	XP_011541128.1:p.Gln371Leu
XM_024448521.1:c.2972A>T	XP_024304289.1:p.Gln991Leu
XR_001747870.1:n.3797A>T
XR_001747872.1:n.3143A>T
XR_001747873.1:n.3457A>T
NM_001301089.2:c.866A>T	NP_001288018.1:p.Gln289Leu
NM_001347918.2:c.2606A>T	NP_001334847.2:p.Gln869Leu
NM_001347919.2:c.2574-943A>T	NP_001334848.2:n.2574-943A>T
NM_001347920.2:c.*21122A>T	NP_001334849.2:n.*21122A>T
NM_001347922.2:c.1055A>T	NP_001334851.2:p.Gln352Leu
NM_001347923.2:c.1001A>T	NP_001334852.2:p.Gln334Leu
NM_001347924.2:c.746A>T	NP_001334853.1:p.Gln249Leu
NM_001347925.2:c.692A>T	NP_001334854.1:p.Gln231Leu
NM_001347926.2:c.714-943A>T	NP_001334855.1:n.714-943A>T
NM_001347927.2:c.446A>T	NP_001334856.1:p.Gln149Leu
NM_014758.3:c.2726A>T MANE Select	NP_055573.3:p.Gln909Leu
NR_144939.2:n.3351A>T