Canonical Allele Identifier: CA383457808

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750628A>C (hg19) ; chr11:g.130880733A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880733A>C , CM000673.2:g.130880733A>C	GRCh38
NC_000011.9:g.130750628A>C , CM000673.1:g.130750628A>C	GRCh37
NC_000011.8:g.130255838A>C	NCBI36
NG_053190.1:g.40756T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2647T>G MANE Select	ENSP00000265909.4:p.Ser883Ala
ENST00000265909.8:c.2647T>G	ENSP00000265909.4:p.Ser883Ala
ENST00000426933.6:c.151T>G	ENSP00000413345.2:p.Ser51Ala
ENST00000526579.5:n.178-1022T>G
ENST00000527116.5:n.409T>G
ENST00000528555.5:c.787T>G	ENSP00000435122.1:p.Ser263Ala
ENST00000530330.1:n.383T>G
ENST00000530356.5:c.787T>G	ENSP00000432307.1:p.Ser263Ala
ENST00000533318.5:n.1007T>G
ENST00000534726.5:c.367T>G	ENSP00000433699.1:p.Ser123Ala
NM_001301089.1:c.787T>G	NP_001288018.1:p.Ser263Ala
NM_014758.2:c.2647T>G	NP_055573.2:p.Ser883Ala
XM_005271546.3:c.2574-1022T>G	XP_005271603.1:n.2574-1022T>G
XM_011542819.1:c.2893T>G	XP_011541121.1:p.Ser965Ala
XM_011542820.1:c.2881T>G	XP_011541122.1:p.Ser961Ala
XM_011542821.1:c.2773T>G	XP_011541123.1:p.Ser925Ala
XM_011542824.1:c.2011T>G	XP_011541126.1:p.Ser671Ala
XM_011542825.1:c.1168T>G	XP_011541127.1:p.Ser390Ala
XM_011542826.1:c.1033T>G	XP_011541128.1:p.Ser345Ala
XM_011542827.1:c.913T>G	XP_011541129.1:p.Ser305Ala
NM_001347918.1:c.2527T>G	NP_001334847.1:p.Ser843Ala
NM_001347919.1:c.2574-1022T>G	NP_001334848.1:n.2574-1022T>G
NM_001347922.1:c.976T>G	NP_001334851.1:p.Ser326Ala
NM_001347923.1:c.922T>G	NP_001334852.1:p.Ser308Ala
NM_001347924.1:c.667T>G	NP_001334853.1:p.Ser223Ala
NM_001347925.1:c.613T>G	NP_001334854.1:p.Ser205Ala
NM_001347926.1:c.714-1022T>G	NP_001334855.1:n.714-1022T>G
NM_001347927.1:c.367T>G	NP_001334856.1:p.Ser123Ala
NR_144939.1:n.3280T>G
XM_011542820.2:c.2881T>G	XP_011541122.1:p.Ser961Ala
XM_011542821.3:c.2773T>G	XP_011541123.1:p.Ser925Ala
XM_011542824.2:c.2011T>G	XP_011541126.1:p.Ser671Ala
XM_011542825.2:c.1168T>G	XP_011541127.1:p.Ser390Ala
XM_011542826.2:c.1033T>G	XP_011541128.1:p.Ser345Ala
XM_024448521.1:c.2893T>G	XP_024304289.1:p.Ser965Ala
XR_001747870.1:n.3718T>G
XR_001747872.1:n.3064T>G
XR_001747873.1:n.3378T>G
NM_001301089.2:c.787T>G	NP_001288018.1:p.Ser263Ala
NM_001347918.2:c.2527T>G	NP_001334847.2:p.Ser843Ala
NM_001347919.2:c.2574-1022T>G	NP_001334848.2:n.2574-1022T>G
NM_001347920.2:c.*21043T>G	NP_001334849.2:n.*21043T>G
NM_001347922.2:c.976T>G	NP_001334851.2:p.Ser326Ala
NM_001347923.2:c.922T>G	NP_001334852.2:p.Ser308Ala
NM_001347924.2:c.667T>G	NP_001334853.1:p.Ser223Ala
NM_001347925.2:c.613T>G	NP_001334854.1:p.Ser205Ala
NM_001347926.2:c.714-1022T>G	NP_001334855.1:n.714-1022T>G
NM_001347927.2:c.367T>G	NP_001334856.1:p.Ser123Ala
NM_014758.3:c.2647T>G MANE Select	NP_055573.3:p.Ser883Ala
NR_144939.2:n.3272T>G