Canonical Allele Identifier: CA383457673

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750562C>A (hg19) ; chr11:g.130880667C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880667C>A , CM000673.2:g.130880667C>A	GRCh38
NC_000011.9:g.130750562C>A , CM000673.1:g.130750562C>A	GRCh37
NC_000011.8:g.130255772C>A	NCBI36
NG_053190.1:g.40822G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2713G>T MANE Select	ENSP00000265909.4:p.Ala905Ser
ENST00000265909.8:c.2713G>T	ENSP00000265909.4:p.Ala905Ser
ENST00000426933.6:c.217G>T	ENSP00000413345.2:p.Ala73Ser
ENST00000526579.5:n.178-956G>T
ENST00000527116.5:n.475G>T
ENST00000528555.5:c.853G>T	ENSP00000435122.1:p.Ala285Ser
ENST00000530330.1:n.449G>T
ENST00000530356.5:c.853G>T	ENSP00000432307.1:p.Ala285Ser
ENST00000533318.5:n.1073G>T
ENST00000534726.5:c.433G>T	ENSP00000433699.1:p.Ala145Ser
NM_001301089.1:c.853G>T	NP_001288018.1:p.Ala285Ser
NM_014758.2:c.2713G>T	NP_055573.2:p.Ala905Ser
XM_005271546.3:c.2574-956G>T	XP_005271603.1:n.2574-956G>T
XM_011542819.1:c.2959G>T	XP_011541121.1:p.Ala987Ser
XM_011542820.1:c.2947G>T	XP_011541122.1:p.Ala983Ser
XM_011542821.1:c.2839G>T	XP_011541123.1:p.Ala947Ser
XM_011542824.1:c.2077G>T	XP_011541126.1:p.Ala693Ser
XM_011542825.1:c.1234G>T	XP_011541127.1:p.Ala412Ser
XM_011542826.1:c.1099G>T	XP_011541128.1:p.Ala367Ser
XM_011542827.1:c.979G>T	XP_011541129.1:p.Ala327Ser
NM_001347918.1:c.2593G>T	NP_001334847.1:p.Ala865Ser
NM_001347919.1:c.2574-956G>T	NP_001334848.1:n.2574-956G>T
NM_001347922.1:c.1042G>T	NP_001334851.1:p.Ala348Ser
NM_001347923.1:c.988G>T	NP_001334852.1:p.Ala330Ser
NM_001347924.1:c.733G>T	NP_001334853.1:p.Ala245Ser
NM_001347925.1:c.679G>T	NP_001334854.1:p.Ala227Ser
NM_001347926.1:c.714-956G>T	NP_001334855.1:n.714-956G>T
NM_001347927.1:c.433G>T	NP_001334856.1:p.Ala145Ser
NR_144939.1:n.3346G>T
XM_011542820.2:c.2947G>T	XP_011541122.1:p.Ala983Ser
XM_011542821.3:c.2839G>T	XP_011541123.1:p.Ala947Ser
XM_011542824.2:c.2077G>T	XP_011541126.1:p.Ala693Ser
XM_011542825.2:c.1234G>T	XP_011541127.1:p.Ala412Ser
XM_011542826.2:c.1099G>T	XP_011541128.1:p.Ala367Ser
XM_024448521.1:c.2959G>T	XP_024304289.1:p.Ala987Ser
XR_001747870.1:n.3784G>T
XR_001747872.1:n.3130G>T
XR_001747873.1:n.3444G>T
NM_001301089.2:c.853G>T	NP_001288018.1:p.Ala285Ser
NM_001347918.2:c.2593G>T	NP_001334847.2:p.Ala865Ser
NM_001347919.2:c.2574-956G>T	NP_001334848.2:n.2574-956G>T
NM_001347920.2:c.*21109G>T	NP_001334849.2:n.*21109G>T
NM_001347922.2:c.1042G>T	NP_001334851.2:p.Ala348Ser
NM_001347923.2:c.988G>T	NP_001334852.2:p.Ala330Ser
NM_001347924.2:c.733G>T	NP_001334853.1:p.Ala245Ser
NM_001347925.2:c.679G>T	NP_001334854.1:p.Ala227Ser
NM_001347926.2:c.714-956G>T	NP_001334855.1:n.714-956G>T
NM_001347927.2:c.433G>T	NP_001334856.1:p.Ala145Ser
NM_014758.3:c.2713G>T MANE Select	NP_055573.3:p.Ala905Ser
NR_144939.2:n.3338G>T