Canonical Allele Identifier: CA477582309

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750614A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880719A>T , CM000673.2:g.130880719A>T	GRCh38
NC_000011.9:g.130750614A>T , CM000673.1:g.130750614A>T	GRCh37
NC_000011.8:g.130255824A>T	NCBI36
NG_053190.1:g.40770T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2661T>A MANE Select	ENSP00000265909.4:p.Gly887=
ENST00000265909.8:c.2661T>A	ENSP00000265909.4:p.Gly887=
ENST00000426933.6:c.165T>A	ENSP00000413345.2:p.Gly55=
ENST00000526579.5:n.178-1008T>A
ENST00000527116.5:n.423T>A
ENST00000528555.5:c.801T>A	ENSP00000435122.1:p.Gly267=
ENST00000530330.1:n.397T>A
ENST00000530356.5:c.801T>A	ENSP00000432307.1:p.Gly267=
ENST00000533318.5:n.1021T>A
ENST00000534726.5:c.381T>A	ENSP00000433699.1:p.Gly127=
NM_001301089.1:c.801T>A	NP_001288018.1:p.Gly267=
NM_014758.2:c.2661T>A	NP_055573.2:p.Gly887=
XM_005271546.3:c.2574-1008T>A	XP_005271603.1:n.2574-1008T>A
XM_011542819.1:c.2907T>A	XP_011541121.1:p.Gly969=
XM_011542820.1:c.2895T>A	XP_011541122.1:p.Gly965=
XM_011542821.1:c.2787T>A	XP_011541123.1:p.Gly929=
XM_011542824.1:c.2025T>A	XP_011541126.1:p.Gly675=
XM_011542825.1:c.1182T>A	XP_011541127.1:p.Gly394=
XM_011542826.1:c.1047T>A	XP_011541128.1:p.Gly349=
XM_011542827.1:c.927T>A	XP_011541129.1:p.Gly309=
NM_001347918.1:c.2541T>A	NP_001334847.1:p.Gly847=
NM_001347919.1:c.2574-1008T>A	NP_001334848.1:n.2574-1008T>A
NM_001347922.1:c.990T>A	NP_001334851.1:p.Gly330=
NM_001347923.1:c.936T>A	NP_001334852.1:p.Gly312=
NM_001347924.1:c.681T>A	NP_001334853.1:p.Gly227=
NM_001347925.1:c.627T>A	NP_001334854.1:p.Gly209=
NM_001347926.1:c.714-1008T>A	NP_001334855.1:n.714-1008T>A
NM_001347927.1:c.381T>A	NP_001334856.1:p.Gly127=
NR_144939.1:n.3294T>A
XM_011542820.2:c.2895T>A	XP_011541122.1:p.Gly965=
XM_011542821.3:c.2787T>A	XP_011541123.1:p.Gly929=
XM_011542824.2:c.2025T>A	XP_011541126.1:p.Gly675=
XM_011542825.2:c.1182T>A	XP_011541127.1:p.Gly394=
XM_011542826.2:c.1047T>A	XP_011541128.1:p.Gly349=
XM_024448521.1:c.2907T>A	XP_024304289.1:p.Gly969=
XR_001747870.1:n.3732T>A
XR_001747872.1:n.3078T>A
XR_001747873.1:n.3392T>A
NM_001301089.2:c.801T>A	NP_001288018.1:p.Gly267=
NM_001347918.2:c.2541T>A	NP_001334847.2:p.Gly847=
NM_001347919.2:c.2574-1008T>A	NP_001334848.2:n.2574-1008T>A
NM_001347920.2:c.*21057T>A	NP_001334849.2:n.*21057T>A
NM_001347922.2:c.990T>A	NP_001334851.2:p.Gly330=
NM_001347923.2:c.936T>A	NP_001334852.2:p.Gly312=
NM_001347924.2:c.681T>A	NP_001334853.1:p.Gly227=
NM_001347925.2:c.627T>A	NP_001334854.1:p.Gly209=
NM_001347926.2:c.714-1008T>A	NP_001334855.1:n.714-1008T>A
NM_001347927.2:c.381T>A	NP_001334856.1:p.Gly127=
NM_014758.3:c.2661T>A MANE Select	NP_055573.3:p.Gly887=
NR_144939.2:n.3286T>A