Canonical Allele Identifier: CA477582294

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750596A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880701A>G , CM000673.2:g.130880701A>G	GRCh38
NC_000011.9:g.130750596A>G , CM000673.1:g.130750596A>G	GRCh37
NC_000011.8:g.130255806A>G	NCBI36
NG_053190.1:g.40788T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2679T>C MANE Select	ENSP00000265909.4:p.Phe893=
ENST00000265909.8:c.2679T>C	ENSP00000265909.4:p.Phe893=
ENST00000426933.6:c.183T>C	ENSP00000413345.2:p.Phe61=
ENST00000526579.5:n.178-990T>C
ENST00000527116.5:n.441T>C
ENST00000528555.5:c.819T>C	ENSP00000435122.1:p.Phe273=
ENST00000530330.1:n.415T>C
ENST00000530356.5:c.819T>C	ENSP00000432307.1:p.Phe273=
ENST00000533318.5:n.1039T>C
ENST00000534726.5:c.399T>C	ENSP00000433699.1:p.Phe133=
NM_001301089.1:c.819T>C	NP_001288018.1:p.Phe273=
NM_014758.2:c.2679T>C	NP_055573.2:p.Phe893=
XM_005271546.3:c.2574-990T>C	XP_005271603.1:n.2574-990T>C
XM_011542819.1:c.2925T>C	XP_011541121.1:p.Phe975=
XM_011542820.1:c.2913T>C	XP_011541122.1:p.Phe971=
XM_011542821.1:c.2805T>C	XP_011541123.1:p.Phe935=
XM_011542824.1:c.2043T>C	XP_011541126.1:p.Phe681=
XM_011542825.1:c.1200T>C	XP_011541127.1:p.Phe400=
XM_011542826.1:c.1065T>C	XP_011541128.1:p.Phe355=
XM_011542827.1:c.945T>C	XP_011541129.1:p.Phe315=
NM_001347918.1:c.2559T>C	NP_001334847.1:p.Phe853=
NM_001347919.1:c.2574-990T>C	NP_001334848.1:n.2574-990T>C
NM_001347922.1:c.1008T>C	NP_001334851.1:p.Phe336=
NM_001347923.1:c.954T>C	NP_001334852.1:p.Phe318=
NM_001347924.1:c.699T>C	NP_001334853.1:p.Phe233=
NM_001347925.1:c.645T>C	NP_001334854.1:p.Phe215=
NM_001347926.1:c.714-990T>C	NP_001334855.1:n.714-990T>C
NM_001347927.1:c.399T>C	NP_001334856.1:p.Phe133=
NR_144939.1:n.3312T>C
XM_011542820.2:c.2913T>C	XP_011541122.1:p.Phe971=
XM_011542821.3:c.2805T>C	XP_011541123.1:p.Phe935=
XM_011542824.2:c.2043T>C	XP_011541126.1:p.Phe681=
XM_011542825.2:c.1200T>C	XP_011541127.1:p.Phe400=
XM_011542826.2:c.1065T>C	XP_011541128.1:p.Phe355=
XM_024448521.1:c.2925T>C	XP_024304289.1:p.Phe975=
XR_001747870.1:n.3750T>C
XR_001747872.1:n.3096T>C
XR_001747873.1:n.3410T>C
NM_001301089.2:c.819T>C	NP_001288018.1:p.Phe273=
NM_001347918.2:c.2559T>C	NP_001334847.2:p.Phe853=
NM_001347919.2:c.2574-990T>C	NP_001334848.2:n.2574-990T>C
NM_001347920.2:c.*21075T>C	NP_001334849.2:n.*21075T>C
NM_001347922.2:c.1008T>C	NP_001334851.2:p.Phe336=
NM_001347923.2:c.954T>C	NP_001334852.2:p.Phe318=
NM_001347924.2:c.699T>C	NP_001334853.1:p.Phe233=
NM_001347925.2:c.645T>C	NP_001334854.1:p.Phe215=
NM_001347926.2:c.714-990T>C	NP_001334855.1:n.714-990T>C
NM_001347927.2:c.399T>C	NP_001334856.1:p.Phe133=
NM_014758.3:c.2679T>C MANE Select	NP_055573.3:p.Phe893=
NR_144939.2:n.3304T>C