Canonical Allele Identifier: CA477582267

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750560A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880665A>C , CM000673.2:g.130880665A>C	GRCh38
NC_000011.9:g.130750560A>C , CM000673.1:g.130750560A>C	GRCh37
NC_000011.8:g.130255770A>C	NCBI36
NG_053190.1:g.40824T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2715T>G MANE Select	ENSP00000265909.4:p.Ala905=
ENST00000265909.8:c.2715T>G	ENSP00000265909.4:p.Ala905=
ENST00000426933.6:c.219T>G	ENSP00000413345.2:p.Ala73=
ENST00000526579.5:n.178-954T>G
ENST00000527116.5:n.477T>G
ENST00000528555.5:c.855T>G	ENSP00000435122.1:p.Ala285=
ENST00000530330.1:n.451T>G
ENST00000530356.5:c.855T>G	ENSP00000432307.1:p.Ala285=
ENST00000533318.5:n.1075T>G
ENST00000534726.5:c.435T>G	ENSP00000433699.1:p.Ala145=
NM_001301089.1:c.855T>G	NP_001288018.1:p.Ala285=
NM_014758.2:c.2715T>G	NP_055573.2:p.Ala905=
XM_005271546.3:c.2574-954T>G	XP_005271603.1:n.2574-954T>G
XM_011542819.1:c.2961T>G	XP_011541121.1:p.Ala987=
XM_011542820.1:c.2949T>G	XP_011541122.1:p.Ala983=
XM_011542821.1:c.2841T>G	XP_011541123.1:p.Ala947=
XM_011542824.1:c.2079T>G	XP_011541126.1:p.Ala693=
XM_011542825.1:c.1236T>G	XP_011541127.1:p.Ala412=
XM_011542826.1:c.1101T>G	XP_011541128.1:p.Ala367=
XM_011542827.1:c.981T>G	XP_011541129.1:p.Ala327=
NM_001347918.1:c.2595T>G	NP_001334847.1:p.Ala865=
NM_001347919.1:c.2574-954T>G	NP_001334848.1:n.2574-954T>G
NM_001347922.1:c.1044T>G	NP_001334851.1:p.Ala348=
NM_001347923.1:c.990T>G	NP_001334852.1:p.Ala330=
NM_001347924.1:c.735T>G	NP_001334853.1:p.Ala245=
NM_001347925.1:c.681T>G	NP_001334854.1:p.Ala227=
NM_001347926.1:c.714-954T>G	NP_001334855.1:n.714-954T>G
NM_001347927.1:c.435T>G	NP_001334856.1:p.Ala145=
NR_144939.1:n.3348T>G
XM_011542820.2:c.2949T>G	XP_011541122.1:p.Ala983=
XM_011542821.3:c.2841T>G	XP_011541123.1:p.Ala947=
XM_011542824.2:c.2079T>G	XP_011541126.1:p.Ala693=
XM_011542825.2:c.1236T>G	XP_011541127.1:p.Ala412=
XM_011542826.2:c.1101T>G	XP_011541128.1:p.Ala367=
XM_024448521.1:c.2961T>G	XP_024304289.1:p.Ala987=
XR_001747870.1:n.3786T>G
XR_001747872.1:n.3132T>G
XR_001747873.1:n.3446T>G
NM_001301089.2:c.855T>G	NP_001288018.1:p.Ala285=
NM_001347918.2:c.2595T>G	NP_001334847.2:p.Ala865=
NM_001347919.2:c.2574-954T>G	NP_001334848.2:n.2574-954T>G
NM_001347920.2:c.*21111T>G	NP_001334849.2:n.*21111T>G
NM_001347922.2:c.1044T>G	NP_001334851.2:p.Ala348=
NM_001347923.2:c.990T>G	NP_001334852.2:p.Ala330=
NM_001347924.2:c.735T>G	NP_001334853.1:p.Ala245=
NM_001347925.2:c.681T>G	NP_001334854.1:p.Ala227=
NM_001347926.2:c.714-954T>G	NP_001334855.1:n.714-954T>G
NM_001347927.2:c.435T>G	NP_001334856.1:p.Ala145=
NM_014758.3:c.2715T>G MANE Select	NP_055573.3:p.Ala905=
NR_144939.2:n.3340T>G