Canonical Allele Identifier: CA383457578

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750520G>C (hg19) ; chr11:g.130880625G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880625G>C , CM000673.2:g.130880625G>C	GRCh38
NC_000011.9:g.130750520G>C , CM000673.1:g.130750520G>C	GRCh37
NC_000011.8:g.130255730G>C	NCBI36
NG_053190.1:g.40864C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2755C>G MANE Select	ENSP00000265909.4:p.Pro919Ala
ENST00000265909.8:c.2755C>G	ENSP00000265909.4:p.Pro919Ala
ENST00000426933.6:c.259C>G	ENSP00000413345.2:p.Pro87Ala
ENST00000526579.5:n.178-914C>G
ENST00000527116.5:n.517C>G
ENST00000528555.5:c.895C>G	ENSP00000435122.1:p.Pro299Ala
ENST00000530330.1:n.491C>G
ENST00000530356.5:c.895C>G	ENSP00000432307.1:p.Pro299Ala
ENST00000533318.5:n.1115C>G
ENST00000534726.5:c.475C>G	ENSP00000433699.1:p.Pro159Ala
NM_001301089.1:c.895C>G	NP_001288018.1:p.Pro299Ala
NM_014758.2:c.2755C>G	NP_055573.2:p.Pro919Ala
XM_005271546.3:c.2574-914C>G	XP_005271603.1:n.2574-914C>G
XM_011542819.1:c.3001C>G	XP_011541121.1:p.Pro1001Ala
XM_011542820.1:c.2989C>G	XP_011541122.1:p.Pro997Ala
XM_011542821.1:c.2881C>G	XP_011541123.1:p.Pro961Ala
XM_011542824.1:c.2119C>G	XP_011541126.1:p.Pro707Ala
XM_011542825.1:c.1276C>G	XP_011541127.1:p.Pro426Ala
XM_011542826.1:c.1141C>G	XP_011541128.1:p.Pro381Ala
XM_011542827.1:c.1021C>G	XP_011541129.1:p.Pro341Ala
NM_001347918.1:c.2635C>G	NP_001334847.1:p.Pro879Ala
NM_001347919.1:c.2574-914C>G	NP_001334848.1:n.2574-914C>G
NM_001347922.1:c.1084C>G	NP_001334851.1:p.Pro362Ala
NM_001347923.1:c.1030C>G	NP_001334852.1:p.Pro344Ala
NM_001347924.1:c.775C>G	NP_001334853.1:p.Pro259Ala
NM_001347925.1:c.721C>G	NP_001334854.1:p.Pro241Ala
NM_001347926.1:c.714-914C>G	NP_001334855.1:n.714-914C>G
NM_001347927.1:c.475C>G	NP_001334856.1:p.Pro159Ala
NR_144939.1:n.3388C>G
XM_011542820.2:c.2989C>G	XP_011541122.1:p.Pro997Ala
XM_011542821.3:c.2881C>G	XP_011541123.1:p.Pro961Ala
XM_011542824.2:c.2119C>G	XP_011541126.1:p.Pro707Ala
XM_011542825.2:c.1276C>G	XP_011541127.1:p.Pro426Ala
XM_011542826.2:c.1141C>G	XP_011541128.1:p.Pro381Ala
XM_024448521.1:c.3001C>G	XP_024304289.1:p.Pro1001Ala
XR_001747870.1:n.3826C>G
XR_001747872.1:n.3172C>G
XR_001747873.1:n.3486C>G
NM_001301089.2:c.895C>G	NP_001288018.1:p.Pro299Ala
NM_001347918.2:c.2635C>G	NP_001334847.2:p.Pro879Ala
NM_001347919.2:c.2574-914C>G	NP_001334848.2:n.2574-914C>G
NM_001347920.2:c.*21151C>G	NP_001334849.2:n.*21151C>G
NM_001347922.2:c.1084C>G	NP_001334851.2:p.Pro362Ala
NM_001347923.2:c.1030C>G	NP_001334852.2:p.Pro344Ala
NM_001347924.2:c.775C>G	NP_001334853.1:p.Pro259Ala
NM_001347925.2:c.721C>G	NP_001334854.1:p.Pro241Ala
NM_001347926.2:c.714-914C>G	NP_001334855.1:n.714-914C>G
NM_001347927.2:c.475C>G	NP_001334856.1:p.Pro159Ala
NM_014758.3:c.2755C>G MANE Select	NP_055573.3:p.Pro919Ala
NR_144939.2:n.3380C>G