Canonical Allele Identifier: CA383457575

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750519G>C (hg19) ; chr11:g.130880624G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880624G>C , CM000673.2:g.130880624G>C	GRCh38
NC_000011.9:g.130750519G>C , CM000673.1:g.130750519G>C	GRCh37
NC_000011.8:g.130255729G>C	NCBI36
NG_053190.1:g.40865C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2756C>G MANE Select	ENSP00000265909.4:p.Pro919Arg
ENST00000265909.8:c.2756C>G	ENSP00000265909.4:p.Pro919Arg
ENST00000426933.6:c.260C>G	ENSP00000413345.2:p.Pro87Arg
ENST00000526579.5:n.178-913C>G
ENST00000527116.5:n.518C>G
ENST00000528555.5:c.896C>G	ENSP00000435122.1:p.Pro299Arg
ENST00000530330.1:n.492C>G
ENST00000530356.5:c.896C>G	ENSP00000432307.1:p.Pro299Arg
ENST00000533318.5:n.1116C>G
ENST00000534726.5:c.476C>G	ENSP00000433699.1:p.Pro159Arg
NM_001301089.1:c.896C>G	NP_001288018.1:p.Pro299Arg
NM_014758.2:c.2756C>G	NP_055573.2:p.Pro919Arg
XM_005271546.3:c.2574-913C>G	XP_005271603.1:n.2574-913C>G
XM_011542819.1:c.3002C>G	XP_011541121.1:p.Pro1001Arg
XM_011542820.1:c.2990C>G	XP_011541122.1:p.Pro997Arg
XM_011542821.1:c.2882C>G	XP_011541123.1:p.Pro961Arg
XM_011542824.1:c.2120C>G	XP_011541126.1:p.Pro707Arg
XM_011542825.1:c.1277C>G	XP_011541127.1:p.Pro426Arg
XM_011542826.1:c.1142C>G	XP_011541128.1:p.Pro381Arg
XM_011542827.1:c.1022C>G	XP_011541129.1:p.Pro341Arg
NM_001347918.1:c.2636C>G	NP_001334847.1:p.Pro879Arg
NM_001347919.1:c.2574-913C>G	NP_001334848.1:n.2574-913C>G
NM_001347922.1:c.1085C>G	NP_001334851.1:p.Pro362Arg
NM_001347923.1:c.1031C>G	NP_001334852.1:p.Pro344Arg
NM_001347924.1:c.776C>G	NP_001334853.1:p.Pro259Arg
NM_001347925.1:c.722C>G	NP_001334854.1:p.Pro241Arg
NM_001347926.1:c.714-913C>G	NP_001334855.1:n.714-913C>G
NM_001347927.1:c.476C>G	NP_001334856.1:p.Pro159Arg
NR_144939.1:n.3389C>G
XM_011542820.2:c.2990C>G	XP_011541122.1:p.Pro997Arg
XM_011542821.3:c.2882C>G	XP_011541123.1:p.Pro961Arg
XM_011542824.2:c.2120C>G	XP_011541126.1:p.Pro707Arg
XM_011542825.2:c.1277C>G	XP_011541127.1:p.Pro426Arg
XM_011542826.2:c.1142C>G	XP_011541128.1:p.Pro381Arg
XM_024448521.1:c.3002C>G	XP_024304289.1:p.Pro1001Arg
XR_001747870.1:n.3827C>G
XR_001747872.1:n.3173C>G
XR_001747873.1:n.3487C>G
NM_001301089.2:c.896C>G	NP_001288018.1:p.Pro299Arg
NM_001347918.2:c.2636C>G	NP_001334847.2:p.Pro879Arg
NM_001347919.2:c.2574-913C>G	NP_001334848.2:n.2574-913C>G
NM_001347920.2:c.*21152C>G	NP_001334849.2:n.*21152C>G
NM_001347922.2:c.1085C>G	NP_001334851.2:p.Pro362Arg
NM_001347923.2:c.1031C>G	NP_001334852.2:p.Pro344Arg
NM_001347924.2:c.776C>G	NP_001334853.1:p.Pro259Arg
NM_001347925.2:c.722C>G	NP_001334854.1:p.Pro241Arg
NM_001347926.2:c.714-913C>G	NP_001334855.1:n.714-913C>G
NM_001347927.2:c.476C>G	NP_001334856.1:p.Pro159Arg
NM_014758.3:c.2756C>G MANE Select	NP_055573.3:p.Pro919Arg
NR_144939.2:n.3381C>G