Canonical Allele Identifier: CA383457751

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750600T>C (hg19) ; chr11:g.130880705T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880705T>C , CM000673.2:g.130880705T>C	GRCh38
NC_000011.9:g.130750600T>C , CM000673.1:g.130750600T>C	GRCh37
NC_000011.8:g.130255810T>C	NCBI36
NG_053190.1:g.40784A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2675A>G MANE Select	ENSP00000265909.4:p.Lys892Arg
ENST00000265909.8:c.2675A>G	ENSP00000265909.4:p.Lys892Arg
ENST00000426933.6:c.179A>G	ENSP00000413345.2:p.Lys60Arg
ENST00000526579.5:n.178-994A>G
ENST00000527116.5:n.437A>G
ENST00000528555.5:c.815A>G	ENSP00000435122.1:p.Lys272Arg
ENST00000530330.1:n.411A>G
ENST00000530356.5:c.815A>G	ENSP00000432307.1:p.Lys272Arg
ENST00000533318.5:n.1035A>G
ENST00000534726.5:c.395A>G	ENSP00000433699.1:p.Lys132Arg
NM_001301089.1:c.815A>G	NP_001288018.1:p.Lys272Arg
NM_014758.2:c.2675A>G	NP_055573.2:p.Lys892Arg
XM_005271546.3:c.2574-994A>G	XP_005271603.1:n.2574-994A>G
XM_011542819.1:c.2921A>G	XP_011541121.1:p.Lys974Arg
XM_011542820.1:c.2909A>G	XP_011541122.1:p.Lys970Arg
XM_011542821.1:c.2801A>G	XP_011541123.1:p.Lys934Arg
XM_011542824.1:c.2039A>G	XP_011541126.1:p.Lys680Arg
XM_011542825.1:c.1196A>G	XP_011541127.1:p.Lys399Arg
XM_011542826.1:c.1061A>G	XP_011541128.1:p.Lys354Arg
XM_011542827.1:c.941A>G	XP_011541129.1:p.Lys314Arg
NM_001347918.1:c.2555A>G	NP_001334847.1:p.Lys852Arg
NM_001347919.1:c.2574-994A>G	NP_001334848.1:n.2574-994A>G
NM_001347922.1:c.1004A>G	NP_001334851.1:p.Lys335Arg
NM_001347923.1:c.950A>G	NP_001334852.1:p.Lys317Arg
NM_001347924.1:c.695A>G	NP_001334853.1:p.Lys232Arg
NM_001347925.1:c.641A>G	NP_001334854.1:p.Lys214Arg
NM_001347926.1:c.714-994A>G	NP_001334855.1:n.714-994A>G
NM_001347927.1:c.395A>G	NP_001334856.1:p.Lys132Arg
NR_144939.1:n.3308A>G
XM_011542820.2:c.2909A>G	XP_011541122.1:p.Lys970Arg
XM_011542821.3:c.2801A>G	XP_011541123.1:p.Lys934Arg
XM_011542824.2:c.2039A>G	XP_011541126.1:p.Lys680Arg
XM_011542825.2:c.1196A>G	XP_011541127.1:p.Lys399Arg
XM_011542826.2:c.1061A>G	XP_011541128.1:p.Lys354Arg
XM_024448521.1:c.2921A>G	XP_024304289.1:p.Lys974Arg
XR_001747870.1:n.3746A>G
XR_001747872.1:n.3092A>G
XR_001747873.1:n.3406A>G
NM_001301089.2:c.815A>G	NP_001288018.1:p.Lys272Arg
NM_001347918.2:c.2555A>G	NP_001334847.2:p.Lys852Arg
NM_001347919.2:c.2574-994A>G	NP_001334848.2:n.2574-994A>G
NM_001347920.2:c.*21071A>G	NP_001334849.2:n.*21071A>G
NM_001347922.2:c.1004A>G	NP_001334851.2:p.Lys335Arg
NM_001347923.2:c.950A>G	NP_001334852.2:p.Lys317Arg
NM_001347924.2:c.695A>G	NP_001334853.1:p.Lys232Arg
NM_001347925.2:c.641A>G	NP_001334854.1:p.Lys214Arg
NM_001347926.2:c.714-994A>G	NP_001334855.1:n.714-994A>G
NM_001347927.2:c.395A>G	NP_001334856.1:p.Lys132Arg
NM_014758.3:c.2675A>G MANE Select	NP_055573.3:p.Lys892Arg
NR_144939.2:n.3300A>G