Canonical Allele Identifier: CA230763279

Gene: SNX19

Linked Data

• dbSNP Id: rs376835065
• gnomAD v2: 11-130750651-T-C
• gnomAD v4: 11-130880756-T-C
• MyVariant Identifiers: chr11:g.130750651T>C (hg19) ; chr11:g.130880756T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880756T>C , CM000673.2:g.130880756T>C	GRCh38
NC_000011.9:g.130750651T>C , CM000673.1:g.130750651T>C	GRCh37
NC_000011.8:g.130255861T>C	NCBI36
NG_053190.1:g.40733A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265909.9:c.2624A>G MANE Select	ENSP00000265909.4:p.Gln875Arg
ENST00000265909.8:c.2624A>G	ENSP00000265909.4:p.Gln875Arg
ENST00000426933.6:c.128A>G	ENSP00000413345.2:p.Gln43Arg
ENST00000526579.5:n.178-1045A>G
ENST00000527116.5:n.386A>G
ENST00000528555.5:c.764A>G	ENSP00000435122.1:p.Gln255Arg
ENST00000530330.1:n.360A>G
ENST00000530356.5:c.764A>G	ENSP00000432307.1:p.Gln255Arg
ENST00000533318.5:n.984A>G
ENST00000534726.5:c.344A>G	ENSP00000433699.1:p.Gln115Arg
NM_001301089.1:c.764A>G	NP_001288018.1:p.Gln255Arg
NM_014758.2:c.2624A>G	NP_055573.2:p.Gln875Arg
XM_005271546.3:c.2574-1045A>G	XP_005271603.1:n.2574-1045A>G
XM_011542819.1:c.2870A>G	XP_011541121.1:p.Gln957Arg
XM_011542820.1:c.2858A>G	XP_011541122.1:p.Gln953Arg
XM_011542821.1:c.2750A>G	XP_011541123.1:p.Gln917Arg
XM_011542824.1:c.1988A>G	XP_011541126.1:p.Gln663Arg
XM_011542825.1:c.1145A>G	XP_011541127.1:p.Gln382Arg
XM_011542826.1:c.1010A>G	XP_011541128.1:p.Gln337Arg
XM_011542827.1:c.890A>G	XP_011541129.1:p.Gln297Arg
NM_001347918.1:c.2504A>G	NP_001334847.1:p.Gln835Arg
NM_001347919.1:c.2574-1045A>G	NP_001334848.1:n.2574-1045A>G
NM_001347922.1:c.953A>G	NP_001334851.1:p.Gln318Arg
NM_001347923.1:c.899A>G	NP_001334852.1:p.Gln300Arg
NM_001347924.1:c.644A>G	NP_001334853.1:p.Gln215Arg
NM_001347925.1:c.590A>G	NP_001334854.1:p.Gln197Arg
NM_001347926.1:c.714-1045A>G	NP_001334855.1:n.714-1045A>G
NM_001347927.1:c.344A>G	NP_001334856.1:p.Gln115Arg
NR_144939.1:n.3257A>G
XM_011542820.2:c.2858A>G	XP_011541122.1:p.Gln953Arg
XM_011542821.3:c.2750A>G	XP_011541123.1:p.Gln917Arg
XM_011542824.2:c.1988A>G	XP_011541126.1:p.Gln663Arg
XM_011542825.2:c.1145A>G	XP_011541127.1:p.Gln382Arg
XM_011542826.2:c.1010A>G	XP_011541128.1:p.Gln337Arg
XM_024448521.1:c.2870A>G	XP_024304289.1:p.Gln957Arg
XR_001747870.1:n.3695A>G
XR_001747872.1:n.3041A>G
XR_001747873.1:n.3355A>G
NM_001301089.2:c.764A>G	NP_001288018.1:p.Gln255Arg
NM_001347918.2:c.2504A>G	NP_001334847.2:p.Gln835Arg
NM_001347919.2:c.2574-1045A>G	NP_001334848.2:n.2574-1045A>G
NM_001347920.2:c.*21020A>G	NP_001334849.2:n.*21020A>G
NM_001347922.2:c.953A>G	NP_001334851.2:p.Gln318Arg
NM_001347923.2:c.899A>G	NP_001334852.2:p.Gln300Arg
NM_001347924.2:c.644A>G	NP_001334853.1:p.Gln215Arg
NM_001347925.2:c.590A>G	NP_001334854.1:p.Gln197Arg
NM_001347926.2:c.714-1045A>G	NP_001334855.1:n.714-1045A>G
NM_001347927.2:c.344A>G	NP_001334856.1:p.Gln115Arg
NM_014758.3:c.2624A>G MANE Select	NP_055573.3:p.Gln875Arg
NR_144939.2:n.3249A>G