Canonical Allele Identifier: CA230763218

Gene: SNX19

Linked Data

• dbSNP Id: rs1037731153
• gnomAD v2: 11-130750571-G-A
• gnomAD v4: 11-130880676-G-A
• COSMIC: COSM3967421
• MyVariant Identifiers: chr11:g.130750571G>A (hg19) ; chr11:g.130880676G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880676G>A , CM000673.2:g.130880676G>A	GRCh38
NC_000011.9:g.130750571G>A , CM000673.1:g.130750571G>A	GRCh37
NC_000011.8:g.130255781G>A	NCBI36
NG_053190.1:g.40813C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2704C>T MANE Select	ENSP00000265909.4:p.Gln902Ter
ENST00000265909.8:c.2704C>T	ENSP00000265909.4:p.Gln902Ter
ENST00000426933.6:c.208C>T	ENSP00000413345.2:p.Gln70Ter
ENST00000526579.5:n.178-965C>T
ENST00000527116.5:n.466C>T
ENST00000528555.5:c.844C>T	ENSP00000435122.1:p.Gln282Ter
ENST00000530330.1:n.440C>T
ENST00000530356.5:c.844C>T	ENSP00000432307.1:p.Gln282Ter
ENST00000533318.5:n.1064C>T
ENST00000534726.5:c.424C>T	ENSP00000433699.1:p.Gln142Ter
NM_001301089.1:c.844C>T	NP_001288018.1:p.Gln282Ter
NM_014758.2:c.2704C>T	NP_055573.2:p.Gln902Ter
XM_005271546.3:c.2574-965C>T	XP_005271603.1:n.2574-965C>T
XM_011542819.1:c.2950C>T	XP_011541121.1:p.Gln984Ter
XM_011542820.1:c.2938C>T	XP_011541122.1:p.Gln980Ter
XM_011542821.1:c.2830C>T	XP_011541123.1:p.Gln944Ter
XM_011542824.1:c.2068C>T	XP_011541126.1:p.Gln690Ter
XM_011542825.1:c.1225C>T	XP_011541127.1:p.Gln409Ter
XM_011542826.1:c.1090C>T	XP_011541128.1:p.Gln364Ter
XM_011542827.1:c.970C>T	XP_011541129.1:p.Gln324Ter
NM_001347918.1:c.2584C>T	NP_001334847.1:p.Gln862Ter
NM_001347919.1:c.2574-965C>T	NP_001334848.1:n.2574-965C>T
NM_001347922.1:c.1033C>T	NP_001334851.1:p.Gln345Ter
NM_001347923.1:c.979C>T	NP_001334852.1:p.Gln327Ter
NM_001347924.1:c.724C>T	NP_001334853.1:p.Gln242Ter
NM_001347925.1:c.670C>T	NP_001334854.1:p.Gln224Ter
NM_001347926.1:c.714-965C>T	NP_001334855.1:n.714-965C>T
NM_001347927.1:c.424C>T	NP_001334856.1:p.Gln142Ter
NR_144939.1:n.3337C>T
XM_011542820.2:c.2938C>T	XP_011541122.1:p.Gln980Ter
XM_011542821.3:c.2830C>T	XP_011541123.1:p.Gln944Ter
XM_011542824.2:c.2068C>T	XP_011541126.1:p.Gln690Ter
XM_011542825.2:c.1225C>T	XP_011541127.1:p.Gln409Ter
XM_011542826.2:c.1090C>T	XP_011541128.1:p.Gln364Ter
XM_024448521.1:c.2950C>T	XP_024304289.1:p.Gln984Ter
XR_001747870.1:n.3775C>T
XR_001747872.1:n.3121C>T
XR_001747873.1:n.3435C>T
NM_001301089.2:c.844C>T	NP_001288018.1:p.Gln282Ter
NM_001347918.2:c.2584C>T	NP_001334847.2:p.Gln862Ter
NM_001347919.2:c.2574-965C>T	NP_001334848.2:n.2574-965C>T
NM_001347920.2:c.*21100C>T	NP_001334849.2:n.*21100C>T
NM_001347922.2:c.1033C>T	NP_001334851.2:p.Gln345Ter
NM_001347923.2:c.979C>T	NP_001334852.2:p.Gln327Ter
NM_001347924.2:c.724C>T	NP_001334853.1:p.Gln242Ter
NM_001347925.2:c.670C>T	NP_001334854.1:p.Gln224Ter
NM_001347926.2:c.714-965C>T	NP_001334855.1:n.714-965C>T
NM_001347927.2:c.424C>T	NP_001334856.1:p.Gln142Ter
NM_014758.3:c.2704C>T MANE Select	NP_055573.3:p.Gln902Ter
NR_144939.2:n.3329C>T