Canonical Allele Identifier: CA477582298

Gene: SNX19

Linked Data

• gnomAD v4: 11-130880707-A-T
• MyVariant Identifiers: chr11:g.130750602A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880707A>T , CM000673.2:g.130880707A>T	GRCh38
NC_000011.9:g.130750602A>T , CM000673.1:g.130750602A>T	GRCh37
NC_000011.8:g.130255812A>T	NCBI36
NG_053190.1:g.40782T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2673T>A MANE Select	ENSP00000265909.4:p.Pro891=
ENST00000265909.8:c.2673T>A	ENSP00000265909.4:p.Pro891=
ENST00000426933.6:c.177T>A	ENSP00000413345.2:p.Pro59=
ENST00000526579.5:n.178-996T>A
ENST00000527116.5:n.435T>A
ENST00000528555.5:c.813T>A	ENSP00000435122.1:p.Pro271=
ENST00000530330.1:n.409T>A
ENST00000530356.5:c.813T>A	ENSP00000432307.1:p.Pro271=
ENST00000533318.5:n.1033T>A
ENST00000534726.5:c.393T>A	ENSP00000433699.1:p.Pro131=
NM_001301089.1:c.813T>A	NP_001288018.1:p.Pro271=
NM_014758.2:c.2673T>A	NP_055573.2:p.Pro891=
XM_005271546.3:c.2574-996T>A	XP_005271603.1:n.2574-996T>A
XM_011542819.1:c.2919T>A	XP_011541121.1:p.Pro973=
XM_011542820.1:c.2907T>A	XP_011541122.1:p.Pro969=
XM_011542821.1:c.2799T>A	XP_011541123.1:p.Pro933=
XM_011542824.1:c.2037T>A	XP_011541126.1:p.Pro679=
XM_011542825.1:c.1194T>A	XP_011541127.1:p.Pro398=
XM_011542826.1:c.1059T>A	XP_011541128.1:p.Pro353=
XM_011542827.1:c.939T>A	XP_011541129.1:p.Pro313=
NM_001347918.1:c.2553T>A	NP_001334847.1:p.Pro851=
NM_001347919.1:c.2574-996T>A	NP_001334848.1:n.2574-996T>A
NM_001347922.1:c.1002T>A	NP_001334851.1:p.Pro334=
NM_001347923.1:c.948T>A	NP_001334852.1:p.Pro316=
NM_001347924.1:c.693T>A	NP_001334853.1:p.Pro231=
NM_001347925.1:c.639T>A	NP_001334854.1:p.Pro213=
NM_001347926.1:c.714-996T>A	NP_001334855.1:n.714-996T>A
NM_001347927.1:c.393T>A	NP_001334856.1:p.Pro131=
NR_144939.1:n.3306T>A
XM_011542820.2:c.2907T>A	XP_011541122.1:p.Pro969=
XM_011542821.3:c.2799T>A	XP_011541123.1:p.Pro933=
XM_011542824.2:c.2037T>A	XP_011541126.1:p.Pro679=
XM_011542825.2:c.1194T>A	XP_011541127.1:p.Pro398=
XM_011542826.2:c.1059T>A	XP_011541128.1:p.Pro353=
XM_024448521.1:c.2919T>A	XP_024304289.1:p.Pro973=
XR_001747870.1:n.3744T>A
XR_001747872.1:n.3090T>A
XR_001747873.1:n.3404T>A
NM_001301089.2:c.813T>A	NP_001288018.1:p.Pro271=
NM_001347918.2:c.2553T>A	NP_001334847.2:p.Pro851=
NM_001347919.2:c.2574-996T>A	NP_001334848.2:n.2574-996T>A
NM_001347920.2:c.*21069T>A	NP_001334849.2:n.*21069T>A
NM_001347922.2:c.1002T>A	NP_001334851.2:p.Pro334=
NM_001347923.2:c.948T>A	NP_001334852.2:p.Pro316=
NM_001347924.2:c.693T>A	NP_001334853.1:p.Pro231=
NM_001347925.2:c.639T>A	NP_001334854.1:p.Pro213=
NM_001347926.2:c.714-996T>A	NP_001334855.1:n.714-996T>A
NM_001347927.2:c.393T>A	NP_001334856.1:p.Pro131=
NM_014758.3:c.2673T>A MANE Select	NP_055573.3:p.Pro891=
NR_144939.2:n.3298T>A