Canonical Allele Identifier: CA477582273

Gene: SNX19

Linked Data

• gnomAD v4: 11-130880674-C-T
• MyVariant Identifiers: chr11:g.130750569C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880674C>T , CM000673.2:g.130880674C>T	GRCh38
NC_000011.9:g.130750569C>T , CM000673.1:g.130750569C>T	GRCh37
NC_000011.8:g.130255779C>T	NCBI36
NG_053190.1:g.40815G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2706G>A MANE Select	ENSP00000265909.4:p.Gln902=
ENST00000265909.8:c.2706G>A	ENSP00000265909.4:p.Gln902=
ENST00000426933.6:c.210G>A	ENSP00000413345.2:p.Gln70=
ENST00000526579.5:n.178-963G>A
ENST00000527116.5:n.468G>A
ENST00000528555.5:c.846G>A	ENSP00000435122.1:p.Gln282=
ENST00000530330.1:n.442G>A
ENST00000530356.5:c.846G>A	ENSP00000432307.1:p.Gln282=
ENST00000533318.5:n.1066G>A
ENST00000534726.5:c.426G>A	ENSP00000433699.1:p.Gln142=
NM_001301089.1:c.846G>A	NP_001288018.1:p.Gln282=
NM_014758.2:c.2706G>A	NP_055573.2:p.Gln902=
XM_005271546.3:c.2574-963G>A	XP_005271603.1:n.2574-963G>A
XM_011542819.1:c.2952G>A	XP_011541121.1:p.Gln984=
XM_011542820.1:c.2940G>A	XP_011541122.1:p.Gln980=
XM_011542821.1:c.2832G>A	XP_011541123.1:p.Gln944=
XM_011542824.1:c.2070G>A	XP_011541126.1:p.Gln690=
XM_011542825.1:c.1227G>A	XP_011541127.1:p.Gln409=
XM_011542826.1:c.1092G>A	XP_011541128.1:p.Gln364=
XM_011542827.1:c.972G>A	XP_011541129.1:p.Gln324=
NM_001347918.1:c.2586G>A	NP_001334847.1:p.Gln862=
NM_001347919.1:c.2574-963G>A	NP_001334848.1:n.2574-963G>A
NM_001347922.1:c.1035G>A	NP_001334851.1:p.Gln345=
NM_001347923.1:c.981G>A	NP_001334852.1:p.Gln327=
NM_001347924.1:c.726G>A	NP_001334853.1:p.Gln242=
NM_001347925.1:c.672G>A	NP_001334854.1:p.Gln224=
NM_001347926.1:c.714-963G>A	NP_001334855.1:n.714-963G>A
NM_001347927.1:c.426G>A	NP_001334856.1:p.Gln142=
NR_144939.1:n.3339G>A
XM_011542820.2:c.2940G>A	XP_011541122.1:p.Gln980=
XM_011542821.3:c.2832G>A	XP_011541123.1:p.Gln944=
XM_011542824.2:c.2070G>A	XP_011541126.1:p.Gln690=
XM_011542825.2:c.1227G>A	XP_011541127.1:p.Gln409=
XM_011542826.2:c.1092G>A	XP_011541128.1:p.Gln364=
XM_024448521.1:c.2952G>A	XP_024304289.1:p.Gln984=
XR_001747870.1:n.3777G>A
XR_001747872.1:n.3123G>A
XR_001747873.1:n.3437G>A
NM_001301089.2:c.846G>A	NP_001288018.1:p.Gln282=
NM_001347918.2:c.2586G>A	NP_001334847.2:p.Gln862=
NM_001347919.2:c.2574-963G>A	NP_001334848.2:n.2574-963G>A
NM_001347920.2:c.*21102G>A	NP_001334849.2:n.*21102G>A
NM_001347922.2:c.1035G>A	NP_001334851.2:p.Gln345=
NM_001347923.2:c.981G>A	NP_001334852.2:p.Gln327=
NM_001347924.2:c.726G>A	NP_001334853.1:p.Gln242=
NM_001347925.2:c.672G>A	NP_001334854.1:p.Gln224=
NM_001347926.2:c.714-963G>A	NP_001334855.1:n.714-963G>A
NM_001347927.2:c.426G>A	NP_001334856.1:p.Gln142=
NM_014758.3:c.2706G>A MANE Select	NP_055573.3:p.Gln902=
NR_144939.2:n.3331G>A