Canonical Allele Identifier: CA477582313

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750623G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880728G>A , CM000673.2:g.130880728G>A	GRCh38
NC_000011.9:g.130750623G>A , CM000673.1:g.130750623G>A	GRCh37
NC_000011.8:g.130255833G>A	NCBI36
NG_053190.1:g.40761C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2652C>T MANE Select	ENSP00000265909.4:p.Ile884=
ENST00000265909.8:c.2652C>T	ENSP00000265909.4:p.Ile884=
ENST00000426933.6:c.156C>T	ENSP00000413345.2:p.Ile52=
ENST00000526579.5:n.178-1017C>T
ENST00000527116.5:n.414C>T
ENST00000528555.5:c.792C>T	ENSP00000435122.1:p.Ile264=
ENST00000530330.1:n.388C>T
ENST00000530356.5:c.792C>T	ENSP00000432307.1:p.Ile264=
ENST00000533318.5:n.1012C>T
ENST00000534726.5:c.372C>T	ENSP00000433699.1:p.Ile124=
NM_001301089.1:c.792C>T	NP_001288018.1:p.Ile264=
NM_014758.2:c.2652C>T	NP_055573.2:p.Ile884=
XM_005271546.3:c.2574-1017C>T	XP_005271603.1:n.2574-1017C>T
XM_011542819.1:c.2898C>T	XP_011541121.1:p.Ile966=
XM_011542820.1:c.2886C>T	XP_011541122.1:p.Ile962=
XM_011542821.1:c.2778C>T	XP_011541123.1:p.Ile926=
XM_011542824.1:c.2016C>T	XP_011541126.1:p.Ile672=
XM_011542825.1:c.1173C>T	XP_011541127.1:p.Ile391=
XM_011542826.1:c.1038C>T	XP_011541128.1:p.Ile346=
XM_011542827.1:c.918C>T	XP_011541129.1:p.Ile306=
NM_001347918.1:c.2532C>T	NP_001334847.1:p.Ile844=
NM_001347919.1:c.2574-1017C>T	NP_001334848.1:n.2574-1017C>T
NM_001347922.1:c.981C>T	NP_001334851.1:p.Ile327=
NM_001347923.1:c.927C>T	NP_001334852.1:p.Ile309=
NM_001347924.1:c.672C>T	NP_001334853.1:p.Ile224=
NM_001347925.1:c.618C>T	NP_001334854.1:p.Ile206=
NM_001347926.1:c.714-1017C>T	NP_001334855.1:n.714-1017C>T
NM_001347927.1:c.372C>T	NP_001334856.1:p.Ile124=
NR_144939.1:n.3285C>T
XM_011542820.2:c.2886C>T	XP_011541122.1:p.Ile962=
XM_011542821.3:c.2778C>T	XP_011541123.1:p.Ile926=
XM_011542824.2:c.2016C>T	XP_011541126.1:p.Ile672=
XM_011542825.2:c.1173C>T	XP_011541127.1:p.Ile391=
XM_011542826.2:c.1038C>T	XP_011541128.1:p.Ile346=
XM_024448521.1:c.2898C>T	XP_024304289.1:p.Ile966=
XR_001747870.1:n.3723C>T
XR_001747872.1:n.3069C>T
XR_001747873.1:n.3383C>T
NM_001301089.2:c.792C>T	NP_001288018.1:p.Ile264=
NM_001347918.2:c.2532C>T	NP_001334847.2:p.Ile844=
NM_001347919.2:c.2574-1017C>T	NP_001334848.2:n.2574-1017C>T
NM_001347920.2:c.*21048C>T	NP_001334849.2:n.*21048C>T
NM_001347922.2:c.981C>T	NP_001334851.2:p.Ile327=
NM_001347923.2:c.927C>T	NP_001334852.2:p.Ile309=
NM_001347924.2:c.672C>T	NP_001334853.1:p.Ile224=
NM_001347925.2:c.618C>T	NP_001334854.1:p.Ile206=
NM_001347926.2:c.714-1017C>T	NP_001334855.1:n.714-1017C>T
NM_001347927.2:c.372C>T	NP_001334856.1:p.Ile124=
NM_014758.3:c.2652C>T MANE Select	NP_055573.3:p.Ile884=
NR_144939.2:n.3277C>T