Canonical Allele Identifier: CA6366583

Gene: SNX19

Linked Data

• dbSNP Id: rs773483188
• ExAC: 11:130750625 T / G
• gnomAD v2: 11-130750625-T-G
• gnomAD v4: 11-130880730-T-G
• MyVariant Identifiers: chr11:g.130750625T>G (hg19) ; chr11:g.130880730T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880730T>G , CM000673.2:g.130880730T>G	GRCh38
NC_000011.9:g.130750625T>G , CM000673.1:g.130750625T>G	GRCh37
NC_000011.8:g.130255835T>G	NCBI36
NG_053190.1:g.40759A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2650A>C MANE Select	ENSP00000265909.4:p.Ile884Leu
ENST00000265909.8:c.2650A>C	ENSP00000265909.4:p.Ile884Leu
ENST00000426933.6:c.154A>C	ENSP00000413345.2:p.Ile52Leu
ENST00000526579.5:n.178-1019A>C
ENST00000527116.5:n.412A>C
ENST00000528555.5:c.790A>C	ENSP00000435122.1:p.Ile264Leu
ENST00000530330.1:n.386A>C
ENST00000530356.5:c.790A>C	ENSP00000432307.1:p.Ile264Leu
ENST00000533318.5:n.1010A>C
ENST00000534726.5:c.370A>C	ENSP00000433699.1:p.Ile124Leu
NM_001301089.1:c.790A>C	NP_001288018.1:p.Ile264Leu
NM_014758.2:c.2650A>C	NP_055573.2:p.Ile884Leu
XM_005271546.3:c.2574-1019A>C	XP_005271603.1:n.2574-1019A>C
XM_011542819.1:c.2896A>C	XP_011541121.1:p.Ile966Leu
XM_011542820.1:c.2884A>C	XP_011541122.1:p.Ile962Leu
XM_011542821.1:c.2776A>C	XP_011541123.1:p.Ile926Leu
XM_011542824.1:c.2014A>C	XP_011541126.1:p.Ile672Leu
XM_011542825.1:c.1171A>C	XP_011541127.1:p.Ile391Leu
XM_011542826.1:c.1036A>C	XP_011541128.1:p.Ile346Leu
XM_011542827.1:c.916A>C	XP_011541129.1:p.Ile306Leu
NM_001347918.1:c.2530A>C	NP_001334847.1:p.Ile844Leu
NM_001347919.1:c.2574-1019A>C	NP_001334848.1:n.2574-1019A>C
NM_001347922.1:c.979A>C	NP_001334851.1:p.Ile327Leu
NM_001347923.1:c.925A>C	NP_001334852.1:p.Ile309Leu
NM_001347924.1:c.670A>C	NP_001334853.1:p.Ile224Leu
NM_001347925.1:c.616A>C	NP_001334854.1:p.Ile206Leu
NM_001347926.1:c.714-1019A>C	NP_001334855.1:n.714-1019A>C
NM_001347927.1:c.370A>C	NP_001334856.1:p.Ile124Leu
NR_144939.1:n.3283A>C
XM_011542820.2:c.2884A>C	XP_011541122.1:p.Ile962Leu
XM_011542821.3:c.2776A>C	XP_011541123.1:p.Ile926Leu
XM_011542824.2:c.2014A>C	XP_011541126.1:p.Ile672Leu
XM_011542825.2:c.1171A>C	XP_011541127.1:p.Ile391Leu
XM_011542826.2:c.1036A>C	XP_011541128.1:p.Ile346Leu
XM_024448521.1:c.2896A>C	XP_024304289.1:p.Ile966Leu
XR_001747870.1:n.3721A>C
XR_001747872.1:n.3067A>C
XR_001747873.1:n.3381A>C
NM_001301089.2:c.790A>C	NP_001288018.1:p.Ile264Leu
NM_001347918.2:c.2530A>C	NP_001334847.2:p.Ile844Leu
NM_001347919.2:c.2574-1019A>C	NP_001334848.2:n.2574-1019A>C
NM_001347920.2:c.*21046A>C	NP_001334849.2:n.*21046A>C
NM_001347922.2:c.979A>C	NP_001334851.2:p.Ile327Leu
NM_001347923.2:c.925A>C	NP_001334852.2:p.Ile309Leu
NM_001347924.2:c.670A>C	NP_001334853.1:p.Ile224Leu
NM_001347925.2:c.616A>C	NP_001334854.1:p.Ile206Leu
NM_001347926.2:c.714-1019A>C	NP_001334855.1:n.714-1019A>C
NM_001347927.2:c.370A>C	NP_001334856.1:p.Ile124Leu
NM_014758.3:c.2650A>C MANE Select	NP_055573.3:p.Ile884Leu
NR_144939.2:n.3275A>C