Canonical Allele Identifier: CA6366573

Gene: SNX19

Linked Data

• dbSNP Id: rs777612942
• ExAC: 11:130750559 C / G
• gnomAD v2: 11-130750559-C-G
• gnomAD v4: 11-130880664-C-G
• MyVariant Identifiers: chr11:g.130750559C>G (hg19) ; chr11:g.130880664C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880664C>G , CM000673.2:g.130880664C>G	GRCh38
NC_000011.9:g.130750559C>G , CM000673.1:g.130750559C>G	GRCh37
NC_000011.8:g.130255769C>G	NCBI36
NG_053190.1:g.40825G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2716G>C MANE Select	ENSP00000265909.4:p.Ala906Pro
ENST00000265909.8:c.2716G>C	ENSP00000265909.4:p.Ala906Pro
ENST00000426933.6:c.220G>C	ENSP00000413345.2:p.Ala74Pro
ENST00000526579.5:n.178-953G>C
ENST00000527116.5:n.478G>C
ENST00000528555.5:c.856G>C	ENSP00000435122.1:p.Ala286Pro
ENST00000530330.1:n.452G>C
ENST00000530356.5:c.856G>C	ENSP00000432307.1:p.Ala286Pro
ENST00000533318.5:n.1076G>C
ENST00000534726.5:c.436G>C	ENSP00000433699.1:p.Ala146Pro
NM_001301089.1:c.856G>C	NP_001288018.1:p.Ala286Pro
NM_014758.2:c.2716G>C	NP_055573.2:p.Ala906Pro
XM_005271546.3:c.2574-953G>C	XP_005271603.1:n.2574-953G>C
XM_011542819.1:c.2962G>C	XP_011541121.1:p.Ala988Pro
XM_011542820.1:c.2950G>C	XP_011541122.1:p.Ala984Pro
XM_011542821.1:c.2842G>C	XP_011541123.1:p.Ala948Pro
XM_011542824.1:c.2080G>C	XP_011541126.1:p.Ala694Pro
XM_011542825.1:c.1237G>C	XP_011541127.1:p.Ala413Pro
XM_011542826.1:c.1102G>C	XP_011541128.1:p.Ala368Pro
XM_011542827.1:c.982G>C	XP_011541129.1:p.Ala328Pro
NM_001347918.1:c.2596G>C	NP_001334847.1:p.Ala866Pro
NM_001347919.1:c.2574-953G>C	NP_001334848.1:n.2574-953G>C
NM_001347922.1:c.1045G>C	NP_001334851.1:p.Ala349Pro
NM_001347923.1:c.991G>C	NP_001334852.1:p.Ala331Pro
NM_001347924.1:c.736G>C	NP_001334853.1:p.Ala246Pro
NM_001347925.1:c.682G>C	NP_001334854.1:p.Ala228Pro
NM_001347926.1:c.714-953G>C	NP_001334855.1:n.714-953G>C
NM_001347927.1:c.436G>C	NP_001334856.1:p.Ala146Pro
NR_144939.1:n.3349G>C
XM_011542820.2:c.2950G>C	XP_011541122.1:p.Ala984Pro
XM_011542821.3:c.2842G>C	XP_011541123.1:p.Ala948Pro
XM_011542824.2:c.2080G>C	XP_011541126.1:p.Ala694Pro
XM_011542825.2:c.1237G>C	XP_011541127.1:p.Ala413Pro
XM_011542826.2:c.1102G>C	XP_011541128.1:p.Ala368Pro
XM_024448521.1:c.2962G>C	XP_024304289.1:p.Ala988Pro
XR_001747870.1:n.3787G>C
XR_001747872.1:n.3133G>C
XR_001747873.1:n.3447G>C
NM_001301089.2:c.856G>C	NP_001288018.1:p.Ala286Pro
NM_001347918.2:c.2596G>C	NP_001334847.2:p.Ala866Pro
NM_001347919.2:c.2574-953G>C	NP_001334848.2:n.2574-953G>C
NM_001347920.2:c.*21112G>C	NP_001334849.2:n.*21112G>C
NM_001347922.2:c.1045G>C	NP_001334851.2:p.Ala349Pro
NM_001347923.2:c.991G>C	NP_001334852.2:p.Ala331Pro
NM_001347924.2:c.736G>C	NP_001334853.1:p.Ala246Pro
NM_001347925.2:c.682G>C	NP_001334854.1:p.Ala228Pro
NM_001347926.2:c.714-953G>C	NP_001334855.1:n.714-953G>C
NM_001347927.2:c.436G>C	NP_001334856.1:p.Ala146Pro
NM_014758.3:c.2716G>C MANE Select	NP_055573.3:p.Ala906Pro
NR_144939.2:n.3341G>C