Canonical Allele Identifier: CA383457665

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750558G>T (hg19) ; chr11:g.130880663G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880663G>T , CM000673.2:g.130880663G>T	GRCh38
NC_000011.9:g.130750558G>T , CM000673.1:g.130750558G>T	GRCh37
NC_000011.8:g.130255768G>T	NCBI36
NG_053190.1:g.40826C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2717C>A MANE Select	ENSP00000265909.4:p.Ala906Asp
ENST00000265909.8:c.2717C>A	ENSP00000265909.4:p.Ala906Asp
ENST00000426933.6:c.221C>A	ENSP00000413345.2:p.Ala74Asp
ENST00000526579.5:n.178-952C>A
ENST00000527116.5:n.479C>A
ENST00000528555.5:c.857C>A	ENSP00000435122.1:p.Ala286Asp
ENST00000530330.1:n.453C>A
ENST00000530356.5:c.857C>A	ENSP00000432307.1:p.Ala286Asp
ENST00000533318.5:n.1077C>A
ENST00000534726.5:c.437C>A	ENSP00000433699.1:p.Ala146Asp
NM_001301089.1:c.857C>A	NP_001288018.1:p.Ala286Asp
NM_014758.2:c.2717C>A	NP_055573.2:p.Ala906Asp
XM_005271546.3:c.2574-952C>A	XP_005271603.1:n.2574-952C>A
XM_011542819.1:c.2963C>A	XP_011541121.1:p.Ala988Asp
XM_011542820.1:c.2951C>A	XP_011541122.1:p.Ala984Asp
XM_011542821.1:c.2843C>A	XP_011541123.1:p.Ala948Asp
XM_011542824.1:c.2081C>A	XP_011541126.1:p.Ala694Asp
XM_011542825.1:c.1238C>A	XP_011541127.1:p.Ala413Asp
XM_011542826.1:c.1103C>A	XP_011541128.1:p.Ala368Asp
XM_011542827.1:c.983C>A	XP_011541129.1:p.Ala328Asp
NM_001347918.1:c.2597C>A	NP_001334847.1:p.Ala866Asp
NM_001347919.1:c.2574-952C>A	NP_001334848.1:n.2574-952C>A
NM_001347922.1:c.1046C>A	NP_001334851.1:p.Ala349Asp
NM_001347923.1:c.992C>A	NP_001334852.1:p.Ala331Asp
NM_001347924.1:c.737C>A	NP_001334853.1:p.Ala246Asp
NM_001347925.1:c.683C>A	NP_001334854.1:p.Ala228Asp
NM_001347926.1:c.714-952C>A	NP_001334855.1:n.714-952C>A
NM_001347927.1:c.437C>A	NP_001334856.1:p.Ala146Asp
NR_144939.1:n.3350C>A
XM_011542820.2:c.2951C>A	XP_011541122.1:p.Ala984Asp
XM_011542821.3:c.2843C>A	XP_011541123.1:p.Ala948Asp
XM_011542824.2:c.2081C>A	XP_011541126.1:p.Ala694Asp
XM_011542825.2:c.1238C>A	XP_011541127.1:p.Ala413Asp
XM_011542826.2:c.1103C>A	XP_011541128.1:p.Ala368Asp
XM_024448521.1:c.2963C>A	XP_024304289.1:p.Ala988Asp
XR_001747870.1:n.3788C>A
XR_001747872.1:n.3134C>A
XR_001747873.1:n.3448C>A
NM_001301089.2:c.857C>A	NP_001288018.1:p.Ala286Asp
NM_001347918.2:c.2597C>A	NP_001334847.2:p.Ala866Asp
NM_001347919.2:c.2574-952C>A	NP_001334848.2:n.2574-952C>A
NM_001347920.2:c.*21113C>A	NP_001334849.2:n.*21113C>A
NM_001347922.2:c.1046C>A	NP_001334851.2:p.Ala349Asp
NM_001347923.2:c.992C>A	NP_001334852.2:p.Ala331Asp
NM_001347924.2:c.737C>A	NP_001334853.1:p.Ala246Asp
NM_001347925.2:c.683C>A	NP_001334854.1:p.Ala228Asp
NM_001347926.2:c.714-952C>A	NP_001334855.1:n.714-952C>A
NM_001347927.2:c.437C>A	NP_001334856.1:p.Ala146Asp
NM_014758.3:c.2717C>A MANE Select	NP_055573.3:p.Ala906Asp
NR_144939.2:n.3342C>A