Canonical Allele Identifier: CA477582340

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750668A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880773A>G , CM000673.2:g.130880773A>G	GRCh38
NC_000011.9:g.130750668A>G , CM000673.1:g.130750668A>G	GRCh37
NC_000011.8:g.130255878A>G	NCBI36
NG_053190.1:g.40716T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2607T>C MANE Select	ENSP00000265909.4:p.Ser869=
ENST00000265909.8:c.2607T>C	ENSP00000265909.4:p.Ser869=
ENST00000426933.6:c.111T>C	ENSP00000413345.2:p.Ser37=
ENST00000526579.5:n.178-1062T>C
ENST00000527116.5:n.369T>C
ENST00000528555.5:c.747T>C	ENSP00000435122.1:p.Ser249=
ENST00000530330.1:n.343T>C
ENST00000530356.5:c.747T>C	ENSP00000432307.1:p.Ser249=
ENST00000533318.5:n.967T>C
ENST00000534726.5:c.327T>C	ENSP00000433699.1:p.Ser109=
NM_001301089.1:c.747T>C	NP_001288018.1:p.Ser249=
NM_014758.2:c.2607T>C	NP_055573.2:p.Ser869=
XM_005271546.3:c.2574-1062T>C	XP_005271603.1:n.2574-1062T>C
XM_011542819.1:c.2853T>C	XP_011541121.1:p.Ser951=
XM_011542820.1:c.2841T>C	XP_011541122.1:p.Ser947=
XM_011542821.1:c.2733T>C	XP_011541123.1:p.Ser911=
XM_011542824.1:c.1971T>C	XP_011541126.1:p.Ser657=
XM_011542825.1:c.1128T>C	XP_011541127.1:p.Ser376=
XM_011542826.1:c.993T>C	XP_011541128.1:p.Ser331=
XM_011542827.1:c.873T>C	XP_011541129.1:p.Ser291=
NM_001347918.1:c.2487T>C	NP_001334847.1:p.Ser829=
NM_001347919.1:c.2574-1062T>C	NP_001334848.1:n.2574-1062T>C
NM_001347922.1:c.936T>C	NP_001334851.1:p.Ser312=
NM_001347923.1:c.882T>C	NP_001334852.1:p.Ser294=
NM_001347924.1:c.627T>C	NP_001334853.1:p.Ser209=
NM_001347925.1:c.573T>C	NP_001334854.1:p.Ser191=
NM_001347926.1:c.714-1062T>C	NP_001334855.1:n.714-1062T>C
NM_001347927.1:c.327T>C	NP_001334856.1:p.Ser109=
NR_144939.1:n.3240T>C
XM_011542820.2:c.2841T>C	XP_011541122.1:p.Ser947=
XM_011542821.3:c.2733T>C	XP_011541123.1:p.Ser911=
XM_011542824.2:c.1971T>C	XP_011541126.1:p.Ser657=
XM_011542825.2:c.1128T>C	XP_011541127.1:p.Ser376=
XM_011542826.2:c.993T>C	XP_011541128.1:p.Ser331=
XM_024448521.1:c.2853T>C	XP_024304289.1:p.Ser951=
XR_001747870.1:n.3678T>C
XR_001747872.1:n.3024T>C
XR_001747873.1:n.3338T>C
NM_001301089.2:c.747T>C	NP_001288018.1:p.Ser249=
NM_001347918.2:c.2487T>C	NP_001334847.2:p.Ser829=
NM_001347919.2:c.2574-1062T>C	NP_001334848.2:n.2574-1062T>C
NM_001347920.2:c.*21003T>C	NP_001334849.2:n.*21003T>C
NM_001347922.2:c.936T>C	NP_001334851.2:p.Ser312=
NM_001347923.2:c.882T>C	NP_001334852.2:p.Ser294=
NM_001347924.2:c.627T>C	NP_001334853.1:p.Ser209=
NM_001347925.2:c.573T>C	NP_001334854.1:p.Ser191=
NM_001347926.2:c.714-1062T>C	NP_001334855.1:n.714-1062T>C
NM_001347927.2:c.327T>C	NP_001334856.1:p.Ser109=
NM_014758.3:c.2607T>C MANE Select	NP_055573.3:p.Ser869=
NR_144939.2:n.3232T>C