Canonical Allele Identifier: CA477582287

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750590C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880695C>A , CM000673.2:g.130880695C>A	GRCh38
NC_000011.9:g.130750590C>A , CM000673.1:g.130750590C>A	GRCh37
NC_000011.8:g.130255800C>A	NCBI36
NG_053190.1:g.40794G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2685G>T MANE Select	ENSP00000265909.4:p.Arg895=
ENST00000265909.8:c.2685G>T	ENSP00000265909.4:p.Arg895=
ENST00000426933.6:c.189G>T	ENSP00000413345.2:p.Arg63=
ENST00000526579.5:n.178-984G>T
ENST00000527116.5:n.447G>T
ENST00000528555.5:c.825G>T	ENSP00000435122.1:p.Arg275=
ENST00000530330.1:n.421G>T
ENST00000530356.5:c.825G>T	ENSP00000432307.1:p.Arg275=
ENST00000533318.5:n.1045G>T
ENST00000534726.5:c.405G>T	ENSP00000433699.1:p.Arg135=
NM_001301089.1:c.825G>T	NP_001288018.1:p.Arg275=
NM_014758.2:c.2685G>T	NP_055573.2:p.Arg895=
XM_005271546.3:c.2574-984G>T	XP_005271603.1:n.2574-984G>T
XM_011542819.1:c.2931G>T	XP_011541121.1:p.Arg977=
XM_011542820.1:c.2919G>T	XP_011541122.1:p.Arg973=
XM_011542821.1:c.2811G>T	XP_011541123.1:p.Arg937=
XM_011542824.1:c.2049G>T	XP_011541126.1:p.Arg683=
XM_011542825.1:c.1206G>T	XP_011541127.1:p.Arg402=
XM_011542826.1:c.1071G>T	XP_011541128.1:p.Arg357=
XM_011542827.1:c.951G>T	XP_011541129.1:p.Arg317=
NM_001347918.1:c.2565G>T	NP_001334847.1:p.Arg855=
NM_001347919.1:c.2574-984G>T	NP_001334848.1:n.2574-984G>T
NM_001347922.1:c.1014G>T	NP_001334851.1:p.Arg338=
NM_001347923.1:c.960G>T	NP_001334852.1:p.Arg320=
NM_001347924.1:c.705G>T	NP_001334853.1:p.Arg235=
NM_001347925.1:c.651G>T	NP_001334854.1:p.Arg217=
NM_001347926.1:c.714-984G>T	NP_001334855.1:n.714-984G>T
NM_001347927.1:c.405G>T	NP_001334856.1:p.Arg135=
NR_144939.1:n.3318G>T
XM_011542820.2:c.2919G>T	XP_011541122.1:p.Arg973=
XM_011542821.3:c.2811G>T	XP_011541123.1:p.Arg937=
XM_011542824.2:c.2049G>T	XP_011541126.1:p.Arg683=
XM_011542825.2:c.1206G>T	XP_011541127.1:p.Arg402=
XM_011542826.2:c.1071G>T	XP_011541128.1:p.Arg357=
XM_024448521.1:c.2931G>T	XP_024304289.1:p.Arg977=
XR_001747870.1:n.3756G>T
XR_001747872.1:n.3102G>T
XR_001747873.1:n.3416G>T
NM_001301089.2:c.825G>T	NP_001288018.1:p.Arg275=
NM_001347918.2:c.2565G>T	NP_001334847.2:p.Arg855=
NM_001347919.2:c.2574-984G>T	NP_001334848.2:n.2574-984G>T
NM_001347920.2:c.*21081G>T	NP_001334849.2:n.*21081G>T
NM_001347922.2:c.1014G>T	NP_001334851.2:p.Arg338=
NM_001347923.2:c.960G>T	NP_001334852.2:p.Arg320=
NM_001347924.2:c.705G>T	NP_001334853.1:p.Arg235=
NM_001347925.2:c.651G>T	NP_001334854.1:p.Arg217=
NM_001347926.2:c.714-984G>T	NP_001334855.1:n.714-984G>T
NM_001347927.2:c.405G>T	NP_001334856.1:p.Arg135=
NM_014758.3:c.2685G>T MANE Select	NP_055573.3:p.Arg895=
NR_144939.2:n.3310G>T