Canonical Allele Identifier: CA477582325

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750641C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880746C>A , CM000673.2:g.130880746C>A	GRCh38
NC_000011.9:g.130750641C>A , CM000673.1:g.130750641C>A	GRCh37
NC_000011.8:g.130255851C>A	NCBI36
NG_053190.1:g.40743G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2634G>T MANE Select	ENSP00000265909.4:p.Leu878=
ENST00000265909.8:c.2634G>T	ENSP00000265909.4:p.Leu878=
ENST00000426933.6:c.138G>T	ENSP00000413345.2:p.Leu46=
ENST00000526579.5:n.178-1035G>T
ENST00000527116.5:n.396G>T
ENST00000528555.5:c.774G>T	ENSP00000435122.1:p.Leu258=
ENST00000530330.1:n.370G>T
ENST00000530356.5:c.774G>T	ENSP00000432307.1:p.Leu258=
ENST00000533318.5:n.994G>T
ENST00000534726.5:c.354G>T	ENSP00000433699.1:p.Leu118=
NM_001301089.1:c.774G>T	NP_001288018.1:p.Leu258=
NM_014758.2:c.2634G>T	NP_055573.2:p.Leu878=
XM_005271546.3:c.2574-1035G>T	XP_005271603.1:n.2574-1035G>T
XM_011542819.1:c.2880G>T	XP_011541121.1:p.Leu960=
XM_011542820.1:c.2868G>T	XP_011541122.1:p.Leu956=
XM_011542821.1:c.2760G>T	XP_011541123.1:p.Leu920=
XM_011542824.1:c.1998G>T	XP_011541126.1:p.Leu666=
XM_011542825.1:c.1155G>T	XP_011541127.1:p.Leu385=
XM_011542826.1:c.1020G>T	XP_011541128.1:p.Leu340=
XM_011542827.1:c.900G>T	XP_011541129.1:p.Leu300=
NM_001347918.1:c.2514G>T	NP_001334847.1:p.Leu838=
NM_001347919.1:c.2574-1035G>T	NP_001334848.1:n.2574-1035G>T
NM_001347922.1:c.963G>T	NP_001334851.1:p.Leu321=
NM_001347923.1:c.909G>T	NP_001334852.1:p.Leu303=
NM_001347924.1:c.654G>T	NP_001334853.1:p.Leu218=
NM_001347925.1:c.600G>T	NP_001334854.1:p.Leu200=
NM_001347926.1:c.714-1035G>T	NP_001334855.1:n.714-1035G>T
NM_001347927.1:c.354G>T	NP_001334856.1:p.Leu118=
NR_144939.1:n.3267G>T
XM_011542820.2:c.2868G>T	XP_011541122.1:p.Leu956=
XM_011542821.3:c.2760G>T	XP_011541123.1:p.Leu920=
XM_011542824.2:c.1998G>T	XP_011541126.1:p.Leu666=
XM_011542825.2:c.1155G>T	XP_011541127.1:p.Leu385=
XM_011542826.2:c.1020G>T	XP_011541128.1:p.Leu340=
XM_024448521.1:c.2880G>T	XP_024304289.1:p.Leu960=
XR_001747870.1:n.3705G>T
XR_001747872.1:n.3051G>T
XR_001747873.1:n.3365G>T
NM_001301089.2:c.774G>T	NP_001288018.1:p.Leu258=
NM_001347918.2:c.2514G>T	NP_001334847.2:p.Leu838=
NM_001347919.2:c.2574-1035G>T	NP_001334848.2:n.2574-1035G>T
NM_001347920.2:c.*21030G>T	NP_001334849.2:n.*21030G>T
NM_001347922.2:c.963G>T	NP_001334851.2:p.Leu321=
NM_001347923.2:c.909G>T	NP_001334852.2:p.Leu303=
NM_001347924.2:c.654G>T	NP_001334853.1:p.Leu218=
NM_001347925.2:c.600G>T	NP_001334854.1:p.Leu200=
NM_001347926.2:c.714-1035G>T	NP_001334855.1:n.714-1035G>T
NM_001347927.2:c.354G>T	NP_001334856.1:p.Leu118=
NM_014758.3:c.2634G>T MANE Select	NP_055573.3:p.Leu878=
NR_144939.2:n.3259G>T