Canonical Allele Identifier: CA383457631

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750543A>C (hg19) ; chr11:g.130880648A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880648A>C , CM000673.2:g.130880648A>C	GRCh38
NC_000011.9:g.130750543A>C , CM000673.1:g.130750543A>C	GRCh37
NC_000011.8:g.130255753A>C	NCBI36
NG_053190.1:g.40841T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2732T>G MANE Select	ENSP00000265909.4:p.Leu911Trp
ENST00000265909.8:c.2732T>G	ENSP00000265909.4:p.Leu911Trp
ENST00000426933.6:c.236T>G	ENSP00000413345.2:p.Leu79Trp
ENST00000526579.5:n.178-937T>G
ENST00000527116.5:n.494T>G
ENST00000528555.5:c.872T>G	ENSP00000435122.1:p.Leu291Trp
ENST00000530330.1:n.468T>G
ENST00000530356.5:c.872T>G	ENSP00000432307.1:p.Leu291Trp
ENST00000533318.5:n.1092T>G
ENST00000534726.5:c.452T>G	ENSP00000433699.1:p.Leu151Trp
NM_001301089.1:c.872T>G	NP_001288018.1:p.Leu291Trp
NM_014758.2:c.2732T>G	NP_055573.2:p.Leu911Trp
XM_005271546.3:c.2574-937T>G	XP_005271603.1:n.2574-937T>G
XM_011542819.1:c.2978T>G	XP_011541121.1:p.Leu993Trp
XM_011542820.1:c.2966T>G	XP_011541122.1:p.Leu989Trp
XM_011542821.1:c.2858T>G	XP_011541123.1:p.Leu953Trp
XM_011542824.1:c.2096T>G	XP_011541126.1:p.Leu699Trp
XM_011542825.1:c.1253T>G	XP_011541127.1:p.Leu418Trp
XM_011542826.1:c.1118T>G	XP_011541128.1:p.Leu373Trp
XM_011542827.1:c.998T>G	XP_011541129.1:p.Leu333Trp
NM_001347918.1:c.2612T>G	NP_001334847.1:p.Leu871Trp
NM_001347919.1:c.2574-937T>G	NP_001334848.1:n.2574-937T>G
NM_001347922.1:c.1061T>G	NP_001334851.1:p.Leu354Trp
NM_001347923.1:c.1007T>G	NP_001334852.1:p.Leu336Trp
NM_001347924.1:c.752T>G	NP_001334853.1:p.Leu251Trp
NM_001347925.1:c.698T>G	NP_001334854.1:p.Leu233Trp
NM_001347926.1:c.714-937T>G	NP_001334855.1:n.714-937T>G
NM_001347927.1:c.452T>G	NP_001334856.1:p.Leu151Trp
NR_144939.1:n.3365T>G
XM_011542820.2:c.2966T>G	XP_011541122.1:p.Leu989Trp
XM_011542821.3:c.2858T>G	XP_011541123.1:p.Leu953Trp
XM_011542824.2:c.2096T>G	XP_011541126.1:p.Leu699Trp
XM_011542825.2:c.1253T>G	XP_011541127.1:p.Leu418Trp
XM_011542826.2:c.1118T>G	XP_011541128.1:p.Leu373Trp
XM_024448521.1:c.2978T>G	XP_024304289.1:p.Leu993Trp
XR_001747870.1:n.3803T>G
XR_001747872.1:n.3149T>G
XR_001747873.1:n.3463T>G
NM_001301089.2:c.872T>G	NP_001288018.1:p.Leu291Trp
NM_001347918.2:c.2612T>G	NP_001334847.2:p.Leu871Trp
NM_001347919.2:c.2574-937T>G	NP_001334848.2:n.2574-937T>G
NM_001347920.2:c.*21128T>G	NP_001334849.2:n.*21128T>G
NM_001347922.2:c.1061T>G	NP_001334851.2:p.Leu354Trp
NM_001347923.2:c.1007T>G	NP_001334852.2:p.Leu336Trp
NM_001347924.2:c.752T>G	NP_001334853.1:p.Leu251Trp
NM_001347925.2:c.698T>G	NP_001334854.1:p.Leu233Trp
NM_001347926.2:c.714-937T>G	NP_001334855.1:n.714-937T>G
NM_001347927.2:c.452T>G	NP_001334856.1:p.Leu151Trp
NM_014758.3:c.2732T>G MANE Select	NP_055573.3:p.Leu911Trp
NR_144939.2:n.3357T>G