Canonical Allele Identifier: CA383457630

Gene: SNX19

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2732T>C MANE Select	ENSP00000265909.4:p.Leu911Ser
ENST00000265909.8:c.2732T>C	ENSP00000265909.4:p.Leu911Ser
ENST00000426933.6:c.236T>C	ENSP00000413345.2:p.Leu79Ser
ENST00000526579.5:n.178-937T>C
ENST00000527116.5:n.494T>C
ENST00000528555.5:c.872T>C	ENSP00000435122.1:p.Leu291Ser
ENST00000530330.1:n.468T>C
ENST00000530356.5:c.872T>C	ENSP00000432307.1:p.Leu291Ser
ENST00000533318.5:n.1092T>C
ENST00000534726.5:c.452T>C	ENSP00000433699.1:p.Leu151Ser
NM_001301089.1:c.872T>C	NP_001288018.1:p.Leu291Ser
NM_014758.2:c.2732T>C	NP_055573.2:p.Leu911Ser
XM_005271546.3:c.2574-937T>C	XP_005271603.1:n.2574-937T>C
XM_011542819.1:c.2978T>C	XP_011541121.1:p.Leu993Ser
XM_011542820.1:c.2966T>C	XP_011541122.1:p.Leu989Ser
XM_011542821.1:c.2858T>C	XP_011541123.1:p.Leu953Ser
XM_011542824.1:c.2096T>C	XP_011541126.1:p.Leu699Ser
XM_011542825.1:c.1253T>C	XP_011541127.1:p.Leu418Ser
XM_011542826.1:c.1118T>C	XP_011541128.1:p.Leu373Ser
XM_011542827.1:c.998T>C	XP_011541129.1:p.Leu333Ser
NM_001347918.1:c.2612T>C	NP_001334847.1:p.Leu871Ser
NM_001347919.1:c.2574-937T>C	NP_001334848.1:n.2574-937T>C
NM_001347922.1:c.1061T>C	NP_001334851.1:p.Leu354Ser
NM_001347923.1:c.1007T>C	NP_001334852.1:p.Leu336Ser
NM_001347924.1:c.752T>C	NP_001334853.1:p.Leu251Ser
NM_001347925.1:c.698T>C	NP_001334854.1:p.Leu233Ser
NM_001347926.1:c.714-937T>C	NP_001334855.1:n.714-937T>C
NM_001347927.1:c.452T>C	NP_001334856.1:p.Leu151Ser
NR_144939.1:n.3365T>C
XM_011542820.2:c.2966T>C	XP_011541122.1:p.Leu989Ser
XM_011542821.3:c.2858T>C	XP_011541123.1:p.Leu953Ser
XM_011542824.2:c.2096T>C	XP_011541126.1:p.Leu699Ser
XM_011542825.2:c.1253T>C	XP_011541127.1:p.Leu418Ser
XM_011542826.2:c.1118T>C	XP_011541128.1:p.Leu373Ser
XM_024448521.1:c.2978T>C	XP_024304289.1:p.Leu993Ser
XR_001747870.1:n.3803T>C
XR_001747872.1:n.3149T>C
XR_001747873.1:n.3463T>C
NM_001301089.2:c.872T>C	NP_001288018.1:p.Leu291Ser
NM_001347918.2:c.2612T>C	NP_001334847.2:p.Leu871Ser
NM_001347919.2:c.2574-937T>C	NP_001334848.2:n.2574-937T>C
NM_001347920.2:c.*21128T>C	NP_001334849.2:n.*21128T>C
NM_001347922.2:c.1061T>C	NP_001334851.2:p.Leu354Ser
NM_001347923.2:c.1007T>C	NP_001334852.2:p.Leu336Ser
NM_001347924.2:c.752T>C	NP_001334853.1:p.Leu251Ser
NM_001347925.2:c.698T>C	NP_001334854.1:p.Leu233Ser
NM_001347926.2:c.714-937T>C	NP_001334855.1:n.714-937T>C
NM_001347927.2:c.452T>C	NP_001334856.1:p.Leu151Ser
NM_014758.3:c.2732T>C MANE Select	NP_055573.3:p.Leu911Ser
NR_144939.2:n.3357T>C