Canonical Allele Identifier: CA477582257

Gene: SNX19

Linked Data

• gnomAD v4: 11-130880649-A-G
• MyVariant Identifiers: chr11:g.130750544A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880649A>G , CM000673.2:g.130880649A>G	GRCh38
NC_000011.9:g.130750544A>G , CM000673.1:g.130750544A>G	GRCh37
NC_000011.8:g.130255754A>G	NCBI36
NG_053190.1:g.40840T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2731T>C MANE Select	ENSP00000265909.4:p.Leu911=
ENST00000265909.8:c.2731T>C	ENSP00000265909.4:p.Leu911=
ENST00000426933.6:c.235T>C	ENSP00000413345.2:p.Leu79=
ENST00000526579.5:n.178-938T>C
ENST00000527116.5:n.493T>C
ENST00000528555.5:c.871T>C	ENSP00000435122.1:p.Leu291=
ENST00000530330.1:n.467T>C
ENST00000530356.5:c.871T>C	ENSP00000432307.1:p.Leu291=
ENST00000533318.5:n.1091T>C
ENST00000534726.5:c.451T>C	ENSP00000433699.1:p.Leu151=
NM_001301089.1:c.871T>C	NP_001288018.1:p.Leu291=
NM_014758.2:c.2731T>C	NP_055573.2:p.Leu911=
XM_005271546.3:c.2574-938T>C	XP_005271603.1:n.2574-938T>C
XM_011542819.1:c.2977T>C	XP_011541121.1:p.Leu993=
XM_011542820.1:c.2965T>C	XP_011541122.1:p.Leu989=
XM_011542821.1:c.2857T>C	XP_011541123.1:p.Leu953=
XM_011542824.1:c.2095T>C	XP_011541126.1:p.Leu699=
XM_011542825.1:c.1252T>C	XP_011541127.1:p.Leu418=
XM_011542826.1:c.1117T>C	XP_011541128.1:p.Leu373=
XM_011542827.1:c.997T>C	XP_011541129.1:p.Leu333=
NM_001347918.1:c.2611T>C	NP_001334847.1:p.Leu871=
NM_001347919.1:c.2574-938T>C	NP_001334848.1:n.2574-938T>C
NM_001347922.1:c.1060T>C	NP_001334851.1:p.Leu354=
NM_001347923.1:c.1006T>C	NP_001334852.1:p.Leu336=
NM_001347924.1:c.751T>C	NP_001334853.1:p.Leu251=
NM_001347925.1:c.697T>C	NP_001334854.1:p.Leu233=
NM_001347926.1:c.714-938T>C	NP_001334855.1:n.714-938T>C
NM_001347927.1:c.451T>C	NP_001334856.1:p.Leu151=
NR_144939.1:n.3364T>C
XM_011542820.2:c.2965T>C	XP_011541122.1:p.Leu989=
XM_011542821.3:c.2857T>C	XP_011541123.1:p.Leu953=
XM_011542824.2:c.2095T>C	XP_011541126.1:p.Leu699=
XM_011542825.2:c.1252T>C	XP_011541127.1:p.Leu418=
XM_011542826.2:c.1117T>C	XP_011541128.1:p.Leu373=
XM_024448521.1:c.2977T>C	XP_024304289.1:p.Leu993=
XR_001747870.1:n.3802T>C
XR_001747872.1:n.3148T>C
XR_001747873.1:n.3462T>C
NM_001301089.2:c.871T>C	NP_001288018.1:p.Leu291=
NM_001347918.2:c.2611T>C	NP_001334847.2:p.Leu871=
NM_001347919.2:c.2574-938T>C	NP_001334848.2:n.2574-938T>C
NM_001347920.2:c.*21127T>C	NP_001334849.2:n.*21127T>C
NM_001347922.2:c.1060T>C	NP_001334851.2:p.Leu354=
NM_001347923.2:c.1006T>C	NP_001334852.2:p.Leu336=
NM_001347924.2:c.751T>C	NP_001334853.1:p.Leu251=
NM_001347925.2:c.697T>C	NP_001334854.1:p.Leu233=
NM_001347926.2:c.714-938T>C	NP_001334855.1:n.714-938T>C
NM_001347927.2:c.451T>C	NP_001334856.1:p.Leu151=
NM_014758.3:c.2731T>C MANE Select	NP_055573.3:p.Leu911=
NR_144939.2:n.3356T>C