Canonical Allele Identifier: CA477582239

Gene: SNX19

Linked Data

• gnomAD v4: 11-130880623-T-C
• MyVariant Identifiers: chr11:g.130750518T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880623T>C , CM000673.2:g.130880623T>C	GRCh38
NC_000011.9:g.130750518T>C , CM000673.1:g.130750518T>C	GRCh37
NC_000011.8:g.130255728T>C	NCBI36
NG_053190.1:g.40866A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2757A>G MANE Select	ENSP00000265909.4:p.Pro919=
ENST00000265909.8:c.2757A>G	ENSP00000265909.4:p.Pro919=
ENST00000426933.6:c.261A>G	ENSP00000413345.2:p.Pro87=
ENST00000526579.5:n.178-912A>G
ENST00000527116.5:n.519A>G
ENST00000528555.5:c.897A>G	ENSP00000435122.1:p.Pro299=
ENST00000530330.1:n.493A>G
ENST00000530356.5:c.897A>G	ENSP00000432307.1:p.Pro299=
ENST00000533318.5:n.1117A>G
ENST00000534726.5:c.477A>G	ENSP00000433699.1:p.Pro159=
NM_001301089.1:c.897A>G	NP_001288018.1:p.Pro299=
NM_014758.2:c.2757A>G	NP_055573.2:p.Pro919=
XM_005271546.3:c.2574-912A>G	XP_005271603.1:n.2574-912A>G
XM_011542819.1:c.3003A>G	XP_011541121.1:p.Pro1001=
XM_011542820.1:c.2991A>G	XP_011541122.1:p.Pro997=
XM_011542821.1:c.2883A>G	XP_011541123.1:p.Pro961=
XM_011542824.1:c.2121A>G	XP_011541126.1:p.Pro707=
XM_011542825.1:c.1278A>G	XP_011541127.1:p.Pro426=
XM_011542826.1:c.1143A>G	XP_011541128.1:p.Pro381=
XM_011542827.1:c.1023A>G	XP_011541129.1:p.Pro341=
NM_001347918.1:c.2637A>G	NP_001334847.1:p.Pro879=
NM_001347919.1:c.2574-912A>G	NP_001334848.1:n.2574-912A>G
NM_001347922.1:c.1086A>G	NP_001334851.1:p.Pro362=
NM_001347923.1:c.1032A>G	NP_001334852.1:p.Pro344=
NM_001347924.1:c.777A>G	NP_001334853.1:p.Pro259=
NM_001347925.1:c.723A>G	NP_001334854.1:p.Pro241=
NM_001347926.1:c.714-912A>G	NP_001334855.1:n.714-912A>G
NM_001347927.1:c.477A>G	NP_001334856.1:p.Pro159=
NR_144939.1:n.3390A>G
XM_011542820.2:c.2991A>G	XP_011541122.1:p.Pro997=
XM_011542821.3:c.2883A>G	XP_011541123.1:p.Pro961=
XM_011542824.2:c.2121A>G	XP_011541126.1:p.Pro707=
XM_011542825.2:c.1278A>G	XP_011541127.1:p.Pro426=
XM_011542826.2:c.1143A>G	XP_011541128.1:p.Pro381=
XM_024448521.1:c.3003A>G	XP_024304289.1:p.Pro1001=
XR_001747870.1:n.3828A>G
XR_001747872.1:n.3174A>G
XR_001747873.1:n.3488A>G
NM_001301089.2:c.897A>G	NP_001288018.1:p.Pro299=
NM_001347918.2:c.2637A>G	NP_001334847.2:p.Pro879=
NM_001347919.2:c.2574-912A>G	NP_001334848.2:n.2574-912A>G
NM_001347920.2:c.*21153A>G	NP_001334849.2:n.*21153A>G
NM_001347922.2:c.1086A>G	NP_001334851.2:p.Pro362=
NM_001347923.2:c.1032A>G	NP_001334852.2:p.Pro344=
NM_001347924.2:c.777A>G	NP_001334853.1:p.Pro259=
NM_001347925.2:c.723A>G	NP_001334854.1:p.Pro241=
NM_001347926.2:c.714-912A>G	NP_001334855.1:n.714-912A>G
NM_001347927.2:c.477A>G	NP_001334856.1:p.Pro159=
NM_014758.3:c.2757A>G MANE Select	NP_055573.3:p.Pro919=
NR_144939.2:n.3382A>G