Canonical Allele Identifier: CA383457653

Gene: SNX19

Linked Data

• dbSNP Id: rs1485710978
• gnomAD v2: 11-130750553-T-C
• gnomAD v4: 11-130880658-T-C
• MyVariant Identifiers: chr11:g.130750553T>C (hg19) ; chr11:g.130880658T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880658T>C , CM000673.2:g.130880658T>C	GRCh38
NC_000011.9:g.130750553T>C , CM000673.1:g.130750553T>C	GRCh37
NC_000011.8:g.130255763T>C	NCBI36
NG_053190.1:g.40831A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2722A>G MANE Select	ENSP00000265909.4:p.Lys908Glu
ENST00000265909.8:c.2722A>G	ENSP00000265909.4:p.Lys908Glu
ENST00000426933.6:c.226A>G	ENSP00000413345.2:p.Lys76Glu
ENST00000526579.5:n.178-947A>G
ENST00000527116.5:n.484A>G
ENST00000528555.5:c.862A>G	ENSP00000435122.1:p.Lys288Glu
ENST00000530330.1:n.458A>G
ENST00000530356.5:c.862A>G	ENSP00000432307.1:p.Lys288Glu
ENST00000533318.5:n.1082A>G
ENST00000534726.5:c.442A>G	ENSP00000433699.1:p.Lys148Glu
NM_001301089.1:c.862A>G	NP_001288018.1:p.Lys288Glu
NM_014758.2:c.2722A>G	NP_055573.2:p.Lys908Glu
XM_005271546.3:c.2574-947A>G	XP_005271603.1:n.2574-947A>G
XM_011542819.1:c.2968A>G	XP_011541121.1:p.Lys990Glu
XM_011542820.1:c.2956A>G	XP_011541122.1:p.Lys986Glu
XM_011542821.1:c.2848A>G	XP_011541123.1:p.Lys950Glu
XM_011542824.1:c.2086A>G	XP_011541126.1:p.Lys696Glu
XM_011542825.1:c.1243A>G	XP_011541127.1:p.Lys415Glu
XM_011542826.1:c.1108A>G	XP_011541128.1:p.Lys370Glu
XM_011542827.1:c.988A>G	XP_011541129.1:p.Lys330Glu
NM_001347918.1:c.2602A>G	NP_001334847.1:p.Lys868Glu
NM_001347919.1:c.2574-947A>G	NP_001334848.1:n.2574-947A>G
NM_001347922.1:c.1051A>G	NP_001334851.1:p.Lys351Glu
NM_001347923.1:c.997A>G	NP_001334852.1:p.Lys333Glu
NM_001347924.1:c.742A>G	NP_001334853.1:p.Lys248Glu
NM_001347925.1:c.688A>G	NP_001334854.1:p.Lys230Glu
NM_001347926.1:c.714-947A>G	NP_001334855.1:n.714-947A>G
NM_001347927.1:c.442A>G	NP_001334856.1:p.Lys148Glu
NR_144939.1:n.3355A>G
XM_011542820.2:c.2956A>G	XP_011541122.1:p.Lys986Glu
XM_011542821.3:c.2848A>G	XP_011541123.1:p.Lys950Glu
XM_011542824.2:c.2086A>G	XP_011541126.1:p.Lys696Glu
XM_011542825.2:c.1243A>G	XP_011541127.1:p.Lys415Glu
XM_011542826.2:c.1108A>G	XP_011541128.1:p.Lys370Glu
XM_024448521.1:c.2968A>G	XP_024304289.1:p.Lys990Glu
XR_001747870.1:n.3793A>G
XR_001747872.1:n.3139A>G
XR_001747873.1:n.3453A>G
NM_001301089.2:c.862A>G	NP_001288018.1:p.Lys288Glu
NM_001347918.2:c.2602A>G	NP_001334847.2:p.Lys868Glu
NM_001347919.2:c.2574-947A>G	NP_001334848.2:n.2574-947A>G
NM_001347920.2:c.*21118A>G	NP_001334849.2:n.*21118A>G
NM_001347922.2:c.1051A>G	NP_001334851.2:p.Lys351Glu
NM_001347923.2:c.997A>G	NP_001334852.2:p.Lys333Glu
NM_001347924.2:c.742A>G	NP_001334853.1:p.Lys248Glu
NM_001347925.2:c.688A>G	NP_001334854.1:p.Lys230Glu
NM_001347926.2:c.714-947A>G	NP_001334855.1:n.714-947A>G
NM_001347927.2:c.442A>G	NP_001334856.1:p.Lys148Glu
NM_014758.3:c.2722A>G MANE Select	NP_055573.3:p.Lys908Glu
NR_144939.2:n.3347A>G