Canonical Allele Identifier: CA383457586

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750525A>C (hg19) ; chr11:g.130880630A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880630A>C , CM000673.2:g.130880630A>C	GRCh38
NC_000011.9:g.130750525A>C , CM000673.1:g.130750525A>C	GRCh37
NC_000011.8:g.130255735A>C	NCBI36
NG_053190.1:g.40859T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2750T>G MANE Select	ENSP00000265909.4:p.Val917Gly
ENST00000265909.8:c.2750T>G	ENSP00000265909.4:p.Val917Gly
ENST00000426933.6:c.254T>G	ENSP00000413345.2:p.Val85Gly
ENST00000526579.5:n.178-919T>G
ENST00000527116.5:n.512T>G
ENST00000528555.5:c.890T>G	ENSP00000435122.1:p.Val297Gly
ENST00000530330.1:n.486T>G
ENST00000530356.5:c.890T>G	ENSP00000432307.1:p.Val297Gly
ENST00000533318.5:n.1110T>G
ENST00000534726.5:c.470T>G	ENSP00000433699.1:p.Val157Gly
NM_001301089.1:c.890T>G	NP_001288018.1:p.Val297Gly
NM_014758.2:c.2750T>G	NP_055573.2:p.Val917Gly
XM_005271546.3:c.2574-919T>G	XP_005271603.1:n.2574-919T>G
XM_011542819.1:c.2996T>G	XP_011541121.1:p.Val999Gly
XM_011542820.1:c.2984T>G	XP_011541122.1:p.Val995Gly
XM_011542821.1:c.2876T>G	XP_011541123.1:p.Val959Gly
XM_011542824.1:c.2114T>G	XP_011541126.1:p.Val705Gly
XM_011542825.1:c.1271T>G	XP_011541127.1:p.Val424Gly
XM_011542826.1:c.1136T>G	XP_011541128.1:p.Val379Gly
XM_011542827.1:c.1016T>G	XP_011541129.1:p.Val339Gly
NM_001347918.1:c.2630T>G	NP_001334847.1:p.Val877Gly
NM_001347919.1:c.2574-919T>G	NP_001334848.1:n.2574-919T>G
NM_001347922.1:c.1079T>G	NP_001334851.1:p.Val360Gly
NM_001347923.1:c.1025T>G	NP_001334852.1:p.Val342Gly
NM_001347924.1:c.770T>G	NP_001334853.1:p.Val257Gly
NM_001347925.1:c.716T>G	NP_001334854.1:p.Val239Gly
NM_001347926.1:c.714-919T>G	NP_001334855.1:n.714-919T>G
NM_001347927.1:c.470T>G	NP_001334856.1:p.Val157Gly
NR_144939.1:n.3383T>G
XM_011542820.2:c.2984T>G	XP_011541122.1:p.Val995Gly
XM_011542821.3:c.2876T>G	XP_011541123.1:p.Val959Gly
XM_011542824.2:c.2114T>G	XP_011541126.1:p.Val705Gly
XM_011542825.2:c.1271T>G	XP_011541127.1:p.Val424Gly
XM_011542826.2:c.1136T>G	XP_011541128.1:p.Val379Gly
XM_024448521.1:c.2996T>G	XP_024304289.1:p.Val999Gly
XR_001747870.1:n.3821T>G
XR_001747872.1:n.3167T>G
XR_001747873.1:n.3481T>G
NM_001301089.2:c.890T>G	NP_001288018.1:p.Val297Gly
NM_001347918.2:c.2630T>G	NP_001334847.2:p.Val877Gly
NM_001347919.2:c.2574-919T>G	NP_001334848.2:n.2574-919T>G
NM_001347920.2:c.*21146T>G	NP_001334849.2:n.*21146T>G
NM_001347922.2:c.1079T>G	NP_001334851.2:p.Val360Gly
NM_001347923.2:c.1025T>G	NP_001334852.2:p.Val342Gly
NM_001347924.2:c.770T>G	NP_001334853.1:p.Val257Gly
NM_001347925.2:c.716T>G	NP_001334854.1:p.Val239Gly
NM_001347926.2:c.714-919T>G	NP_001334855.1:n.714-919T>G
NM_001347927.2:c.470T>G	NP_001334856.1:p.Val157Gly
NM_014758.3:c.2750T>G MANE Select	NP_055573.3:p.Val917Gly
NR_144939.2:n.3375T>G