Canonical Allele Identifier: CA477582249

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750527T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880632T>G , CM000673.2:g.130880632T>G	GRCh38
NC_000011.9:g.130750527T>G , CM000673.1:g.130750527T>G	GRCh37
NC_000011.8:g.130255737T>G	NCBI36
NG_053190.1:g.40857A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2748A>C MANE Select	ENSP00000265909.4:p.Gly916=
ENST00000265909.8:c.2748A>C	ENSP00000265909.4:p.Gly916=
ENST00000426933.6:c.252A>C	ENSP00000413345.2:p.Gly84=
ENST00000526579.5:n.178-921A>C
ENST00000527116.5:n.510A>C
ENST00000528555.5:c.888A>C	ENSP00000435122.1:p.Gly296=
ENST00000530330.1:n.484A>C
ENST00000530356.5:c.888A>C	ENSP00000432307.1:p.Gly296=
ENST00000533318.5:n.1108A>C
ENST00000534726.5:c.468A>C	ENSP00000433699.1:p.Gly156=
NM_001301089.1:c.888A>C	NP_001288018.1:p.Gly296=
NM_014758.2:c.2748A>C	NP_055573.2:p.Gly916=
XM_005271546.3:c.2574-921A>C	XP_005271603.1:n.2574-921A>C
XM_011542819.1:c.2994A>C	XP_011541121.1:p.Gly998=
XM_011542820.1:c.2982A>C	XP_011541122.1:p.Gly994=
XM_011542821.1:c.2874A>C	XP_011541123.1:p.Gly958=
XM_011542824.1:c.2112A>C	XP_011541126.1:p.Gly704=
XM_011542825.1:c.1269A>C	XP_011541127.1:p.Gly423=
XM_011542826.1:c.1134A>C	XP_011541128.1:p.Gly378=
XM_011542827.1:c.1014A>C	XP_011541129.1:p.Gly338=
NM_001347918.1:c.2628A>C	NP_001334847.1:p.Gly876=
NM_001347919.1:c.2574-921A>C	NP_001334848.1:n.2574-921A>C
NM_001347922.1:c.1077A>C	NP_001334851.1:p.Gly359=
NM_001347923.1:c.1023A>C	NP_001334852.1:p.Gly341=
NM_001347924.1:c.768A>C	NP_001334853.1:p.Gly256=
NM_001347925.1:c.714A>C	NP_001334854.1:p.Gly238=
NM_001347926.1:c.714-921A>C	NP_001334855.1:n.714-921A>C
NM_001347927.1:c.468A>C	NP_001334856.1:p.Gly156=
NR_144939.1:n.3381A>C
XM_011542820.2:c.2982A>C	XP_011541122.1:p.Gly994=
XM_011542821.3:c.2874A>C	XP_011541123.1:p.Gly958=
XM_011542824.2:c.2112A>C	XP_011541126.1:p.Gly704=
XM_011542825.2:c.1269A>C	XP_011541127.1:p.Gly423=
XM_011542826.2:c.1134A>C	XP_011541128.1:p.Gly378=
XM_024448521.1:c.2994A>C	XP_024304289.1:p.Gly998=
XR_001747870.1:n.3819A>C
XR_001747872.1:n.3165A>C
XR_001747873.1:n.3479A>C
NM_001301089.2:c.888A>C	NP_001288018.1:p.Gly296=
NM_001347918.2:c.2628A>C	NP_001334847.2:p.Gly876=
NM_001347919.2:c.2574-921A>C	NP_001334848.2:n.2574-921A>C
NM_001347920.2:c.*21144A>C	NP_001334849.2:n.*21144A>C
NM_001347922.2:c.1077A>C	NP_001334851.2:p.Gly359=
NM_001347923.2:c.1023A>C	NP_001334852.2:p.Gly341=
NM_001347924.2:c.768A>C	NP_001334853.1:p.Gly256=
NM_001347925.2:c.714A>C	NP_001334854.1:p.Gly238=
NM_001347926.2:c.714-921A>C	NP_001334855.1:n.714-921A>C
NM_001347927.2:c.468A>C	NP_001334856.1:p.Gly156=
NM_014758.3:c.2748A>C MANE Select	NP_055573.3:p.Gly916=
NR_144939.2:n.3373A>C