Canonical Allele Identifier: CA383457723

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750585A>G (hg19) ; chr11:g.130880690A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880690A>G , CM000673.2:g.130880690A>G	GRCh38
NC_000011.9:g.130750585A>G , CM000673.1:g.130750585A>G	GRCh37
NC_000011.8:g.130255795A>G	NCBI36
NG_053190.1:g.40799T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2690T>C MANE Select	ENSP00000265909.4:p.Val897Ala
ENST00000265909.8:c.2690T>C	ENSP00000265909.4:p.Val897Ala
ENST00000426933.6:c.194T>C	ENSP00000413345.2:p.Val65Ala
ENST00000526579.5:n.178-979T>C
ENST00000527116.5:n.452T>C
ENST00000528555.5:c.830T>C	ENSP00000435122.1:p.Val277Ala
ENST00000530330.1:n.426T>C
ENST00000530356.5:c.830T>C	ENSP00000432307.1:p.Val277Ala
ENST00000533318.5:n.1050T>C
ENST00000534726.5:c.410T>C	ENSP00000433699.1:p.Val137Ala
NM_001301089.1:c.830T>C	NP_001288018.1:p.Val277Ala
NM_014758.2:c.2690T>C	NP_055573.2:p.Val897Ala
XM_005271546.3:c.2574-979T>C	XP_005271603.1:n.2574-979T>C
XM_011542819.1:c.2936T>C	XP_011541121.1:p.Val979Ala
XM_011542820.1:c.2924T>C	XP_011541122.1:p.Val975Ala
XM_011542821.1:c.2816T>C	XP_011541123.1:p.Val939Ala
XM_011542824.1:c.2054T>C	XP_011541126.1:p.Val685Ala
XM_011542825.1:c.1211T>C	XP_011541127.1:p.Val404Ala
XM_011542826.1:c.1076T>C	XP_011541128.1:p.Val359Ala
XM_011542827.1:c.956T>C	XP_011541129.1:p.Val319Ala
NM_001347918.1:c.2570T>C	NP_001334847.1:p.Val857Ala
NM_001347919.1:c.2574-979T>C	NP_001334848.1:n.2574-979T>C
NM_001347922.1:c.1019T>C	NP_001334851.1:p.Val340Ala
NM_001347923.1:c.965T>C	NP_001334852.1:p.Val322Ala
NM_001347924.1:c.710T>C	NP_001334853.1:p.Val237Ala
NM_001347925.1:c.656T>C	NP_001334854.1:p.Val219Ala
NM_001347926.1:c.714-979T>C	NP_001334855.1:n.714-979T>C
NM_001347927.1:c.410T>C	NP_001334856.1:p.Val137Ala
NR_144939.1:n.3323T>C
XM_011542820.2:c.2924T>C	XP_011541122.1:p.Val975Ala
XM_011542821.3:c.2816T>C	XP_011541123.1:p.Val939Ala
XM_011542824.2:c.2054T>C	XP_011541126.1:p.Val685Ala
XM_011542825.2:c.1211T>C	XP_011541127.1:p.Val404Ala
XM_011542826.2:c.1076T>C	XP_011541128.1:p.Val359Ala
XM_024448521.1:c.2936T>C	XP_024304289.1:p.Val979Ala
XR_001747870.1:n.3761T>C
XR_001747872.1:n.3107T>C
XR_001747873.1:n.3421T>C
NM_001301089.2:c.830T>C	NP_001288018.1:p.Val277Ala
NM_001347918.2:c.2570T>C	NP_001334847.2:p.Val857Ala
NM_001347919.2:c.2574-979T>C	NP_001334848.2:n.2574-979T>C
NM_001347920.2:c.*21086T>C	NP_001334849.2:n.*21086T>C
NM_001347922.2:c.1019T>C	NP_001334851.2:p.Val340Ala
NM_001347923.2:c.965T>C	NP_001334852.2:p.Val322Ala
NM_001347924.2:c.710T>C	NP_001334853.1:p.Val237Ala
NM_001347925.2:c.656T>C	NP_001334854.1:p.Val219Ala
NM_001347926.2:c.714-979T>C	NP_001334855.1:n.714-979T>C
NM_001347927.2:c.410T>C	NP_001334856.1:p.Val137Ala
NM_014758.3:c.2690T>C MANE Select	NP_055573.3:p.Val897Ala
NR_144939.2:n.3315T>C