Canonical Allele Identifier: CA383457687

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750569C>A (hg19) ; chr11:g.130880674C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880674C>A , CM000673.2:g.130880674C>A	GRCh38
NC_000011.9:g.130750569C>A , CM000673.1:g.130750569C>A	GRCh37
NC_000011.8:g.130255779C>A	NCBI36
NG_053190.1:g.40815G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2706G>T MANE Select	ENSP00000265909.4:p.Gln902His
ENST00000265909.8:c.2706G>T	ENSP00000265909.4:p.Gln902His
ENST00000426933.6:c.210G>T	ENSP00000413345.2:p.Gln70His
ENST00000526579.5:n.178-963G>T
ENST00000527116.5:n.468G>T
ENST00000528555.5:c.846G>T	ENSP00000435122.1:p.Gln282His
ENST00000530330.1:n.442G>T
ENST00000530356.5:c.846G>T	ENSP00000432307.1:p.Gln282His
ENST00000533318.5:n.1066G>T
ENST00000534726.5:c.426G>T	ENSP00000433699.1:p.Gln142His
NM_001301089.1:c.846G>T	NP_001288018.1:p.Gln282His
NM_014758.2:c.2706G>T	NP_055573.2:p.Gln902His
XM_005271546.3:c.2574-963G>T	XP_005271603.1:n.2574-963G>T
XM_011542819.1:c.2952G>T	XP_011541121.1:p.Gln984His
XM_011542820.1:c.2940G>T	XP_011541122.1:p.Gln980His
XM_011542821.1:c.2832G>T	XP_011541123.1:p.Gln944His
XM_011542824.1:c.2070G>T	XP_011541126.1:p.Gln690His
XM_011542825.1:c.1227G>T	XP_011541127.1:p.Gln409His
XM_011542826.1:c.1092G>T	XP_011541128.1:p.Gln364His
XM_011542827.1:c.972G>T	XP_011541129.1:p.Gln324His
NM_001347918.1:c.2586G>T	NP_001334847.1:p.Gln862His
NM_001347919.1:c.2574-963G>T	NP_001334848.1:n.2574-963G>T
NM_001347922.1:c.1035G>T	NP_001334851.1:p.Gln345His
NM_001347923.1:c.981G>T	NP_001334852.1:p.Gln327His
NM_001347924.1:c.726G>T	NP_001334853.1:p.Gln242His
NM_001347925.1:c.672G>T	NP_001334854.1:p.Gln224His
NM_001347926.1:c.714-963G>T	NP_001334855.1:n.714-963G>T
NM_001347927.1:c.426G>T	NP_001334856.1:p.Gln142His
NR_144939.1:n.3339G>T
XM_011542820.2:c.2940G>T	XP_011541122.1:p.Gln980His
XM_011542821.3:c.2832G>T	XP_011541123.1:p.Gln944His
XM_011542824.2:c.2070G>T	XP_011541126.1:p.Gln690His
XM_011542825.2:c.1227G>T	XP_011541127.1:p.Gln409His
XM_011542826.2:c.1092G>T	XP_011541128.1:p.Gln364His
XM_024448521.1:c.2952G>T	XP_024304289.1:p.Gln984His
XR_001747870.1:n.3777G>T
XR_001747872.1:n.3123G>T
XR_001747873.1:n.3437G>T
NM_001301089.2:c.846G>T	NP_001288018.1:p.Gln282His
NM_001347918.2:c.2586G>T	NP_001334847.2:p.Gln862His
NM_001347919.2:c.2574-963G>T	NP_001334848.2:n.2574-963G>T
NM_001347920.2:c.*21102G>T	NP_001334849.2:n.*21102G>T
NM_001347922.2:c.1035G>T	NP_001334851.2:p.Gln345His
NM_001347923.2:c.981G>T	NP_001334852.2:p.Gln327His
NM_001347924.2:c.726G>T	NP_001334853.1:p.Gln242His
NM_001347925.2:c.672G>T	NP_001334854.1:p.Gln224His
NM_001347926.2:c.714-963G>T	NP_001334855.1:n.714-963G>T
NM_001347927.2:c.426G>T	NP_001334856.1:p.Gln142His
NM_014758.3:c.2706G>T MANE Select	NP_055573.3:p.Gln902His
NR_144939.2:n.3331G>T