Canonical Allele Identifier: CA383457619

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750539C>A (hg19) ; chr11:g.130880644C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880644C>A , CM000673.2:g.130880644C>A	GRCh38
NC_000011.9:g.130750539C>A , CM000673.1:g.130750539C>A	GRCh37
NC_000011.8:g.130255749C>A	NCBI36
NG_053190.1:g.40845G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2736G>T MANE Select	ENSP00000265909.4:p.Gln912His
ENST00000265909.8:c.2736G>T	ENSP00000265909.4:p.Gln912His
ENST00000426933.6:c.240G>T	ENSP00000413345.2:p.Gln80His
ENST00000526579.5:n.178-933G>T
ENST00000527116.5:n.498G>T
ENST00000528555.5:c.876G>T	ENSP00000435122.1:p.Gln292His
ENST00000530330.1:n.472G>T
ENST00000530356.5:c.876G>T	ENSP00000432307.1:p.Gln292His
ENST00000533318.5:n.1096G>T
ENST00000534726.5:c.456G>T	ENSP00000433699.1:p.Gln152His
NM_001301089.1:c.876G>T	NP_001288018.1:p.Gln292His
NM_014758.2:c.2736G>T	NP_055573.2:p.Gln912His
XM_005271546.3:c.2574-933G>T	XP_005271603.1:n.2574-933G>T
XM_011542819.1:c.2982G>T	XP_011541121.1:p.Gln994His
XM_011542820.1:c.2970G>T	XP_011541122.1:p.Gln990His
XM_011542821.1:c.2862G>T	XP_011541123.1:p.Gln954His
XM_011542824.1:c.2100G>T	XP_011541126.1:p.Gln700His
XM_011542825.1:c.1257G>T	XP_011541127.1:p.Gln419His
XM_011542826.1:c.1122G>T	XP_011541128.1:p.Gln374His
XM_011542827.1:c.1002G>T	XP_011541129.1:p.Gln334His
NM_001347918.1:c.2616G>T	NP_001334847.1:p.Gln872His
NM_001347919.1:c.2574-933G>T	NP_001334848.1:n.2574-933G>T
NM_001347922.1:c.1065G>T	NP_001334851.1:p.Gln355His
NM_001347923.1:c.1011G>T	NP_001334852.1:p.Gln337His
NM_001347924.1:c.756G>T	NP_001334853.1:p.Gln252His
NM_001347925.1:c.702G>T	NP_001334854.1:p.Gln234His
NM_001347926.1:c.714-933G>T	NP_001334855.1:n.714-933G>T
NM_001347927.1:c.456G>T	NP_001334856.1:p.Gln152His
NR_144939.1:n.3369G>T
XM_011542820.2:c.2970G>T	XP_011541122.1:p.Gln990His
XM_011542821.3:c.2862G>T	XP_011541123.1:p.Gln954His
XM_011542824.2:c.2100G>T	XP_011541126.1:p.Gln700His
XM_011542825.2:c.1257G>T	XP_011541127.1:p.Gln419His
XM_011542826.2:c.1122G>T	XP_011541128.1:p.Gln374His
XM_024448521.1:c.2982G>T	XP_024304289.1:p.Gln994His
XR_001747870.1:n.3807G>T
XR_001747872.1:n.3153G>T
XR_001747873.1:n.3467G>T
NM_001301089.2:c.876G>T	NP_001288018.1:p.Gln292His
NM_001347918.2:c.2616G>T	NP_001334847.2:p.Gln872His
NM_001347919.2:c.2574-933G>T	NP_001334848.2:n.2574-933G>T
NM_001347920.2:c.*21132G>T	NP_001334849.2:n.*21132G>T
NM_001347922.2:c.1065G>T	NP_001334851.2:p.Gln355His
NM_001347923.2:c.1011G>T	NP_001334852.2:p.Gln337His
NM_001347924.2:c.756G>T	NP_001334853.1:p.Gln252His
NM_001347925.2:c.702G>T	NP_001334854.1:p.Gln234His
NM_001347926.2:c.714-933G>T	NP_001334855.1:n.714-933G>T
NM_001347927.2:c.456G>T	NP_001334856.1:p.Gln152His
NM_014758.3:c.2736G>T MANE Select	NP_055573.3:p.Gln912His
NR_144939.2:n.3361G>T