Canonical Allele Identifier: CA383457624

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750541G>A (hg19) ; chr11:g.130880646G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880646G>A , CM000673.2:g.130880646G>A	GRCh38
NC_000011.9:g.130750541G>A , CM000673.1:g.130750541G>A	GRCh37
NC_000011.8:g.130255751G>A	NCBI36
NG_053190.1:g.40843C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2734C>T MANE Select	ENSP00000265909.4:p.Gln912Ter
ENST00000265909.8:c.2734C>T	ENSP00000265909.4:p.Gln912Ter
ENST00000426933.6:c.238C>T	ENSP00000413345.2:p.Gln80Ter
ENST00000526579.5:n.178-935C>T
ENST00000527116.5:n.496C>T
ENST00000528555.5:c.874C>T	ENSP00000435122.1:p.Gln292Ter
ENST00000530330.1:n.470C>T
ENST00000530356.5:c.874C>T	ENSP00000432307.1:p.Gln292Ter
ENST00000533318.5:n.1094C>T
ENST00000534726.5:c.454C>T	ENSP00000433699.1:p.Gln152Ter
NM_001301089.1:c.874C>T	NP_001288018.1:p.Gln292Ter
NM_014758.2:c.2734C>T	NP_055573.2:p.Gln912Ter
XM_005271546.3:c.2574-935C>T	XP_005271603.1:n.2574-935C>T
XM_011542819.1:c.2980C>T	XP_011541121.1:p.Gln994Ter
XM_011542820.1:c.2968C>T	XP_011541122.1:p.Gln990Ter
XM_011542821.1:c.2860C>T	XP_011541123.1:p.Gln954Ter
XM_011542824.1:c.2098C>T	XP_011541126.1:p.Gln700Ter
XM_011542825.1:c.1255C>T	XP_011541127.1:p.Gln419Ter
XM_011542826.1:c.1120C>T	XP_011541128.1:p.Gln374Ter
XM_011542827.1:c.1000C>T	XP_011541129.1:p.Gln334Ter
NM_001347918.1:c.2614C>T	NP_001334847.1:p.Gln872Ter
NM_001347919.1:c.2574-935C>T	NP_001334848.1:n.2574-935C>T
NM_001347922.1:c.1063C>T	NP_001334851.1:p.Gln355Ter
NM_001347923.1:c.1009C>T	NP_001334852.1:p.Gln337Ter
NM_001347924.1:c.754C>T	NP_001334853.1:p.Gln252Ter
NM_001347925.1:c.700C>T	NP_001334854.1:p.Gln234Ter
NM_001347926.1:c.714-935C>T	NP_001334855.1:n.714-935C>T
NM_001347927.1:c.454C>T	NP_001334856.1:p.Gln152Ter
NR_144939.1:n.3367C>T
XM_011542820.2:c.2968C>T	XP_011541122.1:p.Gln990Ter
XM_011542821.3:c.2860C>T	XP_011541123.1:p.Gln954Ter
XM_011542824.2:c.2098C>T	XP_011541126.1:p.Gln700Ter
XM_011542825.2:c.1255C>T	XP_011541127.1:p.Gln419Ter
XM_011542826.2:c.1120C>T	XP_011541128.1:p.Gln374Ter
XM_024448521.1:c.2980C>T	XP_024304289.1:p.Gln994Ter
XR_001747870.1:n.3805C>T
XR_001747872.1:n.3151C>T
XR_001747873.1:n.3465C>T
NM_001301089.2:c.874C>T	NP_001288018.1:p.Gln292Ter
NM_001347918.2:c.2614C>T	NP_001334847.2:p.Gln872Ter
NM_001347919.2:c.2574-935C>T	NP_001334848.2:n.2574-935C>T
NM_001347920.2:c.*21130C>T	NP_001334849.2:n.*21130C>T
NM_001347922.2:c.1063C>T	NP_001334851.2:p.Gln355Ter
NM_001347923.2:c.1009C>T	NP_001334852.2:p.Gln337Ter
NM_001347924.2:c.754C>T	NP_001334853.1:p.Gln252Ter
NM_001347925.2:c.700C>T	NP_001334854.1:p.Gln234Ter
NM_001347926.2:c.714-935C>T	NP_001334855.1:n.714-935C>T
NM_001347927.2:c.454C>T	NP_001334856.1:p.Gln152Ter
NM_014758.3:c.2734C>T MANE Select	NP_055573.3:p.Gln912Ter
NR_144939.2:n.3359C>T