Canonical Allele Identifier: CA2616844390

Gene: SNX19

Linked Data

• gnomAD v4: 11-130880698-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880700del , CM000673.2:g.130880700del	GRCh38
NC_000011.9:g.130750595del , CM000673.1:g.130750595del	GRCh37
NC_000011.8:g.130255805del	NCBI36
NG_053190.1:g.40790del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2681del MANE Select	ENSP00000265909.4:p.Pro894HisfsTer4
ENST00000265909.8:c.2681del	ENSP00000265909.4:p.Pro894HisfsTer4
ENST00000426933.6:c.185del	ENSP00000413345.2:p.Pro62HisfsTer4
ENST00000526579.5:n.178-988del
ENST00000527116.5:n.443del
ENST00000528555.5:c.821del	ENSP00000435122.1:p.Pro274HisfsTer4
ENST00000530330.1:n.417del
ENST00000530356.5:c.821del	ENSP00000432307.1:p.Pro274HisfsTer4
ENST00000533318.5:n.1041del
ENST00000534726.5:c.401del	ENSP00000433699.1:p.Pro134HisfsTer4
NM_001301089.1:c.821del	NP_001288018.1:p.Pro274HisfsTer4
NM_014758.2:c.2681del	NP_055573.2:p.Pro894HisfsTer4
XM_005271546.3:c.2574-988del	XP_005271603.1:n.2574-988del
XM_011542819.1:c.2927del	XP_011541121.1:p.Pro976HisfsTer4
XM_011542820.1:c.2915del	XP_011541122.1:p.Pro972HisfsTer4
XM_011542821.1:c.2807del	XP_011541123.1:p.Pro936HisfsTer4
XM_011542824.1:c.2045del	XP_011541126.1:p.Pro682HisfsTer4
XM_011542825.1:c.1202del	XP_011541127.1:p.Pro401HisfsTer4
XM_011542826.1:c.1067del	XP_011541128.1:p.Pro356HisfsTer4
XM_011542827.1:c.947del	XP_011541129.1:p.Pro316HisfsTer4
NM_001347918.1:c.2561del	NP_001334847.1:p.Pro854HisfsTer4
NM_001347919.1:c.2574-988del	NP_001334848.1:n.2574-988del
NM_001347922.1:c.1010del	NP_001334851.1:p.Pro337HisfsTer4
NM_001347923.1:c.956del	NP_001334852.1:p.Pro319HisfsTer4
NM_001347924.1:c.701del	NP_001334853.1:p.Pro234HisfsTer4
NM_001347925.1:c.647del	NP_001334854.1:p.Pro216HisfsTer4
NM_001347926.1:c.714-988del	NP_001334855.1:n.714-988del
NM_001347927.1:c.401del	NP_001334856.1:p.Pro134HisfsTer4
NR_144939.1:n.3314del
XM_011542820.2:c.2915del	XP_011541122.1:p.Pro972HisfsTer4
XM_011542821.3:c.2807del	XP_011541123.1:p.Pro936HisfsTer4
XM_011542824.2:c.2045del	XP_011541126.1:p.Pro682HisfsTer4
XM_011542825.2:c.1202del	XP_011541127.1:p.Pro401HisfsTer4
XM_011542826.2:c.1067del	XP_011541128.1:p.Pro356HisfsTer4
XM_024448521.1:c.2927del	XP_024304289.1:p.Pro976HisfsTer4
XR_001747870.1:n.3752del
XR_001747872.1:n.3098del
XR_001747873.1:n.3412del
NM_001301089.2:c.821del	NP_001288018.1:p.Pro274HisfsTer4
NM_001347918.2:c.2561del	NP_001334847.2:p.Pro854HisfsTer4
NM_001347919.2:c.2574-988del	NP_001334848.2:n.2574-988del
NM_001347920.2:c.*21077del	NP_001334849.2:n.*21077del
NM_001347922.2:c.1010del	NP_001334851.2:p.Pro337HisfsTer4
NM_001347923.2:c.956del	NP_001334852.2:p.Pro319HisfsTer4
NM_001347924.2:c.701del	NP_001334853.1:p.Pro234HisfsTer4
NM_001347925.2:c.647del	NP_001334854.1:p.Pro216HisfsTer4
NM_001347926.2:c.714-988del	NP_001334855.1:n.714-988del
NM_001347927.2:c.401del	NP_001334856.1:p.Pro134HisfsTer4
NM_014758.3:c.2681del MANE Select	NP_055573.3:p.Pro894HisfsTer4
NR_144939.2:n.3306del