Canonical Allele Identifier: CA383457738

Gene: SNX19

Linked Data

• dbSNP Id: rs1943595293
• MyVariant Identifiers: chr11:g.130750594G>T (hg19) ; chr11:g.130880699G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880699G>T , CM000673.2:g.130880699G>T	GRCh38
NC_000011.9:g.130750594G>T , CM000673.1:g.130750594G>T	GRCh37
NC_000011.8:g.130255804G>T	NCBI36
NG_053190.1:g.40790C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2681C>A MANE Select	ENSP00000265909.4:p.Pro894Gln
ENST00000265909.8:c.2681C>A	ENSP00000265909.4:p.Pro894Gln
ENST00000426933.6:c.185C>A	ENSP00000413345.2:p.Pro62Gln
ENST00000526579.5:n.178-988C>A
ENST00000527116.5:n.443C>A
ENST00000528555.5:c.821C>A	ENSP00000435122.1:p.Pro274Gln
ENST00000530330.1:n.417C>A
ENST00000530356.5:c.821C>A	ENSP00000432307.1:p.Pro274Gln
ENST00000533318.5:n.1041C>A
ENST00000534726.5:c.401C>A	ENSP00000433699.1:p.Pro134Gln
NM_001301089.1:c.821C>A	NP_001288018.1:p.Pro274Gln
NM_014758.2:c.2681C>A	NP_055573.2:p.Pro894Gln
XM_005271546.3:c.2574-988C>A	XP_005271603.1:n.2574-988C>A
XM_011542819.1:c.2927C>A	XP_011541121.1:p.Pro976Gln
XM_011542820.1:c.2915C>A	XP_011541122.1:p.Pro972Gln
XM_011542821.1:c.2807C>A	XP_011541123.1:p.Pro936Gln
XM_011542824.1:c.2045C>A	XP_011541126.1:p.Pro682Gln
XM_011542825.1:c.1202C>A	XP_011541127.1:p.Pro401Gln
XM_011542826.1:c.1067C>A	XP_011541128.1:p.Pro356Gln
XM_011542827.1:c.947C>A	XP_011541129.1:p.Pro316Gln
NM_001347918.1:c.2561C>A	NP_001334847.1:p.Pro854Gln
NM_001347919.1:c.2574-988C>A	NP_001334848.1:n.2574-988C>A
NM_001347922.1:c.1010C>A	NP_001334851.1:p.Pro337Gln
NM_001347923.1:c.956C>A	NP_001334852.1:p.Pro319Gln
NM_001347924.1:c.701C>A	NP_001334853.1:p.Pro234Gln
NM_001347925.1:c.647C>A	NP_001334854.1:p.Pro216Gln
NM_001347926.1:c.714-988C>A	NP_001334855.1:n.714-988C>A
NM_001347927.1:c.401C>A	NP_001334856.1:p.Pro134Gln
NR_144939.1:n.3314C>A
XM_011542820.2:c.2915C>A	XP_011541122.1:p.Pro972Gln
XM_011542821.3:c.2807C>A	XP_011541123.1:p.Pro936Gln
XM_011542824.2:c.2045C>A	XP_011541126.1:p.Pro682Gln
XM_011542825.2:c.1202C>A	XP_011541127.1:p.Pro401Gln
XM_011542826.2:c.1067C>A	XP_011541128.1:p.Pro356Gln
XM_024448521.1:c.2927C>A	XP_024304289.1:p.Pro976Gln
XR_001747870.1:n.3752C>A
XR_001747872.1:n.3098C>A
XR_001747873.1:n.3412C>A
NM_001301089.2:c.821C>A	NP_001288018.1:p.Pro274Gln
NM_001347918.2:c.2561C>A	NP_001334847.2:p.Pro854Gln
NM_001347919.2:c.2574-988C>A	NP_001334848.2:n.2574-988C>A
NM_001347920.2:c.*21077C>A	NP_001334849.2:n.*21077C>A
NM_001347922.2:c.1010C>A	NP_001334851.2:p.Pro337Gln
NM_001347923.2:c.956C>A	NP_001334852.2:p.Pro319Gln
NM_001347924.2:c.701C>A	NP_001334853.1:p.Pro234Gln
NM_001347925.2:c.647C>A	NP_001334854.1:p.Pro216Gln
NM_001347926.2:c.714-988C>A	NP_001334855.1:n.714-988C>A
NM_001347927.2:c.401C>A	NP_001334856.1:p.Pro134Gln
NM_014758.3:c.2681C>A MANE Select	NP_055573.3:p.Pro894Gln
NR_144939.2:n.3306C>A