Canonical Allele Identifier: CA383457729

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750588G>T (hg19) ; chr11:g.130880693G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880693G>T , CM000673.2:g.130880693G>T	GRCh38
NC_000011.9:g.130750588G>T , CM000673.1:g.130750588G>T	GRCh37
NC_000011.8:g.130255798G>T	NCBI36
NG_053190.1:g.40796C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2687C>A MANE Select	ENSP00000265909.4:p.Pro896His
ENST00000265909.8:c.2687C>A	ENSP00000265909.4:p.Pro896His
ENST00000426933.6:c.191C>A	ENSP00000413345.2:p.Pro64His
ENST00000526579.5:n.178-982C>A
ENST00000527116.5:n.449C>A
ENST00000528555.5:c.827C>A	ENSP00000435122.1:p.Pro276His
ENST00000530330.1:n.423C>A
ENST00000530356.5:c.827C>A	ENSP00000432307.1:p.Pro276His
ENST00000533318.5:n.1047C>A
ENST00000534726.5:c.407C>A	ENSP00000433699.1:p.Pro136His
NM_001301089.1:c.827C>A	NP_001288018.1:p.Pro276His
NM_014758.2:c.2687C>A	NP_055573.2:p.Pro896His
XM_005271546.3:c.2574-982C>A	XP_005271603.1:n.2574-982C>A
XM_011542819.1:c.2933C>A	XP_011541121.1:p.Pro978His
XM_011542820.1:c.2921C>A	XP_011541122.1:p.Pro974His
XM_011542821.1:c.2813C>A	XP_011541123.1:p.Pro938His
XM_011542824.1:c.2051C>A	XP_011541126.1:p.Pro684His
XM_011542825.1:c.1208C>A	XP_011541127.1:p.Pro403His
XM_011542826.1:c.1073C>A	XP_011541128.1:p.Pro358His
XM_011542827.1:c.953C>A	XP_011541129.1:p.Pro318His
NM_001347918.1:c.2567C>A	NP_001334847.1:p.Pro856His
NM_001347919.1:c.2574-982C>A	NP_001334848.1:n.2574-982C>A
NM_001347922.1:c.1016C>A	NP_001334851.1:p.Pro339His
NM_001347923.1:c.962C>A	NP_001334852.1:p.Pro321His
NM_001347924.1:c.707C>A	NP_001334853.1:p.Pro236His
NM_001347925.1:c.653C>A	NP_001334854.1:p.Pro218His
NM_001347926.1:c.714-982C>A	NP_001334855.1:n.714-982C>A
NM_001347927.1:c.407C>A	NP_001334856.1:p.Pro136His
NR_144939.1:n.3320C>A
XM_011542820.2:c.2921C>A	XP_011541122.1:p.Pro974His
XM_011542821.3:c.2813C>A	XP_011541123.1:p.Pro938His
XM_011542824.2:c.2051C>A	XP_011541126.1:p.Pro684His
XM_011542825.2:c.1208C>A	XP_011541127.1:p.Pro403His
XM_011542826.2:c.1073C>A	XP_011541128.1:p.Pro358His
XM_024448521.1:c.2933C>A	XP_024304289.1:p.Pro978His
XR_001747870.1:n.3758C>A
XR_001747872.1:n.3104C>A
XR_001747873.1:n.3418C>A
NM_001301089.2:c.827C>A	NP_001288018.1:p.Pro276His
NM_001347918.2:c.2567C>A	NP_001334847.2:p.Pro856His
NM_001347919.2:c.2574-982C>A	NP_001334848.2:n.2574-982C>A
NM_001347920.2:c.*21083C>A	NP_001334849.2:n.*21083C>A
NM_001347922.2:c.1016C>A	NP_001334851.2:p.Pro339His
NM_001347923.2:c.962C>A	NP_001334852.2:p.Pro321His
NM_001347924.2:c.707C>A	NP_001334853.1:p.Pro236His
NM_001347925.2:c.653C>A	NP_001334854.1:p.Pro218His
NM_001347926.2:c.714-982C>A	NP_001334855.1:n.714-982C>A
NM_001347927.2:c.407C>A	NP_001334856.1:p.Pro136His
NM_014758.3:c.2687C>A MANE Select	NP_055573.3:p.Pro896His
NR_144939.2:n.3312C>A