Canonical Allele Identifier: CA383457909

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750677A>C (hg19) ; chr11:g.130880782A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880782A>C , CM000673.2:g.130880782A>C	GRCh38
NC_000011.9:g.130750677A>C , CM000673.1:g.130750677A>C	GRCh37
NC_000011.8:g.130255887A>C	NCBI36
NG_053190.1:g.40707T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2598T>G MANE Select	ENSP00000265909.4:p.Asn866Lys
ENST00000265909.8:c.2598T>G	ENSP00000265909.4:p.Asn866Lys
ENST00000426933.6:c.102T>G	ENSP00000413345.2:p.Asn34Lys
ENST00000526579.5:n.178-1071T>G
ENST00000527116.5:n.360T>G
ENST00000528555.5:c.738T>G	ENSP00000435122.1:p.Asn246Lys
ENST00000530330.1:n.334T>G
ENST00000530356.5:c.738T>G	ENSP00000432307.1:p.Asn246Lys
ENST00000533318.5:n.958T>G
ENST00000534726.5:c.318T>G	ENSP00000433699.1:p.Asn106Lys
NM_001301089.1:c.738T>G	NP_001288018.1:p.Asn246Lys
NM_014758.2:c.2598T>G	NP_055573.2:p.Asn866Lys
XM_005271546.3:c.2574-1071T>G	XP_005271603.1:n.2574-1071T>G
XM_011542819.1:c.2844T>G	XP_011541121.1:p.Asn948Lys
XM_011542820.1:c.2832T>G	XP_011541122.1:p.Asn944Lys
XM_011542821.1:c.2724T>G	XP_011541123.1:p.Asn908Lys
XM_011542824.1:c.1962T>G	XP_011541126.1:p.Asn654Lys
XM_011542825.1:c.1119T>G	XP_011541127.1:p.Asn373Lys
XM_011542826.1:c.984T>G	XP_011541128.1:p.Asn328Lys
XM_011542827.1:c.864T>G	XP_011541129.1:p.Asn288Lys
NM_001347918.1:c.2478T>G	NP_001334847.1:p.Asn826Lys
NM_001347919.1:c.2574-1071T>G	NP_001334848.1:n.2574-1071T>G
NM_001347922.1:c.927T>G	NP_001334851.1:p.Asn309Lys
NM_001347923.1:c.873T>G	NP_001334852.1:p.Asn291Lys
NM_001347924.1:c.618T>G	NP_001334853.1:p.Asn206Lys
NM_001347925.1:c.564T>G	NP_001334854.1:p.Asn188Lys
NM_001347926.1:c.714-1071T>G	NP_001334855.1:n.714-1071T>G
NM_001347927.1:c.318T>G	NP_001334856.1:p.Asn106Lys
NR_144939.1:n.3231T>G
XM_011542820.2:c.2832T>G	XP_011541122.1:p.Asn944Lys
XM_011542821.3:c.2724T>G	XP_011541123.1:p.Asn908Lys
XM_011542824.2:c.1962T>G	XP_011541126.1:p.Asn654Lys
XM_011542825.2:c.1119T>G	XP_011541127.1:p.Asn373Lys
XM_011542826.2:c.984T>G	XP_011541128.1:p.Asn328Lys
XM_024448521.1:c.2844T>G	XP_024304289.1:p.Asn948Lys
XR_001747870.1:n.3669T>G
XR_001747872.1:n.3015T>G
XR_001747873.1:n.3329T>G
NM_001301089.2:c.738T>G	NP_001288018.1:p.Asn246Lys
NM_001347918.2:c.2478T>G	NP_001334847.2:p.Asn826Lys
NM_001347919.2:c.2574-1071T>G	NP_001334848.2:n.2574-1071T>G
NM_001347920.2:c.*20994T>G	NP_001334849.2:n.*20994T>G
NM_001347922.2:c.927T>G	NP_001334851.2:p.Asn309Lys
NM_001347923.2:c.873T>G	NP_001334852.2:p.Asn291Lys
NM_001347924.2:c.618T>G	NP_001334853.1:p.Asn206Lys
NM_001347925.2:c.564T>G	NP_001334854.1:p.Asn188Lys
NM_001347926.2:c.714-1071T>G	NP_001334855.1:n.714-1071T>G
NM_001347927.2:c.318T>G	NP_001334856.1:p.Asn106Lys
NM_014758.3:c.2598T>G MANE Select	NP_055573.3:p.Asn866Lys
NR_144939.2:n.3223T>G