Canonical Allele Identifier: CA383457614

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750537C>G (hg19) ; chr11:g.130880642C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880642C>G , CM000673.2:g.130880642C>G	GRCh38
NC_000011.9:g.130750537C>G , CM000673.1:g.130750537C>G	GRCh37
NC_000011.8:g.130255747C>G	NCBI36
NG_053190.1:g.40847G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2738G>C MANE Select	ENSP00000265909.4:p.Ser913Thr
ENST00000265909.8:c.2738G>C	ENSP00000265909.4:p.Ser913Thr
ENST00000426933.6:c.242G>C	ENSP00000413345.2:p.Ser81Thr
ENST00000526579.5:n.178-931G>C
ENST00000527116.5:n.500G>C
ENST00000528555.5:c.878G>C	ENSP00000435122.1:p.Ser293Thr
ENST00000530330.1:n.474G>C
ENST00000530356.5:c.878G>C	ENSP00000432307.1:p.Ser293Thr
ENST00000533318.5:n.1098G>C
ENST00000534726.5:c.458G>C	ENSP00000433699.1:p.Ser153Thr
NM_001301089.1:c.878G>C	NP_001288018.1:p.Ser293Thr
NM_014758.2:c.2738G>C	NP_055573.2:p.Ser913Thr
XM_005271546.3:c.2574-931G>C	XP_005271603.1:n.2574-931G>C
XM_011542819.1:c.2984G>C	XP_011541121.1:p.Ser995Thr
XM_011542820.1:c.2972G>C	XP_011541122.1:p.Ser991Thr
XM_011542821.1:c.2864G>C	XP_011541123.1:p.Ser955Thr
XM_011542824.1:c.2102G>C	XP_011541126.1:p.Ser701Thr
XM_011542825.1:c.1259G>C	XP_011541127.1:p.Ser420Thr
XM_011542826.1:c.1124G>C	XP_011541128.1:p.Ser375Thr
XM_011542827.1:c.1004G>C	XP_011541129.1:p.Ser335Thr
NM_001347918.1:c.2618G>C	NP_001334847.1:p.Ser873Thr
NM_001347919.1:c.2574-931G>C	NP_001334848.1:n.2574-931G>C
NM_001347922.1:c.1067G>C	NP_001334851.1:p.Ser356Thr
NM_001347923.1:c.1013G>C	NP_001334852.1:p.Ser338Thr
NM_001347924.1:c.758G>C	NP_001334853.1:p.Ser253Thr
NM_001347925.1:c.704G>C	NP_001334854.1:p.Ser235Thr
NM_001347926.1:c.714-931G>C	NP_001334855.1:n.714-931G>C
NM_001347927.1:c.458G>C	NP_001334856.1:p.Ser153Thr
NR_144939.1:n.3371G>C
XM_011542820.2:c.2972G>C	XP_011541122.1:p.Ser991Thr
XM_011542821.3:c.2864G>C	XP_011541123.1:p.Ser955Thr
XM_011542824.2:c.2102G>C	XP_011541126.1:p.Ser701Thr
XM_011542825.2:c.1259G>C	XP_011541127.1:p.Ser420Thr
XM_011542826.2:c.1124G>C	XP_011541128.1:p.Ser375Thr
XM_024448521.1:c.2984G>C	XP_024304289.1:p.Ser995Thr
XR_001747870.1:n.3809G>C
XR_001747872.1:n.3155G>C
XR_001747873.1:n.3469G>C
NM_001301089.2:c.878G>C	NP_001288018.1:p.Ser293Thr
NM_001347918.2:c.2618G>C	NP_001334847.2:p.Ser873Thr
NM_001347919.2:c.2574-931G>C	NP_001334848.2:n.2574-931G>C
NM_001347920.2:c.*21134G>C	NP_001334849.2:n.*21134G>C
NM_001347922.2:c.1067G>C	NP_001334851.2:p.Ser356Thr
NM_001347923.2:c.1013G>C	NP_001334852.2:p.Ser338Thr
NM_001347924.2:c.758G>C	NP_001334853.1:p.Ser253Thr
NM_001347925.2:c.704G>C	NP_001334854.1:p.Ser235Thr
NM_001347926.2:c.714-931G>C	NP_001334855.1:n.714-931G>C
NM_001347927.2:c.458G>C	NP_001334856.1:p.Ser153Thr
NM_014758.3:c.2738G>C MANE Select	NP_055573.3:p.Ser913Thr
NR_144939.2:n.3363G>C