Canonical Allele Identifier: CA1240248654

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375506T= , CM000664.2:g.27375506T=	GRCh38
NC_000002.11:g.27598373T= , CM000664.1:g.27598373T=	GRCh37
NC_000002.10:g.27451877T=	NCBI36
NG_028219.1:g.10239A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.775T= MANE Select	ENSP00000233575.2:p.Phe259=
ENST00000233575.6:c.775T=	ENSP00000233575.2:p.Phe259=
ENST00000427123.5:c.*585T=	ENSP00000405399.1:n.*585T=
ENST00000440760.5:c.*620T=	ENSP00000399727.1:n.*620T=
ENST00000453453.1:c.*302T=	ENSP00000401922.1:n.*302T=
ENST00000493711.1:n.492T=
ENST00000494893.5:n.951T=
ENST00000537606.5:c.700T=	ENSP00000439208.1:p.Phe234=
NM_001267059.1:c.739T=	NP_001253988.1:p.Phe247=
NM_001267060.1:c.700T=	NP_001253989.1:p.Phe234=
NM_001267061.1:c.715T=	NP_001253990.1:p.Phe239=
NM_014748.3:c.775T=	NP_055563.1:p.Phe259=
NR_049782.1:n.1148T=
NR_049783.1:n.1121T=
NR_049784.1:n.1097T=
NR_049785.1:n.1030T=
NR_049786.1:n.979T=
NR_049787.1:n.830T=
NR_049788.1:n.760T=
XM_011533203.1:c.133T=	XP_011531505.1:p.Phe45=
XM_011533203.2:c.133T=	XP_011531505.1:p.Phe45=
XM_017005405.2:c.133T=	XP_016860894.1:p.Phe45=
NM_014748.4:c.775T= MANE Select	NP_055563.1:p.Phe259=
NM_001267059.2:c.739T=	NP_001253988.1:p.Phe247=
NM_001267061.2:c.715T=	NP_001253990.1:p.Phe239=
NR_049782.2:n.1028T=
NR_049783.2:n.1001T=
NR_049784.2:n.977T=
NR_049785.2:n.910T=
NR_049786.2:n.859T=
NR_049787.2:n.710T=
NR_049788.2:n.640T=
NM_001267060.2:c.700T=	NP_001253989.1:p.Phe234=