Canonical Allele Identifier: CA1240248005

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375092T= , CM000664.2:g.27375092T=	GRCh38
NC_000002.11:g.27597959T= , CM000664.1:g.27597959T=	GRCh37
NC_000002.10:g.27451463T=	NCBI36
NG_009305.1:g.366A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.713T= MANE Select	ENSP00000233575.2:p.Leu238=
ENST00000233575.6:c.713T=	ENSP00000233575.2:p.Leu238=
ENST00000427123.5:c.*523T=	ENSP00000405399.1:n.*523T=
ENST00000440760.5:c.*558T=	ENSP00000399727.1:n.*558T=
ENST00000453453.1:c.*240T=	ENSP00000401922.1:n.*240T=
ENST00000493711.1:n.430T=
ENST00000494893.5:n.889T=
ENST00000537606.5:c.638T=	ENSP00000439208.1:p.Leu213=
NM_001267059.1:c.677T=	NP_001253988.1:p.Leu226=
NM_001267060.1:c.638T=	NP_001253989.1:p.Leu213=
NM_001267061.1:c.653T=	NP_001253990.1:p.Leu218=
NM_014748.3:c.713T=	NP_055563.1:p.Leu238=
NR_049782.1:n.1086T=
NR_049783.1:n.1059T=
NR_049784.1:n.1035T=
NR_049785.1:n.968T=
NR_049786.1:n.917T=
NR_049787.1:n.768T=
NR_049788.1:n.698T=
XM_011533203.1:c.71T=	XP_011531505.1:p.Leu24=
XM_011533203.2:c.71T=	XP_011531505.1:p.Leu24=
XM_017005405.2:c.71T=	XP_016860894.1:p.Leu24=
NM_014748.4:c.713T= MANE Select	NP_055563.1:p.Leu238=
NM_001267059.2:c.677T=	NP_001253988.1:p.Leu226=
NM_001267061.2:c.653T=	NP_001253990.1:p.Leu218=
NR_049782.2:n.966T=
NR_049783.2:n.939T=
NR_049784.2:n.915T=
NR_049785.2:n.848T=
NR_049786.2:n.797T=
NR_049787.2:n.648T=
NR_049788.2:n.578T=
NM_001267060.2:c.638T=	NP_001253989.1:p.Leu213=