Canonical Allele Identifier: CA1240248801

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375551T= , CM000664.2:g.27375551T=	GRCh38
NC_000002.11:g.27598418T= , CM000664.1:g.27598418T=	GRCh37
NC_000002.10:g.27451922T=	NCBI36
NG_028219.1:g.10194A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.820T= MANE Select	ENSP00000233575.2:p.Phe274=
ENST00000233575.6:c.820T=	ENSP00000233575.2:p.Phe274=
ENST00000427123.5:c.*630T=	ENSP00000405399.1:n.*630T=
ENST00000440760.5:c.*665T=	ENSP00000399727.1:n.*665T=
ENST00000453453.1:c.*347T=	ENSP00000401922.1:n.*347T=
ENST00000493711.1:n.537T=
ENST00000537606.5:c.745T=	ENSP00000439208.1:p.Phe249=
NM_001267059.1:c.784T=	NP_001253988.1:p.Phe262=
NM_001267060.1:c.745T=	NP_001253989.1:p.Phe249=
NM_001267061.1:c.760T=	NP_001253990.1:p.Phe254=
NM_014748.3:c.820T=	NP_055563.1:p.Phe274=
NR_049782.1:n.1193T=
NR_049783.1:n.1166T=
NR_049784.1:n.1142T=
NR_049785.1:n.1075T=
NR_049786.1:n.1024T=
NR_049787.1:n.875T=
NR_049788.1:n.805T=
XM_011533203.1:c.178T=	XP_011531505.1:p.Phe60=
XM_011533203.2:c.178T=	XP_011531505.1:p.Phe60=
XM_017005405.2:c.178T=	XP_016860894.1:p.Phe60=
NM_014748.4:c.820T= MANE Select	NP_055563.1:p.Phe274=
NM_001267059.2:c.784T=	NP_001253988.1:p.Phe262=
NM_001267061.2:c.760T=	NP_001253990.1:p.Phe254=
NR_049782.2:n.1073T=
NR_049783.2:n.1046T=
NR_049784.2:n.1022T=
NR_049785.2:n.955T=
NR_049786.2:n.904T=
NR_049787.2:n.755T=
NR_049788.2:n.685T=
NM_001267060.2:c.745T=	NP_001253989.1:p.Phe249=