Canonical Allele Identifier: CA1240248441

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375393_27375401delinsCTCCTAAAG , CM000664.2:g.27375393_27375401delinsCTCCTAAAG	GRCh38
NC_000002.11:g.27598260_27598268delinsCTCCTAAAG , CM000664.1:g.27598260_27598268delinsCTCCTAAAG	GRCh37
NC_000002.10:g.27451764_27451772delinsCTCCTAAAG	NCBI36
NG_009305.1:g.57_65delinsCTTTAGGAG
NG_028219.1:g.10344_10352delinsCTTTAGGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.775-113_775-105delinsCTCCTAAAG MANE Select	ENSP00000233575.2:n.775-113_775-105delinsCTCCTAAAG
ENST00000233575.6:c.775-113_775-105delinsCTCCTAAAG	ENSP00000233575.2:n.775-113_775-105delinsCTCCTAAAG
ENST00000427123.5:c.*585-113_*585-105delinsCTCCTAAAG	ENSP00000405399.1:n.*585-113_*585-105delinsCTCCTAAAG
ENST00000440760.5:c.*620-113_*620-105delinsCTCCTAAAG	ENSP00000399727.1:n.*620-113_*620-105delinsCTCCTAAAG
ENST00000453453.1:c.*302-113_*302-105delinsCTCCTAAAG	ENSP00000401922.1:n.*302-113_*302-105delinsCTCCTAAAG
ENST00000493711.1:n.492-113_492-105delinsCTCCTAAAG
ENST00000494893.5:n.951-113_951-105delinsCTCCTAAAG
ENST00000537606.5:c.700-113_700-105delinsCTCCTAAAG	ENSP00000439208.1:n.700-113_700-105delinsCTCCTAAAG
NM_001267059.1:c.739-113_739-105delinsCTCCTAAAG	NP_001253988.1:n.739-113_739-105delinsCTCCTAAAG
NM_001267060.1:c.700-113_700-105delinsCTCCTAAAG	NP_001253989.1:n.700-113_700-105delinsCTCCTAAAG
NM_001267061.1:c.715-113_715-105delinsCTCCTAAAG	NP_001253990.1:n.715-113_715-105delinsCTCCTAAAG
NM_014748.3:c.775-113_775-105delinsCTCCTAAAG	NP_055563.1:n.775-113_775-105delinsCTCCTAAAG
NR_049782.1:n.1148-113_1148-105delinsCTCCTAAAG
NR_049783.1:n.1121-113_1121-105delinsCTCCTAAAG
NR_049784.1:n.1097-113_1097-105delinsCTCCTAAAG
NR_049785.1:n.1030-113_1030-105delinsCTCCTAAAG
NR_049786.1:n.979-113_979-105delinsCTCCTAAAG
NR_049787.1:n.830-113_830-105delinsCTCCTAAAG
NR_049788.1:n.760-113_760-105delinsCTCCTAAAG
XM_011533203.1:c.133-113_133-105delinsCTCCTAAAG	XP_011531505.1:n.133-113_133-105delinsCTCCTAAAG
XM_011533203.2:c.133-113_133-105delinsCTCCTAAAG	XP_011531505.1:n.133-113_133-105delinsCTCCTAAAG
XM_017005405.2:c.133-113_133-105delinsCTCCTAAAG	XP_016860894.1:n.133-113_133-105delinsCTCCTAAAG
NM_014748.4:c.775-113_775-105delinsCTCCTAAAG MANE Select	NP_055563.1:n.775-113_775-105delinsCTCCTAAAG
NM_001267059.2:c.739-113_739-105delinsCTCCTAAAG	NP_001253988.1:n.739-113_739-105delinsCTCCTAAAG
NM_001267061.2:c.715-113_715-105delinsCTCCTAAAG	NP_001253990.1:n.715-113_715-105delinsCTCCTAAAG
NR_049782.2:n.1028-113_1028-105delinsCTCCTAAAG
NR_049783.2:n.1001-113_1001-105delinsCTCCTAAAG
NR_049784.2:n.977-113_977-105delinsCTCCTAAAG
NR_049785.2:n.910-113_910-105delinsCTCCTAAAG
NR_049786.2:n.859-113_859-105delinsCTCCTAAAG
NR_049787.2:n.710-113_710-105delinsCTCCTAAAG
NR_049788.2:n.640-113_640-105delinsCTCCTAAAG
NM_001267060.2:c.700-113_700-105delinsCTCCTAAAG	NP_001253989.1:n.700-113_700-105delinsCTCCTAAAG