Canonical Allele Identifier: CA2658341642

Gene: SNX17

Linked Data

• gnomAD v4: 2-27375374-G-GAGCTCC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375374_27375375insAGCTCC , CM000664.2:g.27375374_27375375insAGCTCC	GRCh38
NC_000002.11:g.27598241_27598242insAGCTCC , CM000664.1:g.27598241_27598242insAGCTCC	GRCh37
NC_000002.10:g.27451745_27451746insAGCTCC	NCBI36
NG_009305.1:g.83_84insGGAGCT
NG_028219.1:g.10370_10371insGGAGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.775-132_775-131insAGCTCC MANE Select	ENSP00000233575.2:n.775-132_775-131insAGCTCC
ENST00000233575.6:c.775-132_775-131insAGCTCC	ENSP00000233575.2:n.775-132_775-131insAGCTCC
ENST00000427123.5:c.*585-132_*585-131insAGCTCC	ENSP00000405399.1:n.*585-132_*585-131insAGCTCC
ENST00000440760.5:c.*620-132_*620-131insAGCTCC	ENSP00000399727.1:n.*620-132_*620-131insAGCTCC
ENST00000453453.1:c.*302-132_*302-131insAGCTCC	ENSP00000401922.1:n.*302-132_*302-131insAGCTCC
ENST00000493711.1:n.492-132_492-131insAGCTCC
ENST00000494893.5:n.951-132_951-131insAGCTCC
ENST00000537606.5:c.700-132_700-131insAGCTCC	ENSP00000439208.1:n.700-132_700-131insAGCTCC
NM_001267059.1:c.739-132_739-131insAGCTCC	NP_001253988.1:n.739-132_739-131insAGCTCC
NM_001267060.1:c.700-132_700-131insAGCTCC	NP_001253989.1:n.700-132_700-131insAGCTCC
NM_001267061.1:c.715-132_715-131insAGCTCC	NP_001253990.1:n.715-132_715-131insAGCTCC
NM_014748.3:c.775-132_775-131insAGCTCC	NP_055563.1:n.775-132_775-131insAGCTCC
NR_049782.1:n.1148-132_1148-131insAGCTCC
NR_049783.1:n.1121-132_1121-131insAGCTCC
NR_049784.1:n.1097-132_1097-131insAGCTCC
NR_049785.1:n.1030-132_1030-131insAGCTCC
NR_049786.1:n.979-132_979-131insAGCTCC
NR_049787.1:n.830-132_830-131insAGCTCC
NR_049788.1:n.760-132_760-131insAGCTCC
XM_011533203.1:c.133-132_133-131insAGCTCC	XP_011531505.1:n.133-132_133-131insAGCTCC
XM_011533203.2:c.133-132_133-131insAGCTCC	XP_011531505.1:n.133-132_133-131insAGCTCC
XM_017005405.2:c.133-132_133-131insAGCTCC	XP_016860894.1:n.133-132_133-131insAGCTCC
NM_014748.4:c.775-132_775-131insAGCTCC MANE Select	NP_055563.1:n.775-132_775-131insAGCTCC
NM_001267059.2:c.739-132_739-131insAGCTCC	NP_001253988.1:n.739-132_739-131insAGCTCC
NM_001267061.2:c.715-132_715-131insAGCTCC	NP_001253990.1:n.715-132_715-131insAGCTCC
NR_049782.2:n.1028-132_1028-131insAGCTCC
NR_049783.2:n.1001-132_1001-131insAGCTCC
NR_049784.2:n.977-132_977-131insAGCTCC
NR_049785.2:n.910-132_910-131insAGCTCC
NR_049786.2:n.859-132_859-131insAGCTCC
NR_049787.2:n.710-132_710-131insAGCTCC
NR_049788.2:n.640-132_640-131insAGCTCC
NM_001267060.2:c.700-132_700-131insAGCTCC	NP_001253989.1:n.700-132_700-131insAGCTCC