Canonical Allele Identifier: CA2658341364

Gene: SNX17

Linked Data

• gnomAD v4: 2-27375155-TGAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375156_27375158del , CM000664.2:g.27375156_27375158del	GRCh38
NC_000002.11:g.27598023_27598025del , CM000664.1:g.27598023_27598025del	GRCh37
NC_000002.10:g.27451527_27451529del	NCBI36
NG_009305.1:g.300_302del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.774+3_774+5del MANE Select	ENSP00000233575.2:n.774+3_774+5del
ENST00000233575.6:c.774+3_774+5del	ENSP00000233575.2:n.774+3_774+5del
ENST00000427123.5:c.*584+3_*584+5del	ENSP00000405399.1:n.*584+3_*584+5del
ENST00000440760.5:c.*619+3_*619+5del	ENSP00000399727.1:n.*619+3_*619+5del
ENST00000453453.1:c.*301+3_*301+5del	ENSP00000401922.1:n.*301+3_*301+5del
ENST00000493711.1:n.491+3_491+5del
ENST00000494893.5:n.950+3_950+5del
ENST00000537606.5:c.699+3_699+5del	ENSP00000439208.1:n.699+3_699+5del
NM_001267059.1:c.738+3_738+5del	NP_001253988.1:n.738+3_738+5del
NM_001267060.1:c.699+3_699+5del	NP_001253989.1:n.699+3_699+5del
NM_001267061.1:c.714+3_714+5del	NP_001253990.1:n.714+3_714+5del
NM_014748.3:c.774+3_774+5del	NP_055563.1:n.774+3_774+5del
NR_049782.1:n.1147+3_1147+5del
NR_049783.1:n.1120+3_1120+5del
NR_049784.1:n.1096+3_1096+5del
NR_049785.1:n.1029+3_1029+5del
NR_049786.1:n.978+3_978+5del
NR_049787.1:n.829+3_829+5del
NR_049788.1:n.759+3_759+5del
XM_011533203.1:c.132+3_132+5del	XP_011531505.1:n.132+3_132+5del
XM_011533203.2:c.132+3_132+5del	XP_011531505.1:n.132+3_132+5del
XM_017005405.2:c.132+3_132+5del	XP_016860894.1:n.132+3_132+5del
NM_014748.4:c.774+3_774+5del MANE Select	NP_055563.1:n.774+3_774+5del
NM_001267059.2:c.738+3_738+5del	NP_001253988.1:n.738+3_738+5del
NM_001267061.2:c.714+3_714+5del	NP_001253990.1:n.714+3_714+5del
NR_049782.2:n.1027+3_1027+5del
NR_049783.2:n.1000+3_1000+5del
NR_049784.2:n.976+3_976+5del
NR_049785.2:n.909+3_909+5del
NR_049786.2:n.858+3_858+5del
NR_049787.2:n.709+3_709+5del
NR_049788.2:n.639+3_639+5del
NM_001267060.2:c.699+3_699+5del	NP_001253989.1:n.699+3_699+5del