Canonical Allele Identifier: CA2658341418

Gene: SNX17

Linked Data

• gnomAD v4: 2-27375230-T-TCTCTGTCTTCCTCTAAGGGCTTG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375231_27375232insTCTGTCTTCCTCTAAGGGCTTGC , CM000664.2:g.27375231_27375232insTCTGTCTTCCTCTAAGGGCTTGC	GRCh38
NC_000002.11:g.27598098_27598099insTCTGTCTTCCTCTAAGGGCTTGC , CM000664.1:g.27598098_27598099insTCTGTCTTCCTCTAAGGGCTTGC	GRCh37
NC_000002.10:g.27451602_27451603insTCTGTCTTCCTCTAAGGGCTTGC	NCBI36
NG_009305.1:g.227_228insCAAGCCCTTAGAGGAAGACAGAG
NG_028219.1:g.10514_10515insCAAGCCCTTAGAGGAAGACAGAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000233575.7:c.774+78_774+79insTCTGTCTTCCTCTAAGGGCTTGC MANE Select	ENSP00000233575.2:n.774+78_774+79insTCTGT...
ENST00000233575.6:c.774+78_774+79insTCTGTCTTCCTCTAAGGGCTTGC	ENSP00000233575.2:n.774+78_774+79insTCTGT...
ENST00000427123.5:c.*584+78_*584+79insTCTGTCTTCCTCTAAGGGCTTGC	ENSP00000405399.1:n.*584+78_*584+79insTCT...
ENST00000440760.5:c.*619+78_*619+79insTCTGTCTTCCTCTAAGGGCTTGC	ENSP00000399727.1:n.*619+78_*619+79insTCT...
ENST00000453453.1:c.*301+78_*301+79insTCTGTCTTCCTCTAAGGGCTTGC	ENSP00000401922.1:n.*301+78_*301+79insTCT...
ENST00000493711.1:n.491+78_491+79insTCTGTCTTCCTCTAAGGGCTTGC
ENST00000494893.5:n.950+78_950+79insTCTGTCTTCCTCTAAGGGCTTGC
ENST00000537606.5:c.699+78_699+79insTCTGTCTTCCTCTAAGGGCTTGC	ENSP00000439208.1:n.699+78_699+79insTCTGT...
NM_001267059.1:c.738+78_738+79insTCTGTCTTCCTCTAAGGGCTTGC	NP_001253988.1:n.738+78_738+79insTCTGTCTT...
NM_001267060.1:c.699+78_699+79insTCTGTCTTCCTCTAAGGGCTTGC	NP_001253989.1:n.699+78_699+79insTCTGTCTT...
NM_001267061.1:c.714+78_714+79insTCTGTCTTCCTCTAAGGGCTTGC	NP_001253990.1:n.714+78_714+79insTCTGTCTT...
NM_014748.3:c.774+78_774+79insTCTGTCTTCCTCTAAGGGCTTGC	NP_055563.1:n.774+78_774+79insTCTGTCTTCCT...
NR_049782.1:n.1147+78_1147+79insTCTGTCTTCCTCTAAGGGCTTGC
NR_049783.1:n.1120+78_1120+79insTCTGTCTTCCTCTAAGGGCTTGC
NR_049784.1:n.1096+78_1096+79insTCTGTCTTCCTCTAAGGGCTTGC
NR_049785.1:n.1029+78_1029+79insTCTGTCTTCCTCTAAGGGCTTGC
NR_049786.1:n.978+78_978+79insTCTGTCTTCCTCTAAGGGCTTGC
NR_049787.1:n.829+78_829+79insTCTGTCTTCCTCTAAGGGCTTGC
NR_049788.1:n.759+78_759+79insTCTGTCTTCCTCTAAGGGCTTGC
XM_011533203.1:c.132+78_132+79insTCTGTCTTCCTCTAAGGGCTTGC	XP_011531505.1:n.132+78_132+79insTCTGTCTT...
XM_011533203.2:c.132+78_132+79insTCTGTCTTCCTCTAAGGGCTTGC	XP_011531505.1:n.132+78_132+79insTCTGTCTT...
XM_017005405.2:c.132+78_132+79insTCTGTCTTCCTCTAAGGGCTTGC	XP_016860894.1:n.132+78_132+79insTCTGTCTT...
NM_014748.4:c.774+78_774+79insTCTGTCTTCCTCTAAGGGCTTGC MANE Select	NP_055563.1:n.774+78_774+79insTCTGTCTTCCT...
NM_001267059.2:c.738+78_738+79insTCTGTCTTCCTCTAAGGGCTTGC	NP_001253988.1:n.738+78_738+79insTCTGTCTT...
NM_001267061.2:c.714+78_714+79insTCTGTCTTCCTCTAAGGGCTTGC	NP_001253990.1:n.714+78_714+79insTCTGTCTT...
NR_049782.2:n.1027+78_1027+79insTCTGTCTTCCTCTAAGGGCTTGC
NR_049783.2:n.1000+78_1000+79insTCTGTCTTCCTCTAAGGGCTTGC
NR_049784.2:n.976+78_976+79insTCTGTCTTCCTCTAAGGGCTTGC
NR_049785.2:n.909+78_909+79insTCTGTCTTCCTCTAAGGGCTTGC
NR_049786.2:n.858+78_858+79insTCTGTCTTCCTCTAAGGGCTTGC
NR_049787.2:n.709+78_709+79insTCTGTCTTCCTCTAAGGGCTTGC
NR_049788.2:n.639+78_639+79insTCTGTCTTCCTCTAAGGGCTTGC
NM_001267060.2:c.699+78_699+79insTCTGTCTTCCTCTAAGGGCTTGC	NP_001253989.1:n.699+78_699+79insTCTGTCTT...