Canonical Allele Identifier: CA2567296043

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375232A>G , CM000664.2:g.27375232A>G	GRCh38
NC_000002.11:g.27598099A>G , CM000664.1:g.27598099A>G	GRCh37
NC_000002.10:g.27451603A>G	NCBI36
NG_009305.1:g.226T>C
NG_028219.1:g.10513T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000233575.7:c.774+79A>G MANE Select	ENSP00000233575.2:n.774+79A>G
ENST00000233575.6:c.774+79A>G	ENSP00000233575.2:n.774+79A>G
ENST00000427123.5:c.*584+79A>G	ENSP00000405399.1:n.*584+79A>G
ENST00000440760.5:c.*619+79A>G	ENSP00000399727.1:n.*619+79A>G
ENST00000453453.1:c.*301+79A>G	ENSP00000401922.1:n.*301+79A>G
ENST00000493711.1:n.491+79A>G
ENST00000494893.5:n.950+79A>G
ENST00000537606.5:c.699+79A>G	ENSP00000439208.1:n.699+79A>G
NM_001267059.1:c.738+79A>G	NP_001253988.1:n.738+79A>G
NM_001267060.1:c.699+79A>G	NP_001253989.1:n.699+79A>G
NM_001267061.1:c.714+79A>G	NP_001253990.1:n.714+79A>G
NM_014748.3:c.774+79A>G	NP_055563.1:n.774+79A>G
NR_049782.1:n.1147+79A>G
NR_049783.1:n.1120+79A>G
NR_049784.1:n.1096+79A>G
NR_049785.1:n.1029+79A>G
NR_049786.1:n.978+79A>G
NR_049787.1:n.829+79A>G
NR_049788.1:n.759+79A>G
XM_011533203.1:c.132+79A>G	XP_011531505.1:n.132+79A>G
XM_011533203.2:c.132+79A>G	XP_011531505.1:n.132+79A>G
XM_017005405.2:c.132+79A>G	XP_016860894.1:n.132+79A>G
NM_014748.4:c.774+79A>G MANE Select	NP_055563.1:n.774+79A>G
NM_001267059.2:c.738+79A>G	NP_001253988.1:n.738+79A>G
NM_001267061.2:c.714+79A>G	NP_001253990.1:n.714+79A>G
NR_049782.2:n.1027+79A>G
NR_049783.2:n.1000+79A>G
NR_049784.2:n.976+79A>G
NR_049785.2:n.909+79A>G
NR_049786.2:n.858+79A>G
NR_049787.2:n.709+79A>G
NR_049788.2:n.639+79A>G
NM_001267060.2:c.699+79A>G	NP_001253989.1:n.699+79A>G