Canonical Allele Identifier: CA1240248087

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375179C= , CM000664.2:g.27375179C=	GRCh38
NC_000002.11:g.27598046C= , CM000664.1:g.27598046C=	GRCh37
NC_000002.10:g.27451550C=	NCBI36
NG_009305.1:g.279G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.774+26C= MANE Select	ENSP00000233575.2:n.774+26C=
ENST00000233575.6:c.774+26C=	ENSP00000233575.2:n.774+26C=
ENST00000427123.5:c.*584+26C=	ENSP00000405399.1:n.*584+26C=
ENST00000440760.5:c.*619+26C=	ENSP00000399727.1:n.*619+26C=
ENST00000453453.1:c.*301+26C=	ENSP00000401922.1:n.*301+26C=
ENST00000493711.1:n.491+26C=
ENST00000494893.5:n.950+26C=
ENST00000537606.5:c.699+26C=	ENSP00000439208.1:n.699+26C=
NM_001267059.1:c.738+26C=	NP_001253988.1:n.738+26C=
NM_001267060.1:c.699+26C=	NP_001253989.1:n.699+26C=
NM_001267061.1:c.714+26C=	NP_001253990.1:n.714+26C=
NM_014748.3:c.774+26C=	NP_055563.1:n.774+26C=
NR_049782.1:n.1147+26C=
NR_049783.1:n.1120+26C=
NR_049784.1:n.1096+26C=
NR_049785.1:n.1029+26C=
NR_049786.1:n.978+26C=
NR_049787.1:n.829+26C=
NR_049788.1:n.759+26C=
XM_011533203.1:c.132+26C=	XP_011531505.1:n.132+26C=
XM_011533203.2:c.132+26C=	XP_011531505.1:n.132+26C=
XM_017005405.2:c.132+26C=	XP_016860894.1:n.132+26C=
NM_014748.4:c.774+26C= MANE Select	NP_055563.1:n.774+26C=
NM_001267059.2:c.738+26C=	NP_001253988.1:n.738+26C=
NM_001267061.2:c.714+26C=	NP_001253990.1:n.714+26C=
NR_049782.2:n.1027+26C=
NR_049783.2:n.1000+26C=
NR_049784.2:n.976+26C=
NR_049785.2:n.909+26C=
NR_049786.2:n.858+26C=
NR_049787.2:n.709+26C=
NR_049788.2:n.639+26C=
NM_001267060.2:c.699+26C=	NP_001253989.1:n.699+26C=