Canonical Allele Identifier: CA1240248122

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375202G= , CM000664.2:g.27375202G=	GRCh38
NC_000002.11:g.27598069G= , CM000664.1:g.27598069G=	GRCh37
NC_000002.10:g.27451573G=	NCBI36
NG_009305.1:g.256C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.774+49G= MANE Select	ENSP00000233575.2:n.774+49G=
ENST00000233575.6:c.774+49G=	ENSP00000233575.2:n.774+49G=
ENST00000427123.5:c.*584+49G=	ENSP00000405399.1:n.*584+49G=
ENST00000440760.5:c.*619+49G=	ENSP00000399727.1:n.*619+49G=
ENST00000453453.1:c.*301+49G=	ENSP00000401922.1:n.*301+49G=
ENST00000493711.1:n.491+49G=
ENST00000494893.5:n.950+49G=
ENST00000537606.5:c.699+49G=	ENSP00000439208.1:n.699+49G=
NM_001267059.1:c.738+49G=	NP_001253988.1:n.738+49G=
NM_001267060.1:c.699+49G=	NP_001253989.1:n.699+49G=
NM_001267061.1:c.714+49G=	NP_001253990.1:n.714+49G=
NM_014748.3:c.774+49G=	NP_055563.1:n.774+49G=
NR_049782.1:n.1147+49G=
NR_049783.1:n.1120+49G=
NR_049784.1:n.1096+49G=
NR_049785.1:n.1029+49G=
NR_049786.1:n.978+49G=
NR_049787.1:n.829+49G=
NR_049788.1:n.759+49G=
XM_011533203.1:c.132+49G=	XP_011531505.1:n.132+49G=
XM_011533203.2:c.132+49G=	XP_011531505.1:n.132+49G=
XM_017005405.2:c.132+49G=	XP_016860894.1:n.132+49G=
NM_014748.4:c.774+49G= MANE Select	NP_055563.1:n.774+49G=
NM_001267059.2:c.738+49G=	NP_001253988.1:n.738+49G=
NM_001267061.2:c.714+49G=	NP_001253990.1:n.714+49G=
NR_049782.2:n.1027+49G=
NR_049783.2:n.1000+49G=
NR_049784.2:n.976+49G=
NR_049785.2:n.909+49G=
NR_049786.2:n.858+49G=
NR_049787.2:n.709+49G=
NR_049788.2:n.639+49G=
NM_001267060.2:c.699+49G=	NP_001253989.1:n.699+49G=