Canonical Allele Identifier: CA1240248050

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375139G= , CM000664.2:g.27375139G=	GRCh38
NC_000002.11:g.27598006G= , CM000664.1:g.27598006G=	GRCh37
NC_000002.10:g.27451510G=	NCBI36
NG_009305.1:g.319C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.760G= MANE Select	ENSP00000233575.2:p.Val254=
ENST00000233575.6:c.760G=	ENSP00000233575.2:p.Val254=
ENST00000427123.5:c.*570G=	ENSP00000405399.1:n.*570G=
ENST00000440760.5:c.*605G=	ENSP00000399727.1:n.*605G=
ENST00000453453.1:c.*287G=	ENSP00000401922.1:n.*287G=
ENST00000493711.1:n.477G=
ENST00000494893.5:n.936G=
ENST00000537606.5:c.685G=	ENSP00000439208.1:p.Val229=
NM_001267059.1:c.724G=	NP_001253988.1:p.Val242=
NM_001267060.1:c.685G=	NP_001253989.1:p.Val229=
NM_001267061.1:c.700G=	NP_001253990.1:p.Val234=
NM_014748.3:c.760G=	NP_055563.1:p.Val254=
NR_049782.1:n.1133G=
NR_049783.1:n.1106G=
NR_049784.1:n.1082G=
NR_049785.1:n.1015G=
NR_049786.1:n.964G=
NR_049787.1:n.815G=
NR_049788.1:n.745G=
XM_011533203.1:c.118G=	XP_011531505.1:p.Val40=
XM_011533203.2:c.118G=	XP_011531505.1:p.Val40=
XM_017005405.2:c.118G=	XP_016860894.1:p.Val40=
NM_014748.4:c.760G= MANE Select	NP_055563.1:p.Val254=
NM_001267059.2:c.724G=	NP_001253988.1:p.Val242=
NM_001267061.2:c.700G=	NP_001253990.1:p.Val234=
NR_049782.2:n.1013G=
NR_049783.2:n.986G=
NR_049784.2:n.962G=
NR_049785.2:n.895G=
NR_049786.2:n.844G=
NR_049787.2:n.695G=
NR_049788.2:n.625G=
NM_001267060.2:c.685G=	NP_001253989.1:p.Val229=