Canonical Allele Identifier: CA1240248721

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375527C= , CM000664.2:g.27375527C=	GRCh38
NC_000002.11:g.27598394C= , CM000664.1:g.27598394C=	GRCh37
NC_000002.10:g.27451898C=	NCBI36
NG_028219.1:g.10218G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.796C= MANE Select	ENSP00000233575.2:p.Leu266=
ENST00000233575.6:c.796C=	ENSP00000233575.2:p.Leu266=
ENST00000427123.5:c.*606C=	ENSP00000405399.1:n.*606C=
ENST00000440760.5:c.*641C=	ENSP00000399727.1:n.*641C=
ENST00000453453.1:c.*323C=	ENSP00000401922.1:n.*323C=
ENST00000493711.1:n.513C=
ENST00000537606.5:c.721C=	ENSP00000439208.1:p.Leu241=
NM_001267059.1:c.760C=	NP_001253988.1:p.Leu254=
NM_001267060.1:c.721C=	NP_001253989.1:p.Leu241=
NM_001267061.1:c.736C=	NP_001253990.1:p.Leu246=
NM_014748.3:c.796C=	NP_055563.1:p.Leu266=
NR_049782.1:n.1169C=
NR_049783.1:n.1142C=
NR_049784.1:n.1118C=
NR_049785.1:n.1051C=
NR_049786.1:n.1000C=
NR_049787.1:n.851C=
NR_049788.1:n.781C=
XM_011533203.1:c.154C=	XP_011531505.1:p.Leu52=
XM_011533203.2:c.154C=	XP_011531505.1:p.Leu52=
XM_017005405.2:c.154C=	XP_016860894.1:p.Leu52=
NM_014748.4:c.796C= MANE Select	NP_055563.1:p.Leu266=
NM_001267059.2:c.760C=	NP_001253988.1:p.Leu254=
NM_001267061.2:c.736C=	NP_001253990.1:p.Leu246=
NR_049782.2:n.1049C=
NR_049783.2:n.1022C=
NR_049784.2:n.998C=
NR_049785.2:n.931C=
NR_049786.2:n.880C=
NR_049787.2:n.731C=
NR_049788.2:n.661C=
NM_001267060.2:c.721C=	NP_001253989.1:p.Leu241=