Canonical Allele Identifier: CA1240248002

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375090C= , CM000664.2:g.27375090C=	GRCh38
NC_000002.11:g.27597957C= , CM000664.1:g.27597957C=	GRCh37
NC_000002.10:g.27451461C=	NCBI36
NG_009305.1:g.368G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.711C= MANE Select	ENSP00000233575.2:p.Ile237=
ENST00000233575.6:c.711C=	ENSP00000233575.2:p.Ile237=
ENST00000427123.5:c.*521C=	ENSP00000405399.1:n.*521C=
ENST00000440760.5:c.*556C=	ENSP00000399727.1:n.*556C=
ENST00000453453.1:c.*238C=	ENSP00000401922.1:n.*238C=
ENST00000493711.1:n.428C=
ENST00000494893.5:n.887C=
ENST00000537606.5:c.636C=	ENSP00000439208.1:p.Ile212=
NM_001267059.1:c.675C=	NP_001253988.1:p.Ile225=
NM_001267060.1:c.636C=	NP_001253989.1:p.Ile212=
NM_001267061.1:c.651C=	NP_001253990.1:p.Ile217=
NM_014748.3:c.711C=	NP_055563.1:p.Ile237=
NR_049782.1:n.1084C=
NR_049783.1:n.1057C=
NR_049784.1:n.1033C=
NR_049785.1:n.966C=
NR_049786.1:n.915C=
NR_049787.1:n.766C=
NR_049788.1:n.696C=
XM_011533203.1:c.69C=	XP_011531505.1:p.Ile23=
XM_011533203.2:c.69C=	XP_011531505.1:p.Ile23=
XM_017005405.2:c.69C=	XP_016860894.1:p.Ile23=
NM_014748.4:c.711C= MANE Select	NP_055563.1:p.Ile237=
NM_001267059.2:c.675C=	NP_001253988.1:p.Ile225=
NM_001267061.2:c.651C=	NP_001253990.1:p.Ile217=
NR_049782.2:n.964C=
NR_049783.2:n.937C=
NR_049784.2:n.913C=
NR_049785.2:n.846C=
NR_049786.2:n.795C=
NR_049787.2:n.646C=
NR_049788.2:n.576C=
NM_001267060.2:c.636C=	NP_001253989.1:p.Ile212=