Canonical Allele Identifier: CA1240249383

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375033T= , CM000664.2:g.27375033T=	GRCh38
NC_000002.11:g.27597900T= , CM000664.1:g.27597900T=	GRCh37
NC_000002.10:g.27451404T=	NCBI36
NG_009305.1:g.425A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.682-28T= MANE Select	ENSP00000233575.2:n.682-28T=
ENST00000233575.6:c.682-28T=	ENSP00000233575.2:n.682-28T=
ENST00000427123.5:c.*492-28T=	ENSP00000405399.1:n.*492-28T=
ENST00000440760.5:c.*527-28T=	ENSP00000399727.1:n.*527-28T=
ENST00000453453.1:c.*209-28T=	ENSP00000401922.1:n.*209-28T=
ENST00000493711.1:n.371T=
ENST00000494893.5:n.858-28T=
ENST00000537606.5:c.607-28T=	ENSP00000439208.1:n.607-28T=
NM_001267059.1:c.646-28T=	NP_001253988.1:n.646-28T=
NM_001267060.1:c.607-28T=	NP_001253989.1:n.607-28T=
NM_001267061.1:c.622-28T=	NP_001253990.1:n.622-28T=
NM_014748.3:c.682-28T=	NP_055563.1:n.682-28T=
NR_049782.1:n.1055-28T=
NR_049783.1:n.1028-28T=
NR_049784.1:n.1004-28T=
NR_049785.1:n.937-28T=
NR_049786.1:n.886-28T=
NR_049787.1:n.737-28T=
NR_049788.1:n.667-28T=
XM_011533203.1:c.40-28T=	XP_011531505.1:n.40-28T=
XM_011533203.2:c.40-28T=	XP_011531505.1:n.40-28T=
XM_017005405.2:c.40-28T=	XP_016860894.1:n.40-28T=
NM_014748.4:c.682-28T= MANE Select	NP_055563.1:n.682-28T=
NM_001267059.2:c.646-28T=	NP_001253988.1:n.646-28T=
NM_001267061.2:c.622-28T=	NP_001253990.1:n.622-28T=
NR_049782.2:n.935-28T=
NR_049783.2:n.908-28T=
NR_049784.2:n.884-28T=
NR_049785.2:n.817-28T=
NR_049786.2:n.766-28T=
NR_049787.2:n.617-28T=
NR_049788.2:n.547-28T=
NM_001267060.2:c.607-28T=	NP_001253989.1:n.607-28T=