Canonical Allele Identifier: CA425415784

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27597979C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375112C>A , CM000664.2:g.27375112C>A	GRCh38
NC_000002.11:g.27597979C>A , CM000664.1:g.27597979C>A	GRCh37
NC_000002.10:g.27451483C>A	NCBI36
NG_009305.1:g.346G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.733C>A MANE Select	ENSP00000233575.2:p.Arg245=
ENST00000233575.6:c.733C>A	ENSP00000233575.2:p.Arg245=
ENST00000427123.5:c.*543C>A	ENSP00000405399.1:n.*543C>A
ENST00000440760.5:c.*578C>A	ENSP00000399727.1:n.*578C>A
ENST00000453453.1:c.*260C>A	ENSP00000401922.1:n.*260C>A
ENST00000493711.1:n.450C>A
ENST00000494893.5:n.909C>A
ENST00000537606.5:c.658C>A	ENSP00000439208.1:p.Arg220=
NM_001267059.1:c.697C>A	NP_001253988.1:p.Arg233=
NM_001267060.1:c.658C>A	NP_001253989.1:p.Arg220=
NM_001267061.1:c.673C>A	NP_001253990.1:p.Arg225=
NM_014748.3:c.733C>A	NP_055563.1:p.Arg245=
NR_049782.1:n.1106C>A
NR_049783.1:n.1079C>A
NR_049784.1:n.1055C>A
NR_049785.1:n.988C>A
NR_049786.1:n.937C>A
NR_049787.1:n.788C>A
NR_049788.1:n.718C>A
XM_011533203.1:c.91C>A	XP_011531505.1:p.Arg31=
XM_011533203.2:c.91C>A	XP_011531505.1:p.Arg31=
XM_017005405.2:c.91C>A	XP_016860894.1:p.Arg31=
NM_014748.4:c.733C>A MANE Select	NP_055563.1:p.Arg245=
NM_001267059.2:c.697C>A	NP_001253988.1:p.Arg233=
NM_001267061.2:c.673C>A	NP_001253990.1:p.Arg225=
NR_049782.2:n.986C>A
NR_049783.2:n.959C>A
NR_049784.2:n.935C>A
NR_049785.2:n.868C>A
NR_049786.2:n.817C>A
NR_049787.2:n.668C>A
NR_049788.2:n.598C>A
NM_001267060.2:c.658C>A	NP_001253989.1:p.Arg220=