Canonical Allele Identifier: CA425415788

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27597981G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375114G>C , CM000664.2:g.27375114G>C	GRCh38
NC_000002.11:g.27597981G>C , CM000664.1:g.27597981G>C	GRCh37
NC_000002.10:g.27451485G>C	NCBI36
NG_009305.1:g.344C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.735G>C MANE Select	ENSP00000233575.2:p.Arg245=
ENST00000233575.6:c.735G>C	ENSP00000233575.2:p.Arg245=
ENST00000427123.5:c.*545G>C	ENSP00000405399.1:n.*545G>C
ENST00000440760.5:c.*580G>C	ENSP00000399727.1:n.*580G>C
ENST00000453453.1:c.*262G>C	ENSP00000401922.1:n.*262G>C
ENST00000493711.1:n.452G>C
ENST00000494893.5:n.911G>C
ENST00000537606.5:c.660G>C	ENSP00000439208.1:p.Arg220=
NM_001267059.1:c.699G>C	NP_001253988.1:p.Arg233=
NM_001267060.1:c.660G>C	NP_001253989.1:p.Arg220=
NM_001267061.1:c.675G>C	NP_001253990.1:p.Arg225=
NM_014748.3:c.735G>C	NP_055563.1:p.Arg245=
NR_049782.1:n.1108G>C
NR_049783.1:n.1081G>C
NR_049784.1:n.1057G>C
NR_049785.1:n.990G>C
NR_049786.1:n.939G>C
NR_049787.1:n.790G>C
NR_049788.1:n.720G>C
XM_011533203.1:c.93G>C	XP_011531505.1:p.Arg31=
XM_011533203.2:c.93G>C	XP_011531505.1:p.Arg31=
XM_017005405.2:c.93G>C	XP_016860894.1:p.Arg31=
NM_014748.4:c.735G>C MANE Select	NP_055563.1:p.Arg245=
NM_001267059.2:c.699G>C	NP_001253988.1:p.Arg233=
NM_001267061.2:c.675G>C	NP_001253990.1:p.Arg225=
NR_049782.2:n.988G>C
NR_049783.2:n.961G>C
NR_049784.2:n.937G>C
NR_049785.2:n.870G>C
NR_049786.2:n.819G>C
NR_049787.2:n.670G>C
NR_049788.2:n.600G>C
NM_001267060.2:c.660G>C	NP_001253989.1:p.Arg220=