Canonical Allele Identifier: CA367228157

Gene: SNX10

Linked Data

• MyVariant Identifiers: chr7:g.26404219G>C (hg19) ; chr7:g.26364599G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.26364599G>C , CM000669.2:g.26364599G>C	GRCh38
NC_000007.13:g.26404219G>C , CM000669.1:g.26404219G>C	GRCh37
NC_000007.12:g.26370744G>C	NCBI36
NG_033902.1:g.77705G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409367.6:c.56G>C	ENSP00000387274.1:p.Trp19Ser
ENST00000416246.6:c.56G>C	ENSP00000408164.2:p.Trp19Ser
ENST00000698074.1:c.56G>C	ENSP00000513546.1:p.Trp19Ser
ENST00000698075.1:c.56G>C	ENSP00000513547.1:p.Trp19Ser
ENST00000698076.1:c.56G>C	ENSP00000513548.1:p.Trp19Ser
ENST00000698077.1:c.176G>C	ENSP00000513549.1:p.Trp59Ser
ENST00000698078.1:c.176G>C	ENSP00000513550.1:p.Trp59Ser
ENST00000698079.1:c.176G>C	ENSP00000513551.1:p.Trp59Ser
ENST00000698080.1:c.176G>C	ENSP00000513552.1:p.Trp59Ser
ENST00000698081.1:c.176G>C	ENSP00000513553.1:p.Trp59Ser
ENST00000698082.1:n.285G>C
ENST00000698083.1:c.176G>C	ENSP00000513554.1:p.Trp59Ser
ENST00000698084.1:c.56G>C	ENSP00000513555.1:p.Trp19Ser
ENST00000698085.1:n.272G>C
ENST00000698086.1:c.176G>C	ENSP00000513556.1:p.Trp59Ser
ENST00000698087.1:c.176G>C	ENSP00000513557.1:p.Trp59Ser
ENST00000698088.1:c.176G>C	ENSP00000513558.1:p.Trp59Ser
ENST00000698089.1:c.56G>C	ENSP00000513559.1:p.Trp19Ser
ENST00000698090.1:c.176G>C	ENSP00000513560.1:p.Trp59Ser
ENST00000698091.1:n.2036G>C
ENST00000698092.1:n.32G>C
ENST00000338523.9:c.176G>C MANE Select	ENSP00000343709.5:p.Trp59Ser
ENST00000338523.8:c.176G>C	ENSP00000343709.4:p.Trp59Ser
ENST00000396376.5:c.176G>C	ENSP00000379661.1:p.Trp59Ser
ENST00000409367.5:c.56G>C	ENSP00000387274.1:p.Trp19Ser
ENST00000409838.1:c.-41+97G>C	ENSP00000386540.1:n.-41+97G>C
ENST00000416246.5:c.254G>C	ENSP00000408164.1:p.Trp85Ser
ENST00000446848.6:c.176G>C	ENSP00000395474.3:p.Trp59Ser
ENST00000619420.4:c.176G>C	ENSP00000478710.1:p.Trp59Ser
NM_001199835.1:c.176G>C	NP_001186764.1:p.Trp59Ser
NM_001199837.1:c.167G>C	NP_001186766.1:p.Trp56Ser
NM_001199838.1:c.-41+97G>C	NP_001186767.1:n.-41+97G>C
NM_013322.2:c.176G>C	NP_037454.2:p.Trp59Ser
NR_037670.1:n.512G>C
XM_006715710.1:c.176G>C	XP_006715773.1:p.Trp59Ser
XM_006715711.1:c.176G>C	XP_006715774.1:p.Trp59Ser
XM_006715712.1:c.176G>C	XP_006715775.1:p.Trp59Ser
NM_001318198.1:c.254G>C	NP_001305127.1:p.Trp85Ser
NM_001318199.1:c.176G>C	NP_001305128.1:p.Trp59Ser
NM_001362753.1:c.254G>C	NP_001349682.1:p.Trp85Ser
NM_001362754.1:c.254G>C	NP_001349683.1:p.Trp85Ser
XM_006715712.2:c.176G>C	XP_006715775.1:p.Trp59Ser
XM_017012086.1:c.254G>C	XP_016867575.1:p.Trp85Ser
NM_001199837.2:c.167G>C	NP_001186766.1:p.Trp56Ser
NM_001318199.2:c.176G>C	NP_001305128.1:p.Trp59Ser
NM_013322.3:c.176G>C MANE Select	NP_037454.2:p.Trp59Ser
NM_001199837.3:c.167G>C	NP_001186766.1:p.Trp56Ser
NM_001199838.2:c.-41+97G>C	NP_001186767.1:n.-41+97G>C
NM_001318199.3:c.176G>C	NP_001305128.1:p.Trp59Ser