Canonical Allele Identifier: CA454347656

Gene: SNX10

Linked Data

• MyVariant Identifiers: chr7:g.26404235C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.26364615C>T , CM000669.2:g.26364615C>T	GRCh38
NC_000007.13:g.26404235C>T , CM000669.1:g.26404235C>T	GRCh37
NC_000007.12:g.26370760C>T	NCBI36
NG_033902.1:g.77721C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409367.6:c.72C>T	ENSP00000387274.1:p.Leu24=
ENST00000416246.6:c.72C>T	ENSP00000408164.2:p.Leu24=
ENST00000698074.1:c.72C>T	ENSP00000513546.1:p.Leu24=
ENST00000698075.1:c.72C>T	ENSP00000513547.1:p.Leu24=
ENST00000698076.1:c.72C>T	ENSP00000513548.1:p.Leu24=
ENST00000698077.1:c.192C>T	ENSP00000513549.1:p.Leu64=
ENST00000698078.1:c.192C>T	ENSP00000513550.1:p.Leu64=
ENST00000698079.1:c.192C>T	ENSP00000513551.1:p.Leu64=
ENST00000698080.1:c.192C>T	ENSP00000513552.1:p.Leu64=
ENST00000698081.1:c.192C>T	ENSP00000513553.1:p.Leu64=
ENST00000698082.1:n.301C>T
ENST00000698083.1:c.192C>T	ENSP00000513554.1:p.Leu64=
ENST00000698084.1:c.72C>T	ENSP00000513555.1:p.Leu24=
ENST00000698085.1:n.288C>T
ENST00000698086.1:c.192C>T	ENSP00000513556.1:p.Leu64=
ENST00000698087.1:c.192C>T	ENSP00000513557.1:p.Leu64=
ENST00000698088.1:c.192C>T	ENSP00000513558.1:p.Leu64=
ENST00000698089.1:c.72C>T	ENSP00000513559.1:p.Leu24=
ENST00000698090.1:c.192C>T	ENSP00000513560.1:p.Leu64=
ENST00000698091.1:n.2052C>T
ENST00000698092.1:n.48C>T
ENST00000338523.9:c.192C>T MANE Select	ENSP00000343709.5:p.Leu64=
ENST00000338523.8:c.192C>T	ENSP00000343709.4:p.Leu64=
ENST00000396376.5:c.192C>T	ENSP00000379661.1:p.Leu64=
ENST00000409367.5:c.72C>T	ENSP00000387274.1:p.Leu24=
ENST00000409838.1:c.-41+113C>T	ENSP00000386540.1:n.-41+113C>T
ENST00000416246.5:c.270C>T	ENSP00000408164.1:p.Leu90=
ENST00000446848.6:c.192C>T	ENSP00000395474.3:p.Leu64=
ENST00000619420.4:c.192C>T	ENSP00000478710.1:p.Leu64=
NM_001199835.1:c.192C>T	NP_001186764.1:p.Leu64=
NM_001199837.1:c.183C>T	NP_001186766.1:p.Leu61=
NM_001199838.1:c.-41+113C>T	NP_001186767.1:n.-41+113C>T
NM_013322.2:c.192C>T	NP_037454.2:p.Leu64=
NR_037670.1:n.528C>T
XM_006715710.1:c.192C>T	XP_006715773.1:p.Leu64=
XM_006715711.1:c.192C>T	XP_006715774.1:p.Leu64=
XM_006715712.1:c.192C>T	XP_006715775.1:p.Leu64=
NM_001318198.1:c.270C>T	NP_001305127.1:p.Leu90=
NM_001318199.1:c.192C>T	NP_001305128.1:p.Leu64=
NM_001362753.1:c.270C>T	NP_001349682.1:p.Leu90=
NM_001362754.1:c.270C>T	NP_001349683.1:p.Leu90=
XM_006715712.2:c.192C>T	XP_006715775.1:p.Leu64=
XM_017012086.1:c.270C>T	XP_016867575.1:p.Leu90=
NM_001199837.2:c.183C>T	NP_001186766.1:p.Leu61=
NM_001318199.2:c.192C>T	NP_001305128.1:p.Leu64=
NM_013322.3:c.192C>T MANE Select	NP_037454.2:p.Leu64=
NM_001199837.3:c.183C>T	NP_001186766.1:p.Leu61=
NM_001199838.2:c.-41+113C>T	NP_001186767.1:n.-41+113C>T
NM_001318199.3:c.192C>T	NP_001305128.1:p.Leu64=