Canonical Allele Identifier: CA454347479

Gene: SNX10

Linked Data

• gnomAD v4: 7-26364564-A-T
• MyVariant Identifiers: chr7:g.26404184A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.26364564A>T , CM000669.2:g.26364564A>T	GRCh38
NC_000007.13:g.26404184A>T , CM000669.1:g.26404184A>T	GRCh37
NC_000007.12:g.26370709A>T	NCBI36
NG_033902.1:g.77670A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409367.6:c.21A>T	ENSP00000387274.1:p.Thr7=
ENST00000416246.6:c.21A>T	ENSP00000408164.2:p.Thr7=
ENST00000698074.1:c.21A>T	ENSP00000513546.1:p.Thr7=
ENST00000698075.1:c.21A>T	ENSP00000513547.1:p.Thr7=
ENST00000698076.1:c.21A>T	ENSP00000513548.1:p.Thr7=
ENST00000698077.1:c.141A>T	ENSP00000513549.1:p.Thr47=
ENST00000698078.1:c.141A>T	ENSP00000513550.1:p.Thr47=
ENST00000698079.1:c.141A>T	ENSP00000513551.1:p.Thr47=
ENST00000698080.1:c.141A>T	ENSP00000513552.1:p.Thr47=
ENST00000698081.1:c.141A>T	ENSP00000513553.1:p.Thr47=
ENST00000698082.1:n.250A>T
ENST00000698083.1:c.141A>T	ENSP00000513554.1:p.Thr47=
ENST00000698084.1:c.21A>T	ENSP00000513555.1:p.Thr7=
ENST00000698085.1:n.237A>T
ENST00000698086.1:c.141A>T	ENSP00000513556.1:p.Thr47=
ENST00000698087.1:c.141A>T	ENSP00000513557.1:p.Thr47=
ENST00000698088.1:c.141A>T	ENSP00000513558.1:p.Thr47=
ENST00000698089.1:c.21A>T	ENSP00000513559.1:p.Thr7=
ENST00000698090.1:c.141A>T	ENSP00000513560.1:p.Thr47=
ENST00000698091.1:n.2001A>T
ENST00000338523.9:c.141A>T MANE Select	ENSP00000343709.5:p.Thr47=
ENST00000338523.8:c.141A>T	ENSP00000343709.4:p.Thr47=
ENST00000396376.5:c.141A>T	ENSP00000379661.1:p.Thr47=
ENST00000409367.5:c.21A>T	ENSP00000387274.1:p.Thr7=
ENST00000409838.1:c.-41+62A>T	ENSP00000386540.1:n.-41+62A>T
ENST00000416246.5:c.219A>T	ENSP00000408164.1:p.Thr73=
ENST00000446848.6:c.141A>T	ENSP00000395474.3:p.Thr47=
ENST00000619420.4:c.141A>T	ENSP00000478710.1:p.Thr47=
NM_001199835.1:c.141A>T	NP_001186764.1:p.Thr47=
NM_001199837.1:c.132A>T	NP_001186766.1:p.Thr44=
NM_001199838.1:c.-41+62A>T	NP_001186767.1:n.-41+62A>T
NM_013322.2:c.141A>T	NP_037454.2:p.Thr47=
NR_037670.1:n.477A>T
XM_006715710.1:c.141A>T	XP_006715773.1:p.Thr47=
XM_006715711.1:c.141A>T	XP_006715774.1:p.Thr47=
XM_006715712.1:c.141A>T	XP_006715775.1:p.Thr47=
NM_001318198.1:c.219A>T	NP_001305127.1:p.Thr73=
NM_001318199.1:c.141A>T	NP_001305128.1:p.Thr47=
NM_001362753.1:c.219A>T	NP_001349682.1:p.Thr73=
NM_001362754.1:c.219A>T	NP_001349683.1:p.Thr73=
XM_006715712.2:c.141A>T	XP_006715775.1:p.Thr47=
XM_017012086.1:c.219A>T	XP_016867575.1:p.Thr73=
NM_001199837.2:c.132A>T	NP_001186766.1:p.Thr44=
NM_001318199.2:c.141A>T	NP_001305128.1:p.Thr47=
NM_013322.3:c.141A>T MANE Select	NP_037454.2:p.Thr47=
NM_001199837.3:c.132A>T	NP_001186766.1:p.Thr44=
NM_001199838.2:c.-41+62A>T	NP_001186767.1:n.-41+62A>T
NM_001318199.3:c.141A>T	NP_001305128.1:p.Thr47=