Canonical Allele Identifier: CA4195197

Gene: SNX10

Linked Data

• dbSNP Id: rs772724819
• ExAC: 7:26404256 G / T
• gnomAD v2: 7-26404256-G-T
• gnomAD v4: 7-26364636-G-T
• MyVariant Identifiers: chr7:g.26404256G>T (hg19) ; chr7:g.26364636G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.26364636G>T , CM000669.2:g.26364636G>T	GRCh38
NC_000007.13:g.26404256G>T , CM000669.1:g.26404256G>T	GRCh37
NC_000007.12:g.26370781G>T	NCBI36
NG_033902.1:g.77742G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000409367.6:c.92+1G>T	ENSP00000387274.1:n.92+1G>T
ENST00000416246.6:c.92+1G>T	ENSP00000408164.2:n.92+1G>T
ENST00000698074.1:c.92+1G>T	ENSP00000513546.1:n.92+1G>T
ENST00000698075.1:c.92+1G>T	ENSP00000513547.1:n.92+1G>T
ENST00000698076.1:c.92+1G>T	ENSP00000513548.1:n.92+1G>T
ENST00000698077.1:c.212+1G>T	ENSP00000513549.1:n.212+1G>T
ENST00000698078.1:c.212+1G>T	ENSP00000513550.1:n.212+1G>T
ENST00000698079.1:c.212+1G>T	ENSP00000513551.1:n.212+1G>T
ENST00000698080.1:c.212+1G>T	ENSP00000513552.1:n.212+1G>T
ENST00000698081.1:c.212+1G>T	ENSP00000513553.1:n.212+1G>T
ENST00000698082.1:n.321+1G>T
ENST00000698083.1:c.196+17G>T	ENSP00000513554.1:n.196+17G>T
ENST00000698084.1:c.92+1G>T	ENSP00000513555.1:n.92+1G>T
ENST00000698085.1:n.309G>T
ENST00000698086.1:c.212+1G>T	ENSP00000513556.1:n.212+1G>T
ENST00000698087.1:c.212+1G>T	ENSP00000513557.1:n.212+1G>T
ENST00000698088.1:c.212+1G>T	ENSP00000513558.1:n.212+1G>T
ENST00000698089.1:c.92+1G>T	ENSP00000513559.1:n.92+1G>T
ENST00000698090.1:c.212+1G>T	ENSP00000513560.1:n.212+1G>T
ENST00000698091.1:n.2072+1G>T
ENST00000698092.1:n.68+1G>T
ENST00000338523.9:c.212+1G>T MANE Select	ENSP00000343709.5:n.212+1G>T
ENST00000338523.8:c.212+1G>T	ENSP00000343709.4:n.212+1G>T
ENST00000396376.5:c.212+1G>T	ENSP00000379661.1:n.212+1G>T
ENST00000409367.5:c.92+1G>T	ENSP00000387274.1:n.92+1G>T
ENST00000409838.1:c.-41+134G>T	ENSP00000386540.1:n.-41+134G>T
ENST00000416246.5:c.290+1G>T	ENSP00000408164.1:n.290+1G>T
ENST00000446848.6:c.212+1G>T	ENSP00000395474.3:n.212+1G>T
ENST00000619420.4:c.212+1G>T	ENSP00000478710.1:n.212+1G>T
NM_001199835.1:c.212+1G>T	NP_001186764.1:n.212+1G>T
NM_001199837.1:c.203+1G>T	NP_001186766.1:n.203+1G>T
NM_001199838.1:c.-41+134G>T	NP_001186767.1:n.-41+134G>T
NM_013322.2:c.212+1G>T	NP_037454.2:n.212+1G>T
NR_037670.1:n.548+1G>T
XM_006715710.1:c.212+1G>T	XP_006715773.1:n.212+1G>T
XM_006715711.1:c.212+1G>T	XP_006715774.1:n.212+1G>T
XM_006715712.1:c.212+1G>T	XP_006715775.1:n.212+1G>T
NM_001318198.1:c.290+1G>T	NP_001305127.1:n.290+1G>T
NM_001318199.1:c.212+1G>T	NP_001305128.1:n.212+1G>T
NM_001362753.1:c.290+1G>T	NP_001349682.1:n.290+1G>T
NM_001362754.1:c.290+1G>T	NP_001349683.1:n.290+1G>T
XM_006715712.2:c.212+1G>T	XP_006715775.1:n.212+1G>T
XM_017012086.1:c.290+1G>T	XP_016867575.1:n.290+1G>T
NM_001199837.2:c.203+1G>T	NP_001186766.1:n.203+1G>T
NM_001318199.2:c.212+1G>T	NP_001305128.1:n.212+1G>T
NM_013322.3:c.212+1G>T MANE Select	NP_037454.2:n.212+1G>T
NM_001199837.3:c.203+1G>T	NP_001186766.1:n.203+1G>T
NM_001199838.2:c.-41+134G>T	NP_001186767.1:n.-41+134G>T
NM_001318199.3:c.212+1G>T	NP_001305128.1:n.212+1G>T