Canonical Allele Identifier: CA12147766
Gene: TMEM232 HGNC NCBI

Linked Data

dbSNP Id: rs13360927

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.110700055A>G , CM000667.2:g.110700055A>G GRCh38
NC_000005.9:g.110035756A>G , CM000667.1:g.110035756A>G GRCh37
NC_000005.8:g.110063655A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000455884.7:c.-13+26572T>C MANE Select ENSP00000401477.2:n.-13+26572T>C
ENST00000455884.6:c.-13+26572T>C ENSP00000401477.2:n.-13+26572T>C
ENST00000502857.6:n.79+26572T>C
ENST00000503527.6:n.311-32691T>C
ENST00000511883.6:c.-48+26572T>C ENSP00000423904.2:n.-48+26572T>C
ENST00000512003.7:c.-13+26572T>C ENSP00000427785.2:n.-13+26572T>C
ENST00000512577.5:n.396+20471T>C
ENST00000512886.5:c.-12-32691T>C ENSP00000424807.1:n.-12-32691T>C
ENST00000515278.6:c.-13+26572T>C ENSP00000421614.2:n.-13+26572T>C
ENST00000515518.6:n.45+26572T>C
NM_001039763.3:c.-13+26572T>C NP_001034852.3:n.-13+26572T>C
XM_006714670.2:c.-13+26572T>C XP_006714733.1:n.-13+26572T>C
XM_011543552.1:c.-13+20471T>C XP_011541854.1:n.-13+20471T>C
XM_011543555.1:c.68+20471T>C XP_011541857.1:n.68+20471T>C
XM_011543556.1:c.68+20471T>C XP_011541858.1:n.68+20471T>C
XM_011543557.1:c.-13+20471T>C XP_011541859.1:n.-13+20471T>C
XM_011543558.1:c.-13+20471T>C XP_011541860.1:n.-13+20471T>C
XM_011543559.1:c.-13+20471T>C XP_011541861.1:n.-13+20471T>C
XM_011543561.1:c.-13+20471T>C XP_011541863.1:n.-13+20471T>C
XM_011543562.1:c.-13+20471T>C XP_011541864.1:n.-13+20471T>C
XM_011543563.1:c.-13+20471T>C XP_011541865.1:n.-13+20471T>C
XM_011543564.1:c.-13+20471T>C XP_011541866.1:n.-13+20471T>C
XM_011543565.1:c.-13+20471T>C XP_011541867.1:n.-13+20471T>C
XM_011543566.1:c.-216+26572T>C XP_011541868.1:n.-216+26572T>C
XM_011543567.1:c.-13+20471T>C XP_011541869.1:n.-13+20471T>C
XM_011543568.1:c.-230+26572T>C XP_011541870.1:n.-230+26572T>C
XR_948284.1:n.836+20471T>C
XR_948285.1:n.836+20471T>C
XR_948286.1:n.836+20471T>C
XR_948287.1:n.835+20471T>C
XM_006714670.3:c.-13+26572T>C XP_006714733.1:n.-13+26572T>C
XM_011543552.2:c.-13+20471T>C XP_011541854.1:n.-13+20471T>C
XM_011543555.2:c.68+20471T>C XP_011541857.1:n.68+20471T>C
XM_011543556.2:c.68+20471T>C XP_011541858.1:n.68+20471T>C
XM_011543557.2:c.-13+20471T>C XP_011541859.1:n.-13+20471T>C
XM_011543559.2:c.-13+20471T>C XP_011541861.1:n.-13+20471T>C
XM_011543561.2:c.-13+20471T>C XP_011541863.1:n.-13+20471T>C
XM_011543563.2:c.-13+20471T>C XP_011541865.1:n.-13+20471T>C
XM_011543564.3:c.-13+20471T>C XP_011541866.1:n.-13+20471T>C
XM_011543565.3:c.-13+20471T>C XP_011541867.1:n.-13+20471T>C
XM_011543566.2:c.-216+26572T>C XP_011541868.1:n.-216+26572T>C
XM_011543567.3:c.-13+20471T>C XP_011541869.1:n.-13+20471T>C
XM_017009705.2:c.-13+20471T>C XP_016865194.1:n.-13+20471T>C
XM_017009706.2:c.-13+20471T>C XP_016865195.1:n.-13+20471T>C
XM_017009707.1:c.-353+26572T>C XP_016865196.1:n.-353+26572T>C
XM_024446149.1:c.-13+26572T>C XP_024301917.1:n.-13+26572T>C
XR_001742181.1:n.850+20471T>C
XR_001742182.1:n.849+20471T>C
XR_948284.2:n.851+20471T>C
XR_948285.2:n.850+20471T>C
XR_948287.2:n.849+20471T>C
NM_001039763.4:c.-13+26572T>C MANE Select NP_001034852.3:n.-13+26572T>C