Canonical Allele Identifier: CA2515886860

Gene: TMEM232

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110713297_110713298insCCTGTG , CM000667.2:g.110713297_110713298insCCTGTG	GRCh38
NC_000005.9:g.110048998_110048999insCCTGTG , CM000667.1:g.110048998_110048999insCCTGTG	GRCh37
NC_000005.8:g.110076897_110076898insCCTGTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455884.7:c.-13+13329_-13+13330insCACAGG MANE Select	ENSP00000401477.2:n.-13+13329_-13+13330insCACAGG
ENST00000455884.6:c.-13+13329_-13+13330insCACAGG	ENSP00000401477.2:n.-13+13329_-13+13330insCACAGG
ENST00000502857.6:n.79+13329_79+13330insCACAGG
ENST00000503527.6:n.310+21605_310+21606insCACAGG
ENST00000511883.6:c.-48+13329_-48+13330insCACAGG	ENSP00000423904.2:n.-48+13329_-48+13330insCACAGG
ENST00000512003.7:c.-13+13329_-13+13330insCACAGG	ENSP00000427785.2:n.-13+13329_-13+13330insCACAGG
ENST00000512577.5:n.396+7228_396+7229insCACAGG
ENST00000512886.5:c.-13+21605_-13+21606insCACAGG	ENSP00000424807.1:n.-13+21605_-13+21606insCACAGG
ENST00000515278.6:c.-13+13329_-13+13330insCACAGG	ENSP00000421614.2:n.-13+13329_-13+13330insCACAGG
ENST00000515518.6:n.45+13329_45+13330insCACAGG
NM_001039763.3:c.-13+13329_-13+13330insCACAGG	NP_001034852.3:n.-13+13329_-13+13330insCACAGG
XM_006714670.2:c.-13+13329_-13+13330insCACAGG	XP_006714733.1:n.-13+13329_-13+13330insCACAGG
XM_011543552.1:c.-13+7228_-13+7229insCACAGG	XP_011541854.1:n.-13+7228_-13+7229insCACAGG
XM_011543555.1:c.68+7228_68+7229insCACAGG	XP_011541857.1:n.68+7228_68+7229insCACAGG
XM_011543556.1:c.68+7228_68+7229insCACAGG	XP_011541858.1:n.68+7228_68+7229insCACAGG
XM_011543557.1:c.-13+7228_-13+7229insCACAGG	XP_011541859.1:n.-13+7228_-13+7229insCACAGG
XM_011543558.1:c.-13+7228_-13+7229insCACAGG	XP_011541860.1:n.-13+7228_-13+7229insCACAGG
XM_011543559.1:c.-13+7228_-13+7229insCACAGG	XP_011541861.1:n.-13+7228_-13+7229insCACAGG
XM_011543561.1:c.-13+7228_-13+7229insCACAGG	XP_011541863.1:n.-13+7228_-13+7229insCACAGG
XM_011543562.1:c.-13+7228_-13+7229insCACAGG	XP_011541864.1:n.-13+7228_-13+7229insCACAGG
XM_011543563.1:c.-13+7228_-13+7229insCACAGG	XP_011541865.1:n.-13+7228_-13+7229insCACAGG
XM_011543564.1:c.-13+7228_-13+7229insCACAGG	XP_011541866.1:n.-13+7228_-13+7229insCACAGG
XM_011543565.1:c.-13+7228_-13+7229insCACAGG	XP_011541867.1:n.-13+7228_-13+7229insCACAGG
XM_011543566.1:c.-216+13329_-216+13330insCACAGG	XP_011541868.1:n.-216+13329_-216+13330insCACAGG
XM_011543567.1:c.-13+7228_-13+7229insCACAGG	XP_011541869.1:n.-13+7228_-13+7229insCACAGG
XM_011543568.1:c.-230+13329_-230+13330insCACAGG	XP_011541870.1:n.-230+13329_-230+13330insCACAGG
XR_948284.1:n.836+7228_836+7229insCACAGG
XR_948285.1:n.836+7228_836+7229insCACAGG
XR_948286.1:n.836+7228_836+7229insCACAGG
XR_948287.1:n.835+7228_835+7229insCACAGG
XM_006714670.3:c.-13+13329_-13+13330insCACAGG	XP_006714733.1:n.-13+13329_-13+13330insCACAGG
XM_011543552.2:c.-13+7228_-13+7229insCACAGG	XP_011541854.1:n.-13+7228_-13+7229insCACAGG
XM_011543555.2:c.68+7228_68+7229insCACAGG	XP_011541857.1:n.68+7228_68+7229insCACAGG
XM_011543556.2:c.68+7228_68+7229insCACAGG	XP_011541858.1:n.68+7228_68+7229insCACAGG
XM_011543557.2:c.-13+7228_-13+7229insCACAGG	XP_011541859.1:n.-13+7228_-13+7229insCACAGG
XM_011543559.2:c.-13+7228_-13+7229insCACAGG	XP_011541861.1:n.-13+7228_-13+7229insCACAGG
XM_011543561.2:c.-13+7228_-13+7229insCACAGG	XP_011541863.1:n.-13+7228_-13+7229insCACAGG
XM_011543563.2:c.-13+7228_-13+7229insCACAGG	XP_011541865.1:n.-13+7228_-13+7229insCACAGG
XM_011543564.3:c.-13+7228_-13+7229insCACAGG	XP_011541866.1:n.-13+7228_-13+7229insCACAGG
XM_011543565.3:c.-13+7228_-13+7229insCACAGG	XP_011541867.1:n.-13+7228_-13+7229insCACAGG
XM_011543566.2:c.-216+13329_-216+13330insCACAGG	XP_011541868.1:n.-216+13329_-216+13330insCACAGG
XM_011543567.3:c.-13+7228_-13+7229insCACAGG	XP_011541869.1:n.-13+7228_-13+7229insCACAGG
XM_017009705.2:c.-13+7228_-13+7229insCACAGG	XP_016865194.1:n.-13+7228_-13+7229insCACAGG
XM_017009706.2:c.-13+7228_-13+7229insCACAGG	XP_016865195.1:n.-13+7228_-13+7229insCACAGG
XM_017009707.1:c.-353+13329_-353+13330insCACAGG	XP_016865196.1:n.-353+13329_-353+13330insCACAGG
XM_024446149.1:c.-13+13329_-13+13330insCACAGG	XP_024301917.1:n.-13+13329_-13+13330insCACAGG
XR_001742181.1:n.850+7228_850+7229insCACAGG
XR_001742182.1:n.849+7228_849+7229insCACAGG
XR_948284.2:n.851+7228_851+7229insCACAGG
XR_948285.2:n.850+7228_850+7229insCACAGG
XR_948287.2:n.849+7228_849+7229insCACAGG
NM_001039763.4:c.-13+13329_-13+13330insCACAGG MANE Select	NP_001034852.3:n.-13+13329_-13+13330insCACAGG