Canonical Allele Identifier: CA2709723356

Gene: TMEM232

Linked Data

• dbSNP Id: rs202026258

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110490731_110490735dup , CM000667.2:g.110490731_110490735dup	GRCh38
NC_000005.9:g.109826432_109826436dup , CM000667.1:g.109826432_109826436dup	GRCh37
NC_000005.8:g.109854331_109854335dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455884.7:c.1703+37855_1703+37859dup MANE Select	ENSP00000401477.2:n.1703+37855_1703+37859dup
ENST00000455884.6:c.1703+37855_1703+37859dup	ENSP00000401477.2:n.1703+37855_1703+37859dup
ENST00000508571.6:n.1018+77714_1018+77718dup
ENST00000512003.7:c.*998-65817_*998-65813dup	ENSP00000427785.2:n.*998-65817_*998-65813dup
ENST00000515518.6:n.1376-65817_1376-65813dup
NM_001039763.3:c.1703+37855_1703+37859dup	NP_001034852.3:n.1703+37855_1703+37859dup
XM_006714670.2:c.1703+37855_1703+37859dup	XP_006714733.1:n.1703+37855_1703+37859dup
XM_011543552.1:c.1703+37855_1703+37859dup	XP_011541854.1:n.1703+37855_1703+37859dup
XM_011543553.1:c.1703+37855_1703+37859dup	XP_011541855.1:n.1703+37855_1703+37859dup
XM_011543554.1:c.1703+37855_1703+37859dup	XP_011541856.1:n.1703+37855_1703+37859dup
XM_011543555.1:c.1646+37855_1646+37859dup	XP_011541857.1:n.1646+37855_1646+37859dup
XM_011543556.1:c.1646+37855_1646+37859dup	XP_011541858.1:n.1646+37855_1646+37859dup
XM_011543559.1:c.1704-13415_1704-13411dup	XP_011541861.1:n.1704-13415_1704-13411dup
XM_011543560.1:c.1349+37855_1349+37859dup	XP_011541862.1:n.1349+37855_1349+37859dup
XM_011543564.1:c.1456-65817_1456-65813dup	XP_011541866.1:n.1456-65817_1456-65813dup
XM_011543565.1:c.1456-76084_1456-76080dup	XP_011541867.1:n.1456-76084_1456-76080dup
XM_011543566.1:c.1205+37855_1205+37859dup	XP_011541868.1:n.1205+37855_1205+37859dup
XM_011543568.1:c.1102-65817_1102-65813dup	XP_011541870.1:n.1102-65817_1102-65813dup
XM_011543569.1:c.824+37855_824+37859dup	XP_011541871.1:n.824+37855_824+37859dup
XR_948284.1:n.2551+37855_2551+37859dup
XR_948285.1:n.2304-60632_2304-60628dup
XR_948286.1:n.2403+16879_2403+16883dup
XR_948287.1:n.2302+77714_2302+77718dup
XM_006714670.3:c.1703+37855_1703+37859dup	XP_006714733.1:n.1703+37855_1703+37859dup
XM_011543552.2:c.1703+37855_1703+37859dup	XP_011541854.1:n.1703+37855_1703+37859dup
XM_011543553.2:c.1703+37855_1703+37859dup	XP_011541855.1:n.1703+37855_1703+37859dup
XM_011543555.2:c.1646+37855_1646+37859dup	XP_011541857.1:n.1646+37855_1646+37859dup
XM_011543556.2:c.1646+37855_1646+37859dup	XP_011541858.1:n.1646+37855_1646+37859dup
XM_011543559.2:c.1704-13415_1704-13411dup	XP_011541861.1:n.1704-13415_1704-13411dup
XM_011543560.2:c.1349+37855_1349+37859dup	XP_011541862.1:n.1349+37855_1349+37859dup
XM_011543564.3:c.1456-65817_1456-65813dup	XP_011541866.1:n.1456-65817_1456-65813dup
XM_011543565.3:c.1456-76084_1456-76080dup	XP_011541867.1:n.1456-76084_1456-76080dup
XM_011543566.2:c.1205+37855_1205+37859dup	XP_011541868.1:n.1205+37855_1205+37859dup
XM_017009707.1:c.1205+37855_1205+37859dup	XP_016865196.1:n.1205+37855_1205+37859dup
XM_024446149.1:c.1456-65817_1456-65813dup	XP_024301917.1:n.1456-65817_1456-65813dup
XR_001742181.1:n.2565+37855_2565+37859dup
XR_001742182.1:n.2316+77714_2316+77718dup
XR_948284.2:n.2566+37855_2566+37859dup
XR_948285.2:n.2318-60632_2318-60628dup
XR_948287.2:n.2316+77714_2316+77718dup
NM_001039763.4:c.1703+37855_1703+37859dup MANE Select	NP_001034852.3:n.1703+37855_1703+37859dup