Canonical Allele Identifier: CA125314769
Gene: TMEM232 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.110523120A>G , CM000667.2:g.110523120A>G GRCh38
NC_000005.9:g.109858821A>G , CM000667.1:g.109858821A>G GRCh37
NC_000005.8:g.109886720A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000455884.7:c.1703+5468T>C MANE Select ENSP00000401477.2:n.1703+5468T>C
ENST00000455884.6:c.1703+5468T>C ENSP00000401477.2:n.1703+5468T>C
ENST00000508571.6:n.1018+45327T>C
ENST00000512003.7:c.*997+45327T>C ENSP00000427785.2:n.*997+45327T>C
ENST00000515518.6:n.1375+45327T>C
NM_001039763.3:c.1703+5468T>C NP_001034852.3:n.1703+5468T>C
XM_006714670.2:c.1703+5468T>C XP_006714733.1:n.1703+5468T>C
XM_011543552.1:c.1703+5468T>C XP_011541854.1:n.1703+5468T>C
XM_011543553.1:c.1703+5468T>C XP_011541855.1:n.1703+5468T>C
XM_011543554.1:c.1703+5468T>C XP_011541856.1:n.1703+5468T>C
XM_011543555.1:c.1646+5468T>C XP_011541857.1:n.1646+5468T>C
XM_011543556.1:c.1646+5468T>C XP_011541858.1:n.1646+5468T>C
XM_011543557.1:c.1703+5468T>C XP_011541859.1:n.1703+5468T>C
XM_011543558.1:c.1703+5468T>C XP_011541860.1:n.1703+5468T>C
XM_011543559.1:c.1703+5468T>C XP_011541861.1:n.1703+5468T>C
XM_011543560.1:c.1349+5468T>C XP_011541862.1:n.1349+5468T>C
XM_011543561.1:c.1456-19458T>C XP_011541863.1:n.1456-19458T>C
XM_011543562.1:c.1456-15409T>C XP_011541864.1:n.1456-15409T>C
XM_011543563.1:c.1456-15409T>C XP_011541865.1:n.1456-15409T>C
XM_011543564.1:c.1455+45327T>C XP_011541866.1:n.1455+45327T>C
XM_011543565.1:c.1455+45327T>C XP_011541867.1:n.1455+45327T>C
XM_011543566.1:c.1205+5468T>C XP_011541868.1:n.1205+5468T>C
XM_011543568.1:c.1101+45327T>C XP_011541870.1:n.1101+45327T>C
XM_011543569.1:c.824+5468T>C XP_011541871.1:n.824+5468T>C
XR_948284.1:n.2551+5468T>C
XR_948285.1:n.2303+45327T>C
XR_948286.1:n.2304-15409T>C
XR_948287.1:n.2302+45327T>C
XM_006714670.3:c.1703+5468T>C XP_006714733.1:n.1703+5468T>C
XM_011543552.2:c.1703+5468T>C XP_011541854.1:n.1703+5468T>C
XM_011543553.2:c.1703+5468T>C XP_011541855.1:n.1703+5468T>C
XM_011543555.2:c.1646+5468T>C XP_011541857.1:n.1646+5468T>C
XM_011543556.2:c.1646+5468T>C XP_011541858.1:n.1646+5468T>C
XM_011543557.2:c.1703+5468T>C XP_011541859.1:n.1703+5468T>C
XM_011543559.2:c.1703+5468T>C XP_011541861.1:n.1703+5468T>C
XM_011543560.2:c.1349+5468T>C XP_011541862.1:n.1349+5468T>C
XM_011543561.2:c.1456-19458T>C XP_011541863.1:n.1456-19458T>C
XM_011543563.2:c.1456-15409T>C XP_011541865.1:n.1456-15409T>C
XM_011543564.3:c.1455+45327T>C XP_011541866.1:n.1455+45327T>C
XM_011543565.3:c.1455+45327T>C XP_011541867.1:n.1455+45327T>C
XM_011543566.2:c.1205+5468T>C XP_011541868.1:n.1205+5468T>C
XM_017009705.2:c.1703+5468T>C XP_016865194.1:n.1703+5468T>C
XM_017009706.2:c.1456-15409T>C XP_016865195.1:n.1456-15409T>C
XM_017009707.1:c.1205+5468T>C XP_016865196.1:n.1205+5468T>C
XM_024446149.1:c.1455+45327T>C XP_024301917.1:n.1455+45327T>C
XR_001742181.1:n.2565+5468T>C
XR_001742182.1:n.2316+45327T>C
XR_948284.2:n.2566+5468T>C
XR_948285.2:n.2317+45327T>C
XR_948287.2:n.2316+45327T>C
NM_001039763.4:c.1703+5468T>C MANE Select NP_001034852.3:n.1703+5468T>C
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