Canonical Allele Identifier: CA125310708
Gene: TMEM232 HGNC NCBI

Linked Data

dbSNP Id: rs10067777

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.110490595A>G , CM000667.2:g.110490595A>G GRCh38
NC_000005.9:g.109826296A>G , CM000667.1:g.109826296A>G GRCh37
NC_000005.8:g.109854195A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000455884.7:c.1703+37993T>C MANE Select ENSP00000401477.2:p.=
ENST00000455884.6:c.1703+37993T>C ENSP00000401477.2:p.=
ENST00000508571.6:n.1018+77852T>C
ENST00000512003.7:c.*998-65679T>C ENSP00000427785.2:p.=
ENST00000515518.6:n.1376-65679T>C
NM_001039763.3:c.1703+37993T>C NP_001034852.3:p.=
XM_006714670.2:c.1703+37993T>C XP_006714733.1:p.=
XM_011543552.1:c.1703+37993T>C XP_011541854.1:p.=
XM_011543553.1:c.1703+37993T>C XP_011541855.1:p.=
XM_011543554.1:c.1703+37993T>C XP_011541856.1:p.=
XM_011543555.1:c.1646+37993T>C XP_011541857.1:p.=
XM_011543556.1:c.1646+37993T>C XP_011541858.1:p.=
XM_011543559.1:c.1704-13277T>C XP_011541861.1:p.=
XM_011543560.1:c.1349+37993T>C XP_011541862.1:p.=
XM_011543564.1:c.1456-65679T>C XP_011541866.1:p.=
XM_011543565.1:c.1456-75946T>C XP_011541867.1:p.=
XM_011543566.1:c.1205+37993T>C XP_011541868.1:p.=
XM_011543568.1:c.1102-65679T>C XP_011541870.1:p.=
XM_011543569.1:c.824+37993T>C XP_011541871.1:p.=
XR_948284.1:n.2551+37993T>C
XR_948285.1:n.2304-60494T>C
XR_948286.1:n.2403+17017T>C
XR_948287.1:n.2302+77852T>C
XM_006714670.3:c.1703+37993T>C XP_006714733.1:p.=
XM_011543552.2:c.1703+37993T>C XP_011541854.1:p.=
XM_011543553.2:c.1703+37993T>C XP_011541855.1:p.=
XM_011543555.2:c.1646+37993T>C XP_011541857.1:p.=
XM_011543556.2:c.1646+37993T>C XP_011541858.1:p.=
XM_011543559.2:c.1704-13277T>C XP_011541861.1:p.=
XM_011543560.2:c.1349+37993T>C XP_011541862.1:p.=
XM_011543564.3:c.1456-65679T>C XP_011541866.1:p.=
XM_011543565.3:c.1456-75946T>C XP_011541867.1:p.=
XM_011543566.2:c.1205+37993T>C XP_011541868.1:p.=
XM_017009707.1:c.1205+37993T>C XP_016865196.1:p.=
XM_024446149.1:c.1456-65679T>C XP_024301917.1:p.=
XR_001742181.1:n.2565+37993T>C
XR_001742182.1:n.2316+77852T>C
XR_948284.2:n.2566+37993T>C
XR_948285.2:n.2318-60494T>C
XR_948287.2:n.2316+77852T>C
NM_001039763.4:c.1703+37993T>C MANE Select NP_001034852.3:p.=