Canonical Allele Identifier: CA953171168
Gene: TMEM132C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128610505_128610508del , CM000674.2:g.128610505_128610508del GRCh38
NC_000012.11:g.129095050_129095053del , CM000674.1:g.129095050_129095053del GRCh37
NC_000012.10:g.127661003_127661006del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000435159.3:c.1122-5647_1122-5644del MANE Select ENSP00000410852.2:n.1122-5647_1122-5644del
ENST00000435159.2:c.1122-5647_1122-5644del ENSP00000410852.2:n.1122-5647_1122-5644del
NM_001136103.2:c.1122-5647_1122-5644del NP_001129575.2:n.1122-5647_1122-5644del
XM_011538998.1:c.1062-5647_1062-5644del XP_011537300.1:n.1062-5647_1062-5644del
XM_011538998.2:c.1062-5647_1062-5644del XP_011537300.1:n.1062-5647_1062-5644del
XR_001748922.1:n.1355-5647_1355-5644del
NM_001136103.3:c.1122-5647_1122-5644del MANE Select NP_001129575.2:n.1122-5647_1122-5644del
NM_001387058.1:c.1062-5647_1062-5644del NP_001373987.1:n.1062-5647_1062-5644del
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