Canonical Allele Identifier: CA953171165
Gene: TMEM132C HGNC NCBI

Linked Data

gnomAD v3: 12-128610504-TGA-T
gnomAD v4: 12-128610504-TGA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128610505_128610506del , CM000674.2:g.128610505_128610506del GRCh38
NC_000012.11:g.129095050_129095051del , CM000674.1:g.129095050_129095051del GRCh37
NC_000012.10:g.127661003_127661004del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000435159.3:c.1122-5647_1122-5646del MANE Select ENSP00000410852.2:n.1122-5647_1122-5646del
ENST00000435159.2:c.1122-5647_1122-5646del ENSP00000410852.2:n.1122-5647_1122-5646del
NM_001136103.2:c.1122-5647_1122-5646del NP_001129575.2:n.1122-5647_1122-5646del
XM_011538998.1:c.1062-5647_1062-5646del XP_011537300.1:n.1062-5647_1062-5646del
XM_011538998.2:c.1062-5647_1062-5646del XP_011537300.1:n.1062-5647_1062-5646del
XR_001748922.1:n.1355-5647_1355-5646del
NM_001136103.3:c.1122-5647_1122-5646del MANE Select NP_001129575.2:n.1122-5647_1122-5646del
NM_001387058.1:c.1062-5647_1062-5646del NP_001373987.1:n.1062-5647_1062-5646del
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