Canonical Allele Identifier: CA2603964677
Gene: TMEM132C HGNC NCBI

Linked Data

dbSNP Id: rs2135660891
gnomAD v3: 12-128701679-CT-C
gnomAD v4: 12-128701679-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128701680del , CM000674.2:g.128701680del GRCh38
NC_000012.11:g.129186225del , CM000674.1:g.129186225del GRCh37
NC_000012.10:g.127752178del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000435159.3:c.2122-3410del MANE Select ENSP00000410852.2:n.2122-3410del
ENST00000435159.2:c.2122-3410del ENSP00000410852.2:n.2122-3410del
NM_001136103.2:c.2122-3410del NP_001129575.2:n.2122-3410del
XM_011538998.1:c.2062-3410del XP_011537300.1:n.2062-3410del
XM_011538998.2:c.2062-3410del XP_011537300.1:n.2062-3410del
XR_001748922.1:n.2355-2972del
NM_001136103.3:c.2122-3410del MANE Select NP_001129575.2:n.2122-3410del
NM_001387058.1:c.2062-3410del NP_001373987.1:n.2062-3410del
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