Canonical Allele Identifier: CA953178813
Gene: TMEM132C HGNC NCBI

Linked Data

gnomAD v3: 12-128701917-TGA-T
gnomAD v4: 12-128701917-TGA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128701920_128701921del , CM000674.2:g.128701920_128701921del GRCh38
NC_000012.11:g.129186465_129186466del , CM000674.1:g.129186465_129186466del GRCh37
NC_000012.10:g.127752418_127752419del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000435159.3:c.2122-3170_2122-3169del MANE Select ENSP00000410852.2:n.2122-3170_2122-3169del
ENST00000435159.2:c.2122-3170_2122-3169del ENSP00000410852.2:n.2122-3170_2122-3169del
NM_001136103.2:c.2122-3170_2122-3169del NP_001129575.2:n.2122-3170_2122-3169del
XM_011538998.1:c.2062-3170_2062-3169del XP_011537300.1:n.2062-3170_2062-3169del
XM_011538998.2:c.2062-3170_2062-3169del XP_011537300.1:n.2062-3170_2062-3169del
XR_001748922.1:n.2355-2732_2355-2731del
NM_001136103.3:c.2122-3170_2122-3169del MANE Select NP_001129575.2:n.2122-3170_2122-3169del
NM_001387058.1:c.2062-3170_2062-3169del NP_001373987.1:n.2062-3170_2062-3169del
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