Canonical Allele Identifier: CA953171178
Gene: TMEM132C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128610507_128610509del , CM000674.2:g.128610507_128610509del GRCh38
NC_000012.11:g.129095052_129095054del , CM000674.1:g.129095052_129095054del GRCh37
NC_000012.10:g.127661005_127661007del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000435159.3:c.1122-5645_1122-5643del MANE Select ENSP00000410852.2:n.1122-5645_1122-5643del
ENST00000435159.2:c.1122-5645_1122-5643del ENSP00000410852.2:n.1122-5645_1122-5643del
NM_001136103.2:c.1122-5645_1122-5643del NP_001129575.2:n.1122-5645_1122-5643del
XM_011538998.1:c.1062-5645_1062-5643del XP_011537300.1:n.1062-5645_1062-5643del
XM_011538998.2:c.1062-5645_1062-5643del XP_011537300.1:n.1062-5645_1062-5643del
XR_001748922.1:n.1355-5645_1355-5643del
NM_001136103.3:c.1122-5645_1122-5643del MANE Select NP_001129575.2:n.1122-5645_1122-5643del
NM_001387058.1:c.1062-5645_1062-5643del NP_001373987.1:n.1062-5645_1062-5643del