Canonical Allele Identifier: CA953171195
Gene: TMEM132C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128610517_128610519del , CM000674.2:g.128610517_128610519del GRCh38
NC_000012.11:g.129095062_129095064del , CM000674.1:g.129095062_129095064del GRCh37
NC_000012.10:g.127661015_127661017del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000435159.3:c.1122-5635_1122-5633del MANE Select ENSP00000410852.2:n.1122-5635_1122-5633del
ENST00000435159.2:c.1122-5635_1122-5633del ENSP00000410852.2:n.1122-5635_1122-5633del
NM_001136103.2:c.1122-5635_1122-5633del NP_001129575.2:n.1122-5635_1122-5633del
XM_011538998.1:c.1062-5635_1062-5633del XP_011537300.1:n.1062-5635_1062-5633del
XM_011538998.2:c.1062-5635_1062-5633del XP_011537300.1:n.1062-5635_1062-5633del
XR_001748922.1:n.1355-5635_1355-5633del
NM_001136103.3:c.1122-5635_1122-5633del MANE Select NP_001129575.2:n.1122-5635_1122-5633del
NM_001387058.1:c.1062-5635_1062-5633del NP_001373987.1:n.1062-5635_1062-5633del