Canonical Allele Identifier: CA2560194799
Gene: TMEM132C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128701563_128701564insAGT , CM000674.2:g.128701563_128701564insAGT GRCh38
NC_000012.11:g.129186108_129186109insAGT , CM000674.1:g.129186108_129186109insAGT GRCh37
NC_000012.10:g.127752061_127752062insAGT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000435159.3:c.2122-3527_2122-3526insAGT MANE Select ENSP00000410852.2:n.2122-3527_2122-3526in...
ENST00000435159.2:c.2122-3527_2122-3526insAGT ENSP00000410852.2:n.2122-3527_2122-3526in...
NM_001136103.2:c.2122-3527_2122-3526insAGT NP_001129575.2:n.2122-3527_2122-3526insAG...
XM_011538998.1:c.2062-3527_2062-3526insAGT XP_011537300.1:n.2062-3527_2062-3526insAG...
XM_011538998.2:c.2062-3527_2062-3526insAGT XP_011537300.1:n.2062-3527_2062-3526insAG...
XR_001748922.1:n.2355-3089_2355-3088insAGT
NM_001136103.3:c.2122-3527_2122-3526insAGT MANE Select NP_001129575.2:n.2122-3527_2122-3526insAG...
NM_001387058.1:c.2062-3527_2062-3526insAGT NP_001373987.1:n.2062-3527_2062-3526insAG...