Canonical Allele Identifier: CA654979310
Gene: TMEM132C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128701656T>G , CM000674.2:g.128701656T>G GRCh38
NC_000012.11:g.129186201T>G , CM000674.1:g.129186201T>G GRCh37
NC_000012.10:g.127752154T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000435159.3:c.2122-3434T>G MANE Select ENSP00000410852.2:n.2122-3434T>G
ENST00000435159.2:c.2122-3434T>G ENSP00000410852.2:n.2122-3434T>G
NM_001136103.2:c.2122-3434T>G NP_001129575.2:n.2122-3434T>G
XM_011538998.1:c.2062-3434T>G XP_011537300.1:n.2062-3434T>G
XM_011538998.2:c.2062-3434T>G XP_011537300.1:n.2062-3434T>G
XR_001748922.1:n.2355-2996T>G
NM_001136103.3:c.2122-3434T>G MANE Select NP_001129575.2:n.2122-3434T>G
NM_001387058.1:c.2062-3434T>G NP_001373987.1:n.2062-3434T>G