Canonical Allele Identifier: CA2071351076
Gene: TMEM132C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128701708_128701709delinsGC , CM000674.2:g.128701708_128701709delinsGC GRCh38
NC_000012.11:g.129186253_129186254delinsGC , CM000674.1:g.129186253_129186254delinsGC GRCh37
NC_000012.10:g.127752206_127752207delinsGC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000435159.3:c.2122-3382_2122-3381delinsGC MANE Select ENSP00000410852.2:n.2122-3382_2122-3381de...
ENST00000435159.2:c.2122-3382_2122-3381delinsGC ENSP00000410852.2:n.2122-3382_2122-3381de...
NM_001136103.2:c.2122-3382_2122-3381delinsGC NP_001129575.2:n.2122-3382_2122-3381delin...
XM_011538998.1:c.2062-3382_2062-3381delinsGC XP_011537300.1:n.2062-3382_2062-3381delin...
XM_011538998.2:c.2062-3382_2062-3381delinsGC XP_011537300.1:n.2062-3382_2062-3381delin...
XR_001748922.1:n.2355-2944_2355-2943delinsGC
NM_001136103.3:c.2122-3382_2122-3381delinsGC MANE Select NP_001129575.2:n.2122-3382_2122-3381delin...
NM_001387058.1:c.2062-3382_2062-3381delinsGC NP_001373987.1:n.2062-3382_2062-3381delin...