Canonical Allele Identifier: CA2071351072
Gene: TMEM132C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128701699T= , CM000674.2:g.128701699T= GRCh38
NC_000012.11:g.129186244T= , CM000674.1:g.129186244T= GRCh37
NC_000012.10:g.127752197T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000435159.3:c.2122-3391T= MANE Select ENSP00000410852.2:n.2122-3391T=
ENST00000435159.2:c.2122-3391T= ENSP00000410852.2:n.2122-3391T=
NM_001136103.2:c.2122-3391T= NP_001129575.2:n.2122-3391T=
XM_011538998.1:c.2062-3391T= XP_011537300.1:n.2062-3391T=
XM_011538998.2:c.2062-3391T= XP_011537300.1:n.2062-3391T=
XR_001748922.1:n.2355-2953T=
NM_001136103.3:c.2122-3391T= MANE Select NP_001129575.2:n.2122-3391T=
NM_001387058.1:c.2062-3391T= NP_001373987.1:n.2062-3391T=