Canonical Allele Identifier: CA2071351023
Gene: TMEM132C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128701586A= , CM000674.2:g.128701586A= GRCh38
NC_000012.11:g.129186131A= , CM000674.1:g.129186131A= GRCh37
NC_000012.10:g.127752084A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000435159.3:c.2122-3504A= MANE Select ENSP00000410852.2:n.2122-3504A=
ENST00000435159.2:c.2122-3504A= ENSP00000410852.2:n.2122-3504A=
NM_001136103.2:c.2122-3504A= NP_001129575.2:n.2122-3504A=
XM_011538998.1:c.2062-3504A= XP_011537300.1:n.2062-3504A=
XM_011538998.2:c.2062-3504A= XP_011537300.1:n.2062-3504A=
XR_001748922.1:n.2355-3066A=
NM_001136103.3:c.2122-3504A= MANE Select NP_001129575.2:n.2122-3504A=
NM_001387058.1:c.2062-3504A= NP_001373987.1:n.2062-3504A=