Canonical Allele Identifier: CA685188273

Gene: TMEM132C

Linked Data

• dbSNP Id: rs1491306754
• gnomAD v3: 12-128701900-T-TTC
• gnomAD v4: 12-128701900-T-TTC
• MyVariant Identifiers: chr12:g.129186445_129186446insTC (hg19) ; chr12:g.128701900_128701901insTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128701901_128701902insCT , CM000674.2:g.128701901_128701902insCT	GRCh38
NC_000012.11:g.129186446_129186447insCT , CM000674.1:g.129186446_129186447insCT	GRCh37
NC_000012.10:g.127752399_127752400insCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.2122-3189_2122-3188insCT MANE Select	ENSP00000410852.2:n.2122-3189_2122-3188insCT
ENST00000435159.2:c.2122-3189_2122-3188insCT	ENSP00000410852.2:n.2122-3189_2122-3188insCT
NM_001136103.2:c.2122-3189_2122-3188insCT	NP_001129575.2:n.2122-3189_2122-3188insCT
XM_011538998.1:c.2062-3189_2062-3188insCT	XP_011537300.1:n.2062-3189_2062-3188insCT
XM_011538998.2:c.2062-3189_2062-3188insCT	XP_011537300.1:n.2062-3189_2062-3188insCT
XR_001748922.1:n.2355-2751_2355-2750insCT
NM_001136103.3:c.2122-3189_2122-3188insCT MANE Select	NP_001129575.2:n.2122-3189_2122-3188insCT
NM_001387058.1:c.2062-3189_2062-3188insCT	NP_001373987.1:n.2062-3189_2062-3188insCT