Canonical Allele Identifier: CA608437586

Gene: TMEM132C

Linked Data

• gnomAD v2: 12-129095064-A-AT
• gnomAD v3: 12-128610519-A-AT
• gnomAD v4: 12-128610519-A-AT
• MyVariant Identifiers: chr12:g.129095064_129095065insT (hg19) ; chr12:g.128610519_128610520insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128610519_128610520insT , CM000674.2:g.128610519_128610520insT	GRCh38
NC_000012.11:g.129095064_129095065insT , CM000674.1:g.129095064_129095065insT	GRCh37
NC_000012.10:g.127661017_127661018insT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.1122-5633_1122-5632insT MANE Select	ENSP00000410852.2:n.1122-5633_1122-5632insT
ENST00000435159.2:c.1122-5633_1122-5632insT	ENSP00000410852.2:n.1122-5633_1122-5632insT
NM_001136103.2:c.1122-5633_1122-5632insT	NP_001129575.2:n.1122-5633_1122-5632insT
XM_011538998.1:c.1062-5633_1062-5632insT	XP_011537300.1:n.1062-5633_1062-5632insT
XM_011538998.2:c.1062-5633_1062-5632insT	XP_011537300.1:n.1062-5633_1062-5632insT
XR_001748922.1:n.1355-5633_1355-5632insT
NM_001136103.3:c.1122-5633_1122-5632insT MANE Select	NP_001129575.2:n.1122-5633_1122-5632insT
NM_001387058.1:c.1062-5633_1062-5632insT	NP_001373987.1:n.1062-5633_1062-5632insT