Canonical Allele Identifier: CA608437587

Gene: TMEM132C

Linked Data

• gnomAD v2: 12-129095066-AGT-A
• gnomAD v3: 12-128610521-AGT-A
• gnomAD v4: 12-128610521-AGT-A
• MyVariant Identifiers: chr12:g.129095067_129095068del (hg19) ; chr12:g.128610522_128610523del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128610522_128610523del , CM000674.2:g.128610522_128610523del	GRCh38
NC_000012.11:g.129095067_129095068del , CM000674.1:g.129095067_129095068del	GRCh37
NC_000012.10:g.127661020_127661021del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.1122-5630_1122-5629del MANE Select	ENSP00000410852.2:n.1122-5630_1122-5629del
ENST00000435159.2:c.1122-5630_1122-5629del	ENSP00000410852.2:n.1122-5630_1122-5629del
NM_001136103.2:c.1122-5630_1122-5629del	NP_001129575.2:n.1122-5630_1122-5629del
XM_011538998.1:c.1062-5630_1062-5629del	XP_011537300.1:n.1062-5630_1062-5629del
XM_011538998.2:c.1062-5630_1062-5629del	XP_011537300.1:n.1062-5630_1062-5629del
XR_001748922.1:n.1355-5630_1355-5629del
NM_001136103.3:c.1122-5630_1122-5629del MANE Select	NP_001129575.2:n.1122-5630_1122-5629del
NM_001387058.1:c.1062-5630_1062-5629del	NP_001373987.1:n.1062-5630_1062-5629del