Canonical Allele Identifier: CA608437583

Gene: TMEM132C

Linked Data

• gnomAD v2: 12-129095057-TAG-T
• gnomAD v3: 12-128610512-TAG-T
• gnomAD v4: 12-128610512-TAG-T
• MyVariant Identifiers: chr12:g.129095058_129095059del (hg19) ; chr12:g.128610513_128610514del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128610513_128610514del , CM000674.2:g.128610513_128610514del	GRCh38
NC_000012.11:g.129095058_129095059del , CM000674.1:g.129095058_129095059del	GRCh37
NC_000012.10:g.127661011_127661012del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.1122-5639_1122-5638del MANE Select	ENSP00000410852.2:n.1122-5639_1122-5638del
ENST00000435159.2:c.1122-5639_1122-5638del	ENSP00000410852.2:n.1122-5639_1122-5638del
NM_001136103.2:c.1122-5639_1122-5638del	NP_001129575.2:n.1122-5639_1122-5638del
XM_011538998.1:c.1062-5639_1062-5638del	XP_011537300.1:n.1062-5639_1062-5638del
XM_011538998.2:c.1062-5639_1062-5638del	XP_011537300.1:n.1062-5639_1062-5638del
XR_001748922.1:n.1355-5639_1355-5638del
NM_001136103.3:c.1122-5639_1122-5638del MANE Select	NP_001129575.2:n.1122-5639_1122-5638del
NM_001387058.1:c.1062-5639_1062-5638del	NP_001373987.1:n.1062-5639_1062-5638del