Canonical Allele Identifier: CA245297332

Gene: TMEM132C

Linked Data

• dbSNP Id: rs964221570
• gnomAD v3: 12-128701482-T-TACA
• gnomAD v4: 12-128701482-T-TACA
• MyVariant Identifiers: chr12:g.129186027_129186028insACA (hg19) ; chr12:g.128701482_128701483insACA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128701483_128701485dup , CM000674.2:g.128701483_128701485dup	GRCh38
NC_000012.11:g.129186028_129186030dup , CM000674.1:g.129186028_129186030dup	GRCh37
NC_000012.10:g.127751981_127751983dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.2122-3607_2122-3605dup MANE Select	ENSP00000410852.2:n.2122-3607_2122-3605dup
ENST00000435159.2:c.2122-3607_2122-3605dup	ENSP00000410852.2:n.2122-3607_2122-3605dup
NM_001136103.2:c.2122-3607_2122-3605dup	NP_001129575.2:n.2122-3607_2122-3605dup
XM_011538998.1:c.2062-3607_2062-3605dup	XP_011537300.1:n.2062-3607_2062-3605dup
XM_011538998.2:c.2062-3607_2062-3605dup	XP_011537300.1:n.2062-3607_2062-3605dup
XR_001748922.1:n.2355-3169_2355-3167dup
NM_001136103.3:c.2122-3607_2122-3605dup MANE Select	NP_001129575.2:n.2122-3607_2122-3605dup
NM_001387058.1:c.2062-3607_2062-3605dup	NP_001373987.1:n.2062-3607_2062-3605dup