Canonical Allele Identifier: CA685188304

Gene: TMEM132C

Linked Data

• dbSNP Id: rs1491084144
• gnomAD v3: 12-128701916-T-TA
• gnomAD v4: 12-128701916-T-TA
• MyVariant Identifiers: chr12:g.129186461_129186462insA (hg19) ; chr12:g.128701916_128701917insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128701916_128701917insA , CM000674.2:g.128701916_128701917insA	GRCh38
NC_000012.11:g.129186461_129186462insA , CM000674.1:g.129186461_129186462insA	GRCh37
NC_000012.10:g.127752414_127752415insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.2122-3174_2122-3173insA MANE Select	ENSP00000410852.2:n.2122-3174_2122-3173insA
ENST00000435159.2:c.2122-3174_2122-3173insA	ENSP00000410852.2:n.2122-3174_2122-3173insA
NM_001136103.2:c.2122-3174_2122-3173insA	NP_001129575.2:n.2122-3174_2122-3173insA
XM_011538998.1:c.2062-3174_2062-3173insA	XP_011537300.1:n.2062-3174_2062-3173insA
XM_011538998.2:c.2062-3174_2062-3173insA	XP_011537300.1:n.2062-3174_2062-3173insA
XR_001748922.1:n.2355-2736_2355-2735insA
NM_001136103.3:c.2122-3174_2122-3173insA MANE Select	NP_001129575.2:n.2122-3174_2122-3173insA
NM_001387058.1:c.2062-3174_2062-3173insA	NP_001373987.1:n.2062-3174_2062-3173insA