Canonical Allele Identifier: CA2071351188

Gene: TMEM132C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128701922_128701924delinsCAG , CM000674.2:g.128701922_128701924delinsCAG	GRCh38
NC_000012.11:g.129186467_129186469delinsCAG , CM000674.1:g.129186467_129186469delinsCAG	GRCh37
NC_000012.10:g.127752420_127752422delinsCAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.2122-3168_2122-3166delinsCAG MANE Select	ENSP00000410852.2:n.2122-3168_2122-3166delinsCAG
ENST00000435159.2:c.2122-3168_2122-3166delinsCAG	ENSP00000410852.2:n.2122-3168_2122-3166delinsCAG
NM_001136103.2:c.2122-3168_2122-3166delinsCAG	NP_001129575.2:n.2122-3168_2122-3166delinsCAG
XM_011538998.1:c.2062-3168_2062-3166delinsCAG	XP_011537300.1:n.2062-3168_2062-3166delinsCAG
XM_011538998.2:c.2062-3168_2062-3166delinsCAG	XP_011537300.1:n.2062-3168_2062-3166delinsCAG
XR_001748922.1:n.2355-2730_2355-2728delinsCAG
NM_001136103.3:c.2122-3168_2122-3166delinsCAG MANE Select	NP_001129575.2:n.2122-3168_2122-3166delinsCAG
NM_001387058.1:c.2062-3168_2062-3166delinsCAG	NP_001373987.1:n.2062-3168_2062-3166delinsCAG