Canonical Allele Identifier: CA2071351152

Gene: TMEM132C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128701888_128701889delinsCG , CM000674.2:g.128701888_128701889delinsCG	GRCh38
NC_000012.11:g.129186433_129186434delinsCG , CM000674.1:g.129186433_129186434delinsCG	GRCh37
NC_000012.10:g.127752386_127752387delinsCG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.2122-3202_2122-3201delinsCG MANE Select	ENSP00000410852.2:n.2122-3202_2122-3201delinsCG
ENST00000435159.2:c.2122-3202_2122-3201delinsCG	ENSP00000410852.2:n.2122-3202_2122-3201delinsCG
NM_001136103.2:c.2122-3202_2122-3201delinsCG	NP_001129575.2:n.2122-3202_2122-3201delinsCG
XM_011538998.1:c.2062-3202_2062-3201delinsCG	XP_011537300.1:n.2062-3202_2062-3201delinsCG
XM_011538998.2:c.2062-3202_2062-3201delinsCG	XP_011537300.1:n.2062-3202_2062-3201delinsCG
XR_001748922.1:n.2355-2764_2355-2763delinsCG
NM_001136103.3:c.2122-3202_2122-3201delinsCG MANE Select	NP_001129575.2:n.2122-3202_2122-3201delinsCG
NM_001387058.1:c.2062-3202_2062-3201delinsCG	NP_001373987.1:n.2062-3202_2062-3201delinsCG