Canonical Allele Identifier: CA2071351198

Gene: TMEM132C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128701943_128701949delinsCAGCTGG , CM000674.2:g.128701943_128701949delinsCAGCTGG	GRCh38
NC_000012.11:g.129186488_129186494delinsCAGCTGG , CM000674.1:g.129186488_129186494delinsCAGCTGG	GRCh37
NC_000012.10:g.127752441_127752447delinsCAGCTGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.2122-3147_2122-3141delinsCAGCTGG MANE Select	ENSP00000410852.2:n.2122-3147_2122-3141delinsCAGCTGG
ENST00000435159.2:c.2122-3147_2122-3141delinsCAGCTGG	ENSP00000410852.2:n.2122-3147_2122-3141delinsCAGCTGG
NM_001136103.2:c.2122-3147_2122-3141delinsCAGCTGG	NP_001129575.2:n.2122-3147_2122-3141delinsCAGCTGG
XM_011538998.1:c.2062-3147_2062-3141delinsCAGCTGG	XP_011537300.1:n.2062-3147_2062-3141delinsCAGCTGG
XM_011538998.2:c.2062-3147_2062-3141delinsCAGCTGG	XP_011537300.1:n.2062-3147_2062-3141delinsCAGCTGG
XR_001748922.1:n.2355-2709_2355-2703delinsCAGCTGG
NM_001136103.3:c.2122-3147_2122-3141delinsCAGCTGG MANE Select	NP_001129575.2:n.2122-3147_2122-3141delinsCAGCTGG
NM_001387058.1:c.2062-3147_2062-3141delinsCAGCTGG	NP_001373987.1:n.2062-3147_2062-3141delinsCAGCTGG