Canonical Allele Identifier: CA2797947542

Gene: TMEM132C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128610368_128610370del , CM000674.2:g.128610368_128610370del	GRCh38
NC_000012.11:g.129094913_129094915del , CM000674.1:g.129094913_129094915del	GRCh37
NC_000012.10:g.127660866_127660868del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.1122-5784_1122-5782del MANE Select	ENSP00000410852.2:n.1122-5784_1122-5782del
ENST00000435159.2:c.1122-5784_1122-5782del	ENSP00000410852.2:n.1122-5784_1122-5782del
NM_001136103.2:c.1122-5784_1122-5782del	NP_001129575.2:n.1122-5784_1122-5782del
XM_011538998.1:c.1062-5784_1062-5782del	XP_011537300.1:n.1062-5784_1062-5782del
XM_011538998.2:c.1062-5784_1062-5782del	XP_011537300.1:n.1062-5784_1062-5782del
XR_001748922.1:n.1355-5784_1355-5782del
NM_001136103.3:c.1122-5784_1122-5782del MANE Select	NP_001129575.2:n.1122-5784_1122-5782del
NM_001387058.1:c.1062-5784_1062-5782del	NP_001373987.1:n.1062-5784_1062-5782del