Canonical Allele Identifier: CA2797949127

Gene: TMEM132C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128701899_128701900del , CM000674.2:g.128701899_128701900del	GRCh38
NC_000012.11:g.129186444_129186445del , CM000674.1:g.129186444_129186445del	GRCh37
NC_000012.10:g.127752397_127752398del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.2122-3191_2122-3190del MANE Select	ENSP00000410852.2:n.2122-3191_2122-3190del
ENST00000435159.2:c.2122-3191_2122-3190del	ENSP00000410852.2:n.2122-3191_2122-3190del
NM_001136103.2:c.2122-3191_2122-3190del	NP_001129575.2:n.2122-3191_2122-3190del
XM_011538998.1:c.2062-3191_2062-3190del	XP_011537300.1:n.2062-3191_2062-3190del
XM_011538998.2:c.2062-3191_2062-3190del	XP_011537300.1:n.2062-3191_2062-3190del
XR_001748922.1:n.2355-2753_2355-2752del
NM_001136103.3:c.2122-3191_2122-3190del MANE Select	NP_001129575.2:n.2122-3191_2122-3190del
NM_001387058.1:c.2062-3191_2062-3190del	NP_001373987.1:n.2062-3191_2062-3190del