Canonical Allele Identifier: CA2532072060

Gene: TMEM132C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128702046C>G , CM000674.2:g.128702046C>G	GRCh38
NC_000012.11:g.129186591C>G , CM000674.1:g.129186591C>G	GRCh37
NC_000012.10:g.127752544C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.2122-3044C>G MANE Select	ENSP00000410852.2:n.2122-3044C>G
ENST00000435159.2:c.2122-3044C>G	ENSP00000410852.2:n.2122-3044C>G
NM_001136103.2:c.2122-3044C>G	NP_001129575.2:n.2122-3044C>G
XM_011538998.1:c.2062-3044C>G	XP_011537300.1:n.2062-3044C>G
XM_011538998.2:c.2062-3044C>G	XP_011537300.1:n.2062-3044C>G
XR_001748922.1:n.2355-2606C>G
NM_001136103.3:c.2122-3044C>G MANE Select	NP_001129575.2:n.2122-3044C>G
NM_001387058.1:c.2062-3044C>G	NP_001373987.1:n.2062-3044C>G