Canonical Allele Identifier: CA919205117

Gene: TMEM132C

Linked Data

• dbSNP Id: rs1566019446

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128701901_128701902insCTTT , CM000674.2:g.128701901_128701902insCTTT	GRCh38
NC_000012.11:g.129186446_129186447insCTTT , CM000674.1:g.129186446_129186447insCTTT	GRCh37
NC_000012.10:g.127752399_127752400insCTTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.2122-3189_2122-3188insCTTT MANE Select	ENSP00000410852.2:n.2122-3189_2122-3188insCTTT
ENST00000435159.2:c.2122-3189_2122-3188insCTTT	ENSP00000410852.2:n.2122-3189_2122-3188insCTTT
NM_001136103.2:c.2122-3189_2122-3188insCTTT	NP_001129575.2:n.2122-3189_2122-3188insCTTT
XM_011538998.1:c.2062-3189_2062-3188insCTTT	XP_011537300.1:n.2062-3189_2062-3188insCTTT
XM_011538998.2:c.2062-3189_2062-3188insCTTT	XP_011537300.1:n.2062-3189_2062-3188insCTTT
XR_001748922.1:n.2355-2751_2355-2750insCTTT
NM_001136103.3:c.2122-3189_2122-3188insCTTT MANE Select	NP_001129575.2:n.2122-3189_2122-3188insCTTT
NM_001387058.1:c.2062-3189_2062-3188insCTTT	NP_001373987.1:n.2062-3189_2062-3188insCTTT